BiobaseTypes 0.0.2.2 → 0.2.1.0
raw patch · 28 files changed
Files
- Biobase/Types/Accession.hs +128/−0
- Biobase/Types/BioSequence.hs +409/−0
- Biobase/Types/Bitscore.hs +94/−0
- Biobase/Types/Codon.hs +20/−0
- Biobase/Types/Convert.hs +0/−36
- Biobase/Types/Energy.hs +79/−35
- Biobase/Types/Evalue.hs +56/−0
- Biobase/Types/Index.hs +116/−0
- Biobase/Types/Index/Type.hs +117/−0
- Biobase/Types/Location.hs +253/−0
- Biobase/Types/Names.hs +143/−0
- Biobase/Types/Names/Internal.hs +36/−0
- Biobase/Types/Partition.hs +0/−84
- Biobase/Types/Position.hs +163/−0
- Biobase/Types/ReadingFrame.hs +54/−0
- Biobase/Types/Ring.hs +0/−22
- Biobase/Types/Score.hs +0/−48
- Biobase/Types/Shape.hs +202/−0
- Biobase/Types/Strand.hs +147/−0
- Biobase/Types/Structure.hs +225/−0
- Biobase/Types/Taxonomy.hs +71/−0
- BiobaseTypes.cabal +137/−24
- DP/Backtraced/BioSequence.hs +3/−0
- DP/Backtraced/Codon.hs +46/−0
- LICENSE +24/−669
- README.md +21/−0
- changelog.md +55/−0
- tests/properties.hs +134/−0
+ Biobase/Types/Accession.hs view
@@ -0,0 +1,128 @@++-- | Accession numbers. These /numbers/ are not really numbers because they+-- they are made up of alphanumeric characters.++module Biobase.Types.Accession where++import Control.DeepSeq+import Data.Aeson+import Data.Binary+import Data.Char (isLetter)+import Data.Hashable (Hashable)+import Data.Ix (Ix)+import Data.Serialize+import Data.Serialize.Text+import Data.String+import Data.String.Conversions (ConvertibleStrings(..), cs)+import Data.String.Conversions.Monomorphic (toST, fromST)+import Data.Text.Binary+import Data.Text (Text, span, length)+import GHC.Generics (Generic)+import Prelude hiding (length,span)++++-- * 'Accession' with phantom types.+--+-- <http://www.ncbi.nlm.nih.gov/Sequin/acc.html>+--+-- <http://www.uniprot.org/help/accession_numbers>+--+-- <http://en.wikipedia.org/wiki/Accession_number_%28bioinformatics%29>++-- | The accession number is a unique identifier in bioinformatics.+--+-- Depending on the source, accession numbers follow different alphanumeric+-- formats! While letters-than-numbers is quite common, swissprot uses+-- a mix. Hence, we just use a text string as accession.+--+-- A phantom type is provided to enable type safety annotations. Helper+-- functions provide smart construction from the @Accession@ tagged generic+-- type.++newtype Accession t = Accession { _getAccession :: Text }+ deriving (Eq,Ord,Read,Show,Generic)++-- | Generate an accession with an explicit phantom type: @accession'+-- Nucleotide "Bla"@ has type @:: Accession Nucleotide@.++accession' :: ConvertibleStrings s Text => t -> s -> Accession t+accession' t = Accession . toST++-- | Generate an accession when the type @Accession t@ is clear from the+-- context.++accession :: ConvertibleStrings s Text => s -> Accession t+accession = Accession . toST+{-# Inline accession #-}++-- | Retag an accession++retagAccession :: Accession f -> Accession t+retagAccession = Accession . _getAccession+{-# Inline retagAccession #-}++instance IsString (Accession t) where+ fromString = accession+ {-# Inline fromString #-}++instance Binary (Accession t)+instance FromJSON (Accession t)+instance Hashable (Accession t)+instance Serialize (Accession t)+instance ToJSON (Accession t)+instance NFData (Accession t)++++-- * Phantom types. All with an excliti data constructor to guide+-- 'accession''.++-- ** NCBI phantom types++-- | nucleotide sequence++data Nucleotide = Nucleotide++-- | protein sequence++data Protein = Protein++-- ** Rfam phantom types+--+-- The format is RFxxxxx, PFxxxxx, or CLxxxxx.++-- | Tag as being a clan.++data Clan = Clan++-- | Tag as being a Pfam model.++data Pfam = Pfam++-- | Tag as being an Rfam model. Used for Stockholm and CM files.++data Rfam = Rfam++-- | Species have an accession number, too.++data Species = Species++++-- * Helper functions++-- | Guess the type of accession number. Returns @Nothing@ if unknown+-- structure.++guessAccessionType :: Accession t -> Maybe Text+guessAccessionType (Accession a) = case (length l, length d) of+ (1,5) -> Just "Nucleotide"+ (2,6) -> Just "Nucleotide"+ (3,5) -> Just "Protein"+ (3,k) | 8<= k && k<= 10 -> Just "WGS"+ (5,7) -> Just "MGA"+ _ -> Nothing+ where (l,d) = span isLetter a++
+ Biobase/Types/BioSequence.hs view
@@ -0,0 +1,409 @@++-- | Abstraction over bio sequences encoded as one-ascii character as one+-- symbol. We phantom-type the exact bio-sequence type and provide type classes+-- that act on known types.+--+-- Unknown bio sequences should be tagged with @Void@.+--+-- TODO give (lens) usage examples++module Biobase.Types.BioSequence where++import Control.DeepSeq+import Control.Lens+import Data.ByteString.Char8 (ByteString)+import Data.Char (ord,chr,toUpper)+import Data.Data (Data)+import Data.Hashable+import Data.Typeable (Typeable)+import Data.Void+import GHC.Exts (IsString(..))+import GHC.Generics (Generic)+import qualified Data.ByteString.Char8 as BS+import qualified Data.ByteString.UTF8 as BSU+import qualified Streaming.Prelude as SP+import qualified Streaming as S+import qualified Streaming.Internal as SI+import qualified Test.QuickCheck as TQ+import Test.QuickCheck (Arbitrary(..))+import Data.Coerce+import Debug.Trace++import Biobase.Types.Strand+import qualified Biobase.Types.Index as BTI+import Data.Info++++-- * Lens operations on biosequences++{-+class BioSeqLenses b where+ -- | Lens into the first @k@ characters.+ bsTake :: Int -> Lens' b b+ -- | Lens into the last @k@ characters+ bsTakeEnd :: Int -> Lens' b b+ -- | Lens into all but the first @k@ characters+ bsDrop :: Int -> Lens' b b+ -- | Lens into all but the last @k@ characters+ bsDropEnd :: Int -> Lens' b b+ -- | Lens that splits at a position+ bsSplitAt :: Int -> Lens' b (b,b)+ -- | length of this biosequence+ bsLength :: Getter b Int+-}++-- * Sequence identifiers++newtype SequenceIdentifier (which :: k) = SequenceIdentifier { _sequenceIdentifier :: ByteString }+ deriving stock (Data, Typeable, Generic, Eq, Ord, Read, Show)+makeWrapped ''SequenceIdentifier+makePrisms ''SequenceIdentifier++instance NFData (SequenceIdentifier w)++instance IsString (SequenceIdentifier w) where+ fromString = SequenceIdentifier . BSU.fromString++++-- * Bio-Sequences++data RNA++data DNA++data XNA++data AA++++-- |+-- TODO provide extended annotation information on biosequences, too!++newtype BioSequence (which :: k) = BioSequence {_bioSequence :: ByteString}+ deriving stock (Data, Typeable, Generic, Eq, Ord, Read, Show)+ deriving newtype (Semigroup)+makeWrapped ''BioSequence+makePrisms ''BioSequence+makeLenses ''BioSequence++instance Hashable (BioSequence (which :: k))++instance NFData (BioSequence w)++type instance Index (BioSequence w) = Int++type instance IxValue (BioSequence w) = Char++instance Ixed (BioSequence w) where+ ix k = _BioSequence . ix k . iso (chr . fromIntegral) (fromIntegral . ord)+ {-# Inline ix #-}++deriving newtype instance Reversing (BioSequence w)++instance IsString (BioSequence Void) where+ fromString = BioSequence . BS.pack++instance Info (BioSequence w) where+ info (BioSequence s)+ | BS.length s <= 18 = BS.unpack s+ | otherwise = BS.unpack h ++ ".." ++ BS.unpack l+ where (h,tl) = BS.splitAt 9 s+ (_,l ) = BS.splitAt (BS.length tl-9) tl++{-+instance BioSeqLenses (BioSequence w) where+ {-# Inline bsTake #-}+ bsTake k = lens (over _BioSequence (BS.take k)) (\old new -> new <> over _BioSequence (BS.drop k) old)+ {-# Inline bsTakeEnd #-}+ bsTakeEnd k = lens (over _BioSequence (\s -> BS.drop (BS.length s -k) s)) (\old new -> over _BioSequence (\s -> BS.take (BS.length s-k) s) old <> new)+ {-# Inline bsLength #-}+ bsLength = _BioSequence.to BS.length+ {-# Inline bsDrop #-}+ bsDrop k = lens (over _BioSequence (BS.drop k)) (\old new -> over _BioSequence (BS.take k) old <> new)+ {-# Inline bsDropEnd #-}+ bsDropEnd k = lens (over _BioSequence (\s -> BS.take (BS.length s -k) s)) (\old new -> over _BioSequence (\s -> BS.take (BS.length s-k) s) old <> new)+ {-# Inline bsSplitAt #-}+ bsSplitAt k = lens (\b -> (view (bsTake k) b, view (bsDrop k) b)) (\old (h,t) -> h <> t)+-}++++-- * RNA++-- |+--+-- TODO write that converts explicitly++mkRNAseq :: ByteString -> BioSequence RNA+mkRNAseq = BioSequence . BS.map go . BS.map toUpper+ where go x | x `elem` acgu = x+ | otherwise = 'N'+ acgu :: String+ acgu = "ACGU"++instance IsString (BioSequence RNA) where+ fromString = mkRNAseq . BS.pack++instance Arbitrary (BioSequence RNA) where+ arbitrary = do+ k ← TQ.choose (0,30)+ xs ← TQ.vectorOf k $ TQ.elements "ACGU"+ return . BioSequence $ BS.pack xs+ shrink = shrinkBioSequence++shrinkBioSequence (BioSequence b) = fmap BioSequence+ [ let (l,BS.drop 1 -> r) = BS.splitAt k b+ in BS.append l r | k <- [0 .. BS.length b -1] ]+++-- * DNA++mkDNAseq :: ByteString -> (BioSequence DNA)+mkDNAseq = BioSequence . BS.map go . BS.map toUpper+ where go x | x `elem` acgt = x+ | otherwise = 'N'+ acgt :: String+ acgt = "ACGT"++instance IsString (BioSequence DNA) where+ fromString = mkDNAseq . BS.pack++instance Arbitrary (BioSequence DNA) where+ arbitrary = do+ k ← TQ.choose (0,100)+ xs ← TQ.vectorOf k $ TQ.elements "ACGT"+ return . BioSequence $ BS.pack xs+ shrink = view (to shrink)++++-- * XNA++mkXNAseq :: ByteString -> (BioSequence XNA)+mkXNAseq = BioSequence . BS.map go . BS.map toUpper+ where go x | x `elem` acgtu = x+ | otherwise = 'N'+ acgtu :: String+ acgtu = "ACGTU"++instance IsString (BioSequence XNA) where+ fromString = mkXNAseq . BS.pack++instance Arbitrary (BioSequence XNA) where+ arbitrary = do+ k ← TQ.choose (0,100)+ xs ← TQ.vectorOf k $ TQ.elements "ACGTU"+ return . BioSequence $ BS.pack xs+ shrink = view (to shrink)++++-- * Amino acid sequences++mkAAseq :: ByteString -> (BioSequence AA)+mkAAseq = BioSequence . BS.map go . BS.map toUpper+ where go x | x `elem` aas = x+ | otherwise = 'X'+ aas :: String+ aas = "ARNDCEQGHILKMFPSTWYVUO"++instance IsString (BioSequence AA) where+ fromString = mkAAseq . BS.pack++instance Arbitrary (BioSequence AA) where+ arbitrary = do+ k ← TQ.choose (0,100)+ xs ← TQ.vectorOf k $ TQ.elements "ARNDCEQGHILKMFPSTWYVUO"+ return . BioSequence $ BS.pack xs+ shrink = view (to shrink)++++{-++-- * A window into a longer sequence with prefix/suffix information.++-- | Phantom-typed over two types, the type @w@ of the identifier, which can be+-- descriptive ("FirstInput") and the second type, identifying what kind of+-- sequence types we are dealing with. Finally, the third type provides+-- location information and should be location or streamed location.++data BioSequenceWindow w ty loc = BioSequenceWindow+ { _bswIdentifier :: !(SequenceIdentifier w)+ -- ^ Identifier for this window. Typically some fasta identifier+ , _bswPrefix :: !(BioSequence ty)+ , _bswInfix :: !(BioSequence ty)+ , _bswSuffix :: !(BioSequence ty)+ , _bswInfixLocation :: !loc+ -- ^ Location of the infix sequence+ }+ deriving (Data, Typeable, Generic, Eq, Ord, Read, Show)+makeLenses ''BioSequenceWindow++-- | Lens into the full sequence. May not change the sequence length++bswSequence :: Lens (BioSequenceWindow w ty loc) (BioSequenceWindow w ty' loc) (BioSequence ty) (BioSequence ty')+{-# Inlinable bswSequence #-}+bswSequence = lens (\w -> _bswPrefix w <> _bswInfix w <> _bswSuffix w)+ (\w bs -> let (p,is) = bs^.bsSplitAt (w^.bswPrefix.bsLength)+ (i,s ) = is^.bsSplitAt (w^.bswInfix.bsLength)+ in w { _bswPrefix = p, _bswInfix = i, _bswSuffix = s } )++-- | Get the position of the whole sequence++bswLocation :: ModifyLocation loc => Getter (BioSequenceWindow w ty loc) loc+{-# Inlinable bswLocation #-}+bswLocation = to $ \w -> locMoveLeftEnd (w^.bswPrefix.bsLength.to negate)+ . locMoveRightEnd (w^.bswSuffix.bsLength) $ w^.bswInfixLocation++bswRetagW :: BioSequenceWindow w ty loc -> BioSequenceWindow v ty loc+{-# Inlinable bswRetagW #-}+bswRetagW = over bswIdentifier coerce++instance NFData loc => NFData (BioSequenceWindow w ty loc)++instance (Reversing loc) => Reversing (BioSequenceWindow w ty loc) where+ {-# Inlinable reversing #-}+ reversing bsw = bsw+ & bswPrefix .~ (bsw^.bswSuffix.reversed)+ & bswSuffix .~ (bsw^.bswPrefix.reversed)+ & bswInfix .~ (bsw^.bswInfix.reversed)+ & bswInfixLocation .~ (bsw^.bswInfixLocation.reversed)++++-- | Provides an informative string indicating the current window being worked on. Requires length+-- of pretty string requested. Not for computers, but for logging what is being worked on. Should be+-- one line at most, not produce line breaks.+--+-- @...PFX [Start] IFX...IFX [End] SFX ...@+--+-- TODO possibly be better as a @Doc@ for prettier printing.++instance Info (BioSequenceWindow w ty loc) where+ info bsw = "todo: info bsw"++-}++++-- * DNA/RNA++-- | Simple case translation from @U@ to @T@. with upper and lower-case+-- awareness.++rna2dna :: Char -> Char+rna2dna = \case+ 'U' -> 'T'+ 'u' -> 't'+ x -> x+{-# Inline rna2dna #-}++-- | Single character RNA complement.++rnaComplement :: Char -> Char+rnaComplement = \case+ 'A' -> 'U'+ 'a' -> 'u'+ 'C' -> 'G'+ 'c' -> 'g'+ 'G' -> 'C'+ 'g' -> 'c'+ 'U' -> 'A'+ 'u' -> 'a'+ x -> x+{-# Inline rnaComplement #-}++-- | Simple case translation from @T@ to @U@ with upper- and lower-case+-- awareness.++dna2rna :: Char -> Char+dna2rna = \case+ 'T' -> 'U'+ 't' -> 'u'+ x -> x+{-# Inline dna2rna #-}++-- | Single character DNA complement.++dnaComplement :: Char -> Char+dnaComplement = \case+ 'A' -> 'T'+ 'a' -> 't'+ 'C' -> 'G'+ 'c' -> 'g'+ 'G' -> 'C'+ 'g' -> 'c'+ 'T' -> 'A'+ 't' -> 'a'+ x -> x+{-# Inline dnaComplement #-}++++-- | Transcribes a DNA sequence into an RNA sequence. Note that 'transcribe' is+-- actually very generic. We just define its semantics to be that of+-- biomolecular transcription.+--+-- 'transcribe' makes the assumption that, given @DNA -> RNA@, we transcribe+-- the coding strand.+-- <http://hyperphysics.phy-astr.gsu.edu/hbase/Organic/transcription.html>+--+-- @@ DNAseq "ACGT" ^. transcribe == RNAseq "ACGU" RNAseq "ACGU" ^. transcribe+-- == DNAseq "ACGT" RNAseq "ACGU" ^. from transcribe :: DNAseq == DNAseq "ACGT"+-- @@++class Transcribe f where+ type TranscribeTo f :: *+ transcribe :: Iso' f (TranscribeTo f)++-- | Transcribe a DNA sequence into an RNA sequence. This does not @reverse@+-- the sequence!++instance Transcribe (BioSequence DNA) where+ type TranscribeTo (BioSequence DNA) = (BioSequence RNA)+ transcribe = iso (over _BioSequence (BS.map dna2rna)) (over _BioSequence (BS.map rna2dna))+ {-# Inline transcribe #-}++-- | Transcribe a RNA sequence into an DNA sequence. This does not @reverse@+-- the sequence!++instance Transcribe (BioSequence RNA) where+ type TranscribeTo (BioSequence RNA) = (BioSequence DNA)+ transcribe = from transcribe+ {-# Inline transcribe #-}++++-- | The complement of a biosequence.++class Complement f where+ complement :: Iso' f f++instance Complement (BioSequence DNA) where+ {-# Inline complement #-}+ complement = let f = (over _BioSequence (BS.map dnaComplement))+ {-# Inline f #-}+ in iso f f++instance Complement (BioSequence RNA) where+ {-# Inline complement #-}+ complement = let f = (over _BioSequence (BS.map rnaComplement))+ {-# Inline f #-}+ in iso f f++{-+instance (Complement (BioSequence ty)) => Complement (BioSequenceWindow w ty k) where+ {-# Inline complement #-}+ complement = let f = over bswPrefix (view complement) . over bswInfix (view complement) . over bswSuffix (view complement)+ {-# Inline f #-}+ in iso f f+-}++reverseComplement :: (Complement f, Reversing f) => Iso' f f+{-# Inline reverseComplement #-}+reverseComplement = reversed . complement+
+ Biobase/Types/Bitscore.hs view
@@ -0,0 +1,94 @@++-- | Bit scores as used by different algorithms in bioinformatics,+-- linguistics, and probably elsewhere.+--+-- Basically, the base-2 logarithm of the probability of the input given+-- the model vs the probability of the input given the null model.+--+-- @+-- S = log_2 (P(seq|model) / P(seq|null))+-- @+--++module Biobase.Types.Bitscore where++import Control.DeepSeq+import Data.Aeson+import Data.Binary+import Data.Default+import Data.Hashable (Hashable)+import Data.Primitive.Types+import Data.Serialize+import Data.Vector.Unboxed.Base+import Data.Vector.Unboxed.Deriving+import GHC.Generics (Generic)+import qualified Data.Vector.Generic as VG+import qualified Data.Vector.Generic.Mutable as VGM+import qualified Data.Vector.Unboxed as VU++import Algebra.Structure.Semiring+import Numeric.Limits++++-- | Bit score; behaves like a double (deriving Num). In particular, the+-- algebraic operations behave as expected @Bitscore a + Bitscore b ==+-- Bitscore (a+b)@.+--+-- Currently geared towards use as in @Infernal@ and @HMMER@.+--+-- Infernal users guide, p.42: log-odds score in log_2 (aka bits).++newtype Bitscore = Bitscore { getBitscore :: Double }+ deriving stock (Eq,Ord,Read,Show,Generic)+ deriving newtype (Num,Fractional)++instance Semiring Bitscore where+ plus = (+)+ times = (*)+ zero = 0+ one = 1+ {-# Inline plus #-}+ {-# Inline times #-}+ {-# Inline zero #-}+ {-# Inline one #-}++instance Binary Bitscore+instance FromJSON Bitscore+instance Hashable Bitscore+instance Serialize Bitscore+instance ToJSON Bitscore+instance NFData Bitscore++deriving newtype instance NumericLimits Bitscore++derivingUnbox "Bitscore"+ [t| Bitscore -> Double |] [| getBitscore |] [| Bitscore |]++-- | A default bitscore of "-infinity", but with @10-1@ wiggle room.+--+-- TODO Check out the different "defaults" Infernal uses++instance Default Bitscore where+ def = Bitscore minFinite / 100+ {-# Inline def #-}++-- | Given a null model and a probability, calculate the corresponding+-- 'BitScore'.+--+-- TODO @x<=epsilon@ ?++prob2Score :: Double -> Double -> Bitscore+prob2Score null x+ | x==0 = minFinite / 100+ | otherwise = Bitscore $ log (x/null) / log 2+{-# Inline prob2Score #-}++-- | Given a null model and a 'BitScore' return the corresponding probability.++score2Prob :: Double -> Bitscore -> Double+score2Prob null (Bitscore x)+ | x <= minFinite / 100 = 0+ | otherwise = null * exp (x * log 2)+{-# Inline score2Prob #-}+
+ Biobase/Types/Codon.hs view
@@ -0,0 +1,20 @@++module Biobase.Types.Codon where++import Control.Lens+import GHC.Generics (Generic)++++-- | A single codon.+--+-- TODO needs to go into its own place++data Codon c = Codon !c !c !c+ deriving (Eq,Ord,Read,Show,Generic,Functor,Foldable,Traversable)++instance Field1 (Codon c) (Codon c) c c+instance Field2 (Codon c) (Codon c) c c+instance Field3 (Codon c) (Codon c) c c+instance Each (Codon c) (Codon c') c c'+
− Biobase/Types/Convert.hs
@@ -1,36 +0,0 @@-{-# LANGUAGE MultiParamTypeClasses #-}---- | Provides a converting function between different types. Most useful--- conversions are instanced here.--module Biobase.Types.Convert where--import Biobase.Types.Ring-import Biobase.Types.Energy-import Biobase.Types.Score-import Biobase.Types.Partition------ | How to convert between different values.--class Convert a b c where- convert :: a -> b -> c------ | From (Gibbs free) energy to partition function values.------ TODO temperature is running around here: move to some library later on--newtype Kelvin = Kelvin {unKelvin :: Double}--constR = undefined--instance Convert Kelvin Energy Partition where- convert (Kelvin k) (Energy a) = Partition . exp $ (fromIntegral $ negate a) / (constR * k)---- | From log-odd scores to partition function.---- instance Convert Temperature Score Partition where--- convert (Score a) = Partition . exp $ (fromIntegral $ neg a) / (constR * constT)
Biobase/Types/Energy.hs view
@@ -1,51 +1,95 @@-{-# LANGUAGE StandaloneDeriving #-}-{-# LANGUAGE MultiParamTypeClasses #-}-{-# LANGUAGE GeneralizedNewtypeDeriving #-} +-- | Different types of energies and conversion between.+--+-- TODO enthalpy+-- TODO entropy+ module Biobase.Types.Energy where -import qualified Data.Vector.Unboxed as VU-import qualified Data.Vector.Generic as VG-import qualified Data.Vector.Generic.Mutable as VGM-import Data.Primitive.Types+import Control.DeepSeq+import Control.Lens+import Data.Aeson (FromJSON, ToJSON)+import Data.Binary (Binary)+import Data.Data+import Data.Default+import Data.Hashable+import GHC.Real+import Data.Serialize (Serialize)+import Data.Vector.Unboxed.Deriving+import GHC.Generics -import Biobase.Types.Ring+import Algebra.Structure.Semiring+import Numeric.Discretized+import Numeric.Limits --- | Some default instances. Left out the Num one, so that you have to--- explicitly instanciate if you want to go around the Ring structure.+-- | Gibbs free energy change.+--+-- For RNA structure, the change in energy from the unfolded structure to+-- the given structure.+--+-- In units of @kcal / mol@.+--+-- TODO shall we phantom-type the actual units? -newtype Energy = Energy {unEnergy :: Int}- deriving (Show, Read, Eq, Ord)+newtype DG = DG { dG :: Double }+ deriving (Eq,Ord,Num,Fractional,Read,Show,Generic,Data,Typeable)+makeLenses ''DG +derivingUnbox "DG"+ [t| DG -> Double |] [| dG |] [| DG |] +instance Hashable DG+instance Binary DG+instance Serialize DG+instance FromJSON DG+instance ToJSON DG+instance NFData DG --- | Ring operations over Energy values.+deriving instance NumericLimits DG+deriving instance NumericEpsilon DG -instance Ring Energy where- (Energy a) .+. (Energy b) = Energy $ a `min` b- {-# INLINE (.+.) #-}- (Energy a) .*. (Energy b) = Energy $ a + b- {-# INLINE (.*.) #-}- (Energy a) .^. k = Energy $ a * k- {-# INLINE (.^.) #-}- (Energy a) .^^. k = Energy . round $ fromIntegral a * k- {-# INLINE (.^^.) #-}- neg (Energy a) = Energy $ negate a- {-# INLINE neg #-}- one = Energy 0- {-# INLINE one #-}- zero = Energy 10000000- {-# INLINE zero #-}- isZero (Energy a) = a >= 1000000- {-# INLINE isZero #-}+instance Default DG where+ def = maxFinite / 100+ {-# Inline def #-} --- * Vector instances.+-- | Discretized @DG@. -deriving instance VGM.MVector VU.MVector Energy-deriving instance VG.Vector VU.Vector Energy-deriving instance VU.Unbox Energy-deriving instance Prim Energy+newtype DDG = DDG { dDG ∷ Discretized (1 :% 100) }+ deriving (Eq,Ord,Num,Read,Generic,Real,Enum)++instance Show DDG where+ show (DDG e) = show e++ddg2Int :: DDG -> Int+ddg2Int (DDG (Discretized e)) = e++derivingUnbox "DDG"+ [t| DDG -> Int |] [| getDiscretized . dDG |] [| DDG . Discretized |]++instance Semiring DDG where+ plus (DDG x) (DDG y) = DDG $ min x y+ times (DDG x) (DDG y) = DDG $ x `plus` y+ zero = DDG maxFinite+ one = DDG zero+ {-# Inline plus #-}+ {-# Inline times #-}+ {-# Inline zero #-}+ {-# Inline one #-}++--instance Hashable DeltaDekaGibbs+--instance Binary DeltaDekaGibbs+--instance Serialize DeltaDekaGibbs+--instance FromJSON DeltaDekaGibbs+--instance ToJSON DeltaDekaGibbs+--instance NFData DeltaDekaGibbs+--+--deriving instance NumericLimits DeltaDekaGibbs+--+--instance Default DeltaDekaGibbs where+-- def = maxFinite `div` 100+-- {-# Inline def #-}+--
+ Biobase/Types/Evalue.hs view
@@ -0,0 +1,56 @@++-- | Encode the number of hits to expect. This is typically dependent on+-- some "database size". Evalues are bounded by @[0,infinity)@.+--+-- TODO Evalues close to zero are more interesting. We should strongly+-- consider log-conversion here.++module Biobase.Types.Evalue where++import Control.DeepSeq+import Control.Lens+import Data.Aeson+import Data.Binary+import Data.Default+import Data.Hashable (Hashable)+import Data.Primitive.Types+import Data.Serialize+import Data.Vector.Unboxed.Base+import Data.Vector.Unboxed.Deriving+import GHC.Generics (Generic)+import qualified Data.Vector.Generic as VG+import qualified Data.Vector.Generic.Mutable as VGM+import qualified Data.Vector.Unboxed as VU++import Numeric.Limits++++-- | Type-safe wrapper for e-values.++newtype Evalue = Evalue { getEvalue :: Double }+ deriving (Eq,Ord,Read,Show,Num,Generic)+makeWrapped ''Evalue++instance Binary Evalue+instance FromJSON Evalue+instance Hashable Evalue+instance Serialize Evalue+instance ToJSON Evalue+instance NFData Evalue++derivingUnbox "Evalue"+ [t| Evalue -> Double |] [| getEvalue |] [| Evalue |]++-- | By default, we expect no hits.++instance Default Evalue where+ def = Evalue 0+ {-# Inline def #-}++instance NumericLimits Evalue where+ maxFinite = Evalue maxFinite+ minFinite = Evalue 0+ {-# Inline maxFinite #-}+ {-# Inline minFinite #-}+
+ Biobase/Types/Index.hs view
@@ -0,0 +1,116 @@++-- | Biological sequence data is oftentimes indexed either @0-@ or+-- @1-@based. The @Index@ type developed provides static guarantees that+-- there is no confusion what index is in use.+--+-- This module does not export the ctor @Index@. If you want to (unsafely)+-- use it, import @Biobase.Types.Index.Type@ directly. Use @fromInt0@ to+-- make clear that you count from 0 and transform to an @Index t@. I.e.+-- @fromInt0 0 :: Index 1@ yields the lowest 1-base index.+--+-- Note that internally, every lowest index starts at @0 :: Int@.++module Biobase.Types.Index+ ( module Biobase.Types.Index+ , getIndex+ , index+ , maybeIndex+ , Index+ ) where++import Data.Coerce+import Data.Proxy+import GHC.TypeLits+import Text.Printf++import Biobase.Types.Index.Type -- hiding (getIndex)+import qualified Biobase.Types.Index.Type as IT++++-- | Uses 'index' to guarantee that the 'Index' is ok.++checkIndex :: forall t . KnownNat t => Index t -> Index t+checkIndex i@(Index z)+ | z >= 0 = i+ | otherwise = error $ printf "%d < Index %d\n" (z+n) n+ where n :: Int = fromIntegral $ natVal (Proxy :: Proxy t)+{-# Inline checkIndex #-}++-- | Re-Index an index of type @Index n@ as @Index m@. This is always safe,+-- as @0 :: Index 0@ gives @1 :: Index 1@ for example. I.e. valid indices+-- become valid indices.++reIndex ∷ Index n → Index m+{-# Inline reIndex #-}+reIndex = coerce+--reIndex :: forall n m . (KnownNat n, KnownNat m) => Index n -> Index m+--reIndex (Index i) = Index $ i - n + m+-- where n = fromIntegral $ natVal (Proxy :: Proxy n)+-- m = fromIntegral $ natVal (Proxy :: Proxy m)++-- | Helper function that allows @addition@ of an 'Index' and an 'Int',+-- with the 'Int' on the right.++(+.) :: forall t . KnownNat t => Index t -> Int -> Index t+(+.) i n = checkIndex $ unsafePlus i n+{-# Inline (+.) #-}++-- | Helper function that allows @subtraction@ of an 'Index' and an 'Int',+-- with the 'Int' on the right.++(-.) :: forall t . KnownNat t => Index t -> Int -> Index t+(-.) i n = checkIndex $ unsafePlus i (negate n)+{-# Inline (-.) #-}++-- | Unsafe plus.++unsafePlus :: forall t . KnownNat t => Index t -> Int -> Index t+unsafePlus i n = Index $ IT.getIndex i + n+{-# Inline unsafePlus #-}++-- | Delta between two 'Index' points.++delta :: forall t . KnownNat t => Index t -> Index t -> Int+delta (Index i) (Index j) = abs $ i - j+{-# Inline delta #-}++toInt ∷ forall t . KnownNat t ⇒ Index t → Int+{-# Inline toInt #-}+toInt i = IT.getIndex i + (fromIntegral $ natVal (Proxy ∷ Proxy t))++-- | Return the index as an @Int@-style index that is zero-based.++toInt0 :: forall t . KnownNat t => Index t -> Int+toInt0 = IT.getIndex+{-# Inline toInt0 #-}++-- | Return the index as an @Int@-style index that is one-based.++toInt1 ∷ forall t . KnownNat t ⇒ Index t → Int+{-# Inline toInt1 #-}+toInt1 = (+1) . toInt0++fromInt1 ∷ forall t . KnownNat t ⇒ Int → Index t+{-# Inline fromInt1 #-}+fromInt1 = fromInt0 . (subtract 1)++-- | As an index from an @Int@-style zero-based one.+--+-- TODO We might want to check that the argument is @[0..]@.++fromInt0 :: forall t . KnownNat t => Int -> Index t+fromInt0 i+ | i >= 0 = Index i+ | otherwise = error "fromInt0 needs an Int >= 0"+ where t = fromIntegral $ natVal (Proxy :: Proxy t)+{-# Inline fromInt0 #-}++-- | Zero-based indices.++type I0 = Index 0++-- | One-based indices.++type I1 = Index 1+
+ Biobase/Types/Index/Type.hs view
@@ -0,0 +1,117 @@++module Biobase.Types.Index.Type where++import Control.Applicative ((<$>))+import Control.DeepSeq+import Data.Aeson+import Data.Binary+import Data.Data (Data)+import Data.Hashable (Hashable)+import Data.Proxy+import Data.Serialize (Serialize)+import Data.Typeable (Typeable)+import Data.Vector.Fusion.Stream.Monadic (Step(..), flatten)+import Data.Vector.Unboxed.Deriving+import GHC.Generics+import GHC.TypeLits+import qualified Data.Ix as Ix+import qualified Data.Vector.Fusion.Stream.Monadic as SM+import Test.QuickCheck+import Text.Printf++import Data.PrimitiveArray.Index.Class hiding (Index)+import qualified Data.PrimitiveArray.Index.Class as PA++++-- | A linear @Int@-based index type.++newtype Index (t :: Nat) = Index { getIndex :: Int }+ deriving (Show,Read,Eq,Ord,Generic,Ix.Ix,Data,Typeable)++-- | Turn an 'Int' into an 'Index' safely.++index :: forall t . KnownNat t => Int -> Index t+index i = maybe (error $ printf "%d < Index %d\n" i n) id $ maybeIndex i+ where n = natVal (Proxy :: Proxy t)+{-# Inline index #-}++-- | Produce 'Just' and 'Index' or 'Nothing'.++maybeIndex :: forall t . KnownNat t => Int -> Maybe (Index t)+maybeIndex i+ | i >= n = Just . Index $ i - n+ | otherwise = Nothing+ where n = fromIntegral $ natVal (Proxy :: Proxy t)+{-# Inline maybeIndex #-}++instance KnownNat t => Num (Index t) where+ Index a + Index b = error $ show (" Index.(+) not implemented, use (+.)",a,b) -- index $ a + b+ Index a - Index b = error $ show (" Index.(-) not implemented, use (-.)",a,b) -- index $ a - b+ Index a * Index b = error $ show (" Index.(*) not implemented", a,b) -- index $ a * b+ negate = error "Indices are natural numbers"+ abs = id+ signum = index . signum . getIndex+ fromInteger = index . fromIntegral+ {-# Inline fromInteger #-}++instance NFData (Index t) where+ rnf = rnf . getIndex+ {-# Inline rnf #-}++instance Binary (Index t)+instance Serialize (Index t)+instance ToJSON (Index t)+instance FromJSON (Index t)+instance Hashable (Index t)++derivingUnbox "Index"+ [t| forall t . Index t -> Int |] [| getIndex |] [| Index |]++instance forall t . KnownNat t => PA.Index (Index t) where+ newtype LimitType (Index t) = LtIndex Int+ linearIndex (LtIndex k) (Index z) = z+ {-# INLINE linearIndex #-}+ size (LtIndex h) = h + 1+ {-# INLINE size #-}+ inBounds (LtIndex h) (Index x) = 0<=x && x<=h+ {-# INLINE inBounds #-}+ zeroBound = Index 0+ {-# Inline zeroBound #-}+ zeroBound' = LtIndex 0+ {-# Inline zeroBound' #-}+ totalSize (LtIndex k) = [fromIntegral k]+ {-# Inline totalSize #-}+ fromLinearIndex _ = Index+ {-# Inline [0] fromLinearIndex #-}+ showBound (LtIndex k) = ["LtIndex " ++ show k]+ showIndex (Index k) = ["Index " ++ show k]++instance (KnownNat t, IndexStream z) ⇒ IndexStream (z:.Index t) where+ streamUp (ls:..LtIndex lf) (hs:..LtIndex ht) = flatten mk step $ streamUp ls hs+ where mk z = return (z,lf)+ step (z,k)+ | k > ht = return $ Done+ | otherwise = return $ Yield (z:.Index k) (z,k+1)+ {-# Inline [0] mk #-}+ {-# Inline [0] step #-}+ {-# Inline streamUp #-}+ streamDown (ls:..LtIndex lf) (hs:..LtIndex ht) = flatten mk step $ streamDown ls hs+ where mk z = return (z,ht)+ step (z,k)+ | k < lf = return $ Done+ | otherwise = return $ Yield (z:.Index k) (z,k-1)+ {-# Inline [0] mk #-}+ {-# Inline [0] step #-}+ {-# Inline streamDown #-}++instance (KnownNat t) ⇒ IndexStream (Index t) where+ streamUp l h = SM.map (\(Z:.i) -> i) $ streamUp (ZZ:..l) (ZZ:..h)+ {-# INLINE streamUp #-}+ streamDown l h = SM.map (\(Z:.i) -> i) $ streamDown (ZZ:..l) (ZZ:..h)+ {-# INLINE streamDown #-}++instance Arbitrary (Index t) where+ arbitrary = Index <$> arbitrary+ shrink (Index j) = map Index $ shrink j+
+ Biobase/Types/Location.hs view
@@ -0,0 +1,253 @@++-- | Annotate the genomic @Location@ of features or elements. A @Location@ is+-- always contiguous, using strand, 0-based position, and length.+-- Transformation to different systems of annotation is made possible.++module Biobase.Types.Location where++import Control.DeepSeq+import Control.Lens hiding (Index, index)+import Data.Coerce+import Data.Data+import Data.Data.Lens+import GHC.Generics (Generic)+import GHC.TypeNats+import Prelude hiding (length)+import qualified Data.ByteString as BS+import qualified Streaming.Internal as SI+import qualified Streaming.Prelude as SP+import Text.Printf++import Biobase.Types.BioSequence+import Biobase.Types.Index+import Biobase.Types.Position+import Biobase.Types.Strand+import Data.Info+++++-- | Operations on locations.++class ModifyLocation posTy seqTy where+ -- | Append to the left.+ locAppendLeft :: seqTy -> Location i posTy seqTy -> Location i posTy seqTy+ -- | Append to the right.+ locAppendRight :: seqTy -> Location i posTy seqTy -> Location i posTy seqTy+ -- | Split a location.+ locSplitAt :: Int -> Location i posTy seqTy -> (Location i posTy seqTy, Location i posTy seqTy)+ -- | Length of location+ locLength :: Location i posTy seqTy -> Int++locTake k = fst . locSplitAt k++locTakeEnd k loc = let l = locLength loc in snd $ locSplitAt (l-k) loc++locDrop k = snd . locSplitAt k++locDropEnd k loc = let l = locLength loc in fst $ locSplitAt (l-k) loc++locSplitEndAt k loc = let l = locLength loc in locSplitAt (l-k) loc++++data Location ident posTy seqTy = Location+ { _locIdentifier :: !(SequenceIdentifier ident)+ , _locPosition :: !posTy+ , _locSequence :: !seqTy+ }+ deriving stock (Show,Data,Typeable,Generic)+makeLenses ''Location++instance (NFData p, NFData s) => NFData (Location i p s)++retagLocation :: Location i posTy seqTy -> Location j posTy seqTy+{-# Inline retagLocation #-}+retagLocation = over locIdentifier coerce++instance ModifyLocation FwdPosition (BioSequence w) where+ {-# Inline locAppendLeft #-}+ locAppendLeft s loc = let l = s^._BioSequence.to BS.length+ in loc & locSequence %~ (s <>) & locPosition %~ (\p -> if p^.fwdStrand == PlusStrand then p & fwdStart %~ (-. l) else p)+ {-# Inline locAppendRight #-}+ locAppendRight s loc = let l = s^._BioSequence.to BS.length+ in loc & locSequence %~ (<> s) & locPosition %~ (\p -> if p^.fwdStrand == MinusStrand then p & fwdStart %~ (-. l) else p)+ {-# Inline locSplitAt #-}+ locSplitAt k loc =+ let (h',t') = loc^.locSequence._BioSequence.to (BS.splitAt k)+ hl = BS.length h' ; tl = BS.length t'+ h = loc & locSequence._BioSequence .~ h' & locPosition %~ (\p -> if p^.fwdStrand == MinusStrand then p & fwdStart %~ (+. tl) else p)+ t = loc & locSequence._BioSequence .~ t' & locPosition %~ (\p -> if p^.fwdStrand == PlusStrand then p & fwdStart %~ (+. hl) else p)+ in (h,t)+ {-# Inline locLength #-}+ locLength = view (locSequence._BioSequence.to BS.length)++instance ModifyLocation FwdPosition Int where+ {-# Inline locAppendLeft #-}+ locAppendLeft k' loc = let k = max 0 $ min (loc^.locPosition.fwdStart.to toInt0) k' in+ loc & locSequence %~ (+ k) & locPosition %~ (\p -> if p^.fwdStrand == PlusStrand then p & fwdStart %~ (-. k) else p)+ {-# Inline locAppendRight #-}+ locAppendRight k' loc = let k = max 0 $ min (loc^.locPosition.fwdStart.to toInt0) k' in+ loc & locSequence %~ (+ k) & locPosition %~ (\p -> if p^.fwdStrand == MinusStrand then p & fwdStart %~ (-. k) else p)+ {-# Inline locSplitAt #-}+ locSplitAt k loc =+ let h' = max 0 . min k $ locLength loc+ t' = locLength loc - h'+ h = loc & locSequence .~ h' & locPosition %~ (\p -> if p^.fwdStrand == MinusStrand then p & fwdStart %~(+. t') else p)+ t = loc & locSequence .~ t' & locPosition %~ (\p -> if p^.fwdStrand == PlusStrand then p & fwdStart %~ (+. h') else p)+ in (h,t)+ {-# Inline locLength #-}+ locLength = view locSequence++instance Reversing (Location i FwdPosition (BioSequence w)) where+ {-# Inline reversing #-}+ reversing = over (locSequence._BioSequence) BS.reverse . over (locPosition) reversing++instance Complement (BioSequence w) => Complement (Location i FwdPosition (BioSequence w)) where+ {-# Inline complement #-}+ complement = iso f f+ where f = over locSequence (view complement)++instance (Info (BioSequence w)) => Info (Location i FwdPosition (BioSequence w)) where+ info loc = printf "%s %s %s" (loc^.locIdentifier^.to show) (show $ loc^.locPosition) (loc^.locSequence.to info)++-- | Will extract a substring for a given biosequence. It is allowed to hand in partially or not at+-- all overlapping locational information. This will yield empty resulting locations.+--+-- This will convert the @FwdPosition@ strand, which in turn allows dealing with reverse-complement+-- searches.+--+-- @+-- 0123456789+-- 3.3+-- @++subLocation :: Location i FwdPosition (BioSequence w) -> (FwdPosition, Int) -> Location i FwdPosition (BioSequence w)+{-# Inline subLocation #-}+subLocation s (p',l)+ | ss==PlusStrand = locTake l $ locDrop d s+ | ss==MinusStrand = locTakeEnd l $ locDropEnd d s+ where ss = s^.locPosition.fwdStrand+ p = if ss == p'^.fwdStrand then p' else reversing p'+ d = delta (s^.locPosition.fwdStart) (p^.fwdStart)++data PIS i p s = PIS+ { _pisPrefix :: Maybe (Location i p s)+ , _pisInfix :: !(Location i p s)+ , _pisSuffix :: Maybe (Location i p s)+ }+ deriving stock (Show, Data)+makeLenses ''PIS++pis ifx = PIS Nothing ifx Nothing++retagPis :: PIS i p s -> PIS j p s+retagPis (PIS p i s) = PIS (fmap retagLocation p) (retagLocation i) (fmap retagLocation s)++-- | Given a @PIS@, this will return the @substring@ indicated by the location in the 2nd argument.+-- Allows for easy substring extraction, and retains the system of prefix/infix/suffix.+--+-- It is allowed to hand locations that only partially (or not at all) correspond to the @PIS@, but+-- then the resulting @PIS@ will be empty!++subPisLocation :: PIS i FwdPosition (BioSequence w) -> (FwdPosition, Int) -> PIS i FwdPosition (BioSequence w)+{-# Inline subPisLocation #-}+subPisLocation pis loc =+ let f z = subLocation z loc+ in over (pisPrefix._Just) f . over pisInfix f $ over (pisSuffix._Just) f pis++instance (Reversing (Location i FwdPosition (BioSequence w))) => Reversing (PIS i FwdPosition (BioSequence w)) where+ {-# Inline reversing #-}+ reversing pis+ = over (pisPrefix._Just) reversing . over pisInfix reversing . over (pisSuffix._Just) reversing+ . set pisPrefix (pis^.pisSuffix) . set pisSuffix (pis^.pisPrefix) $ pis++instance Complement (BioSequence w) => Complement (PIS i FwdPosition (BioSequence w)) where+ {-# Inline complement #-}+ complement =+ let f = over pisInfix (view complement) . over (pisPrefix._Just) (view complement) . over (pisSuffix._Just) (view complement)+ in iso f f++pisSequence :: Lens (PIS i p (BioSequence s)) (PIS i p (BioSequence t)) (BioSequence s) (BioSequence t)+{-# Inline pisSequence #-}+pisSequence = lens f t where+ v = view (locSequence.bioSequence)+ f (PIS p i s) = BioSequence $ maybe BS.empty v p `BS.append` v i `BS.append` maybe BS.empty v s+ t (PIS p i s) (BioSequence str) =+ let (pfx,ifxsfx) = over _1 BioSequence $ BS.splitAt (maybe 0 (BS.length . v) p) str+ (ifx,sfx ) = over both BioSequence $ BS.splitAt (BS.length $ v i) ifxsfx+ in PIS (set (_Just . locSequence) pfx p) (set locSequence ifx i) (set (_Just . locSequence) sfx s)++++-- | Given a @Location@ with a @BioSequence@, replace the sequence with its length.++locAsLength :: Location i FwdPosition (BioSequence w) -> Location i FwdPosition Int+{-# Inline locAsLength #-}+locAsLength = over locSequence (view (_BioSequence.to BS.length))++++-- | Provides a range in a notation as used by blast, for example. This+-- isomorphism can translate back as well. @FwdLocation - 8 4 ^. blastRange1 ==+-- 9 6 MinusStrand@, since these ranges are 1-based and start and end included.++blastRange1 :: (Location i FwdPosition Int) -> (Int,Int,Strand)+{-# Inline blastRange1 #-}+blastRange1 = f -- iso f t+ where+ f loc =+ let s = loc^.locPosition.fwdStart.to toInt1+ l = loc^.locSequence+ pm = loc^.locPosition.fwdStrand+ in case pm of PlusStrand -> (s,s+l,pm) ; MinusStrand -> (s+l,s,pm)+-- t (x,y,pm) =+-- let s = fromInt1 x+-- l = 1 + abs (x-y)+-- in Location (FwdPosition pm s) l++++-- | For each element, attach the prefix as well. The @Int@ indicates the maximal prefix length to+-- attach.+--+-- @1 2 3 4@ -> @01 12 23 34@+--+-- TODO are we sure this is correct for @MinusStrand@?++attachPrefixes+ :: ( Monad m, ModifyLocation p s )+ => Int+ -> SP.Stream (SP.Of (PIS i p s)) m r+ -> SP.Stream (SP.Of (PIS i p s)) m r+{-# Inlinable attachPrefixes #-}+attachPrefixes k = SP.map (\(Just w) -> w) . SP.drop 1 . SP.scan go Nothing id+ where+ go Nothing = Just+ go (Just p) = Just . set pisPrefix (Just . locTakeEnd k $ view pisInfix p)++++-- | For each element, attach the suffix as well.+--+-- @1 2 3 4@ -> @12 23 34 40@++attachSuffixes+ :: ( Monad m, ModifyLocation p s )+ => Int+ -> SP.Stream (SP.Of (PIS i p s)) m r+ -> SP.Stream (SP.Of (PIS i p s)) m r+{-# Inlinable attachSuffixes #-}+attachSuffixes k = loop Nothing+ where+ loop Nothing = \case+ SI.Return r -> SI.Return r+ SI.Effect m -> SI.Effect $ fmap (loop Nothing) m+ SI.Step (a SP.:> rest) -> loop (Just a) rest+ loop (Just p) = \case+ SI.Return r -> SI.Step (p SP.:> SI.Return r)+ SI.Effect m -> SI.Effect $ fmap (loop (Just p)) m+ SI.Step (a SP.:> rest) ->+ let p' = p & set pisSuffix (Just . locTake k $ view pisInfix a)+ in SI.Step (p' SP.:> loop (Just a) rest)+
+ Biobase/Types/Names.hs view
@@ -0,0 +1,143 @@++-- | Names for biological things.+--+-- Species names are internalized and represented as an @Int@. This allows+-- using them in structures like an @IntMap@.+--+-- For other names, we newtype-wrap normal text internalization.+--++module Biobase.Types.Names where++import Control.Applicative+import Control.DeepSeq (NFData(..))+import Data.Aeson as A+import Data.Binary as DB+import Data.Hashable+import Data.Interned+import Data.Interned.Text+import Data.Serialize as DS+import Data.Serialize.Text+import Data.String as IS+import Data.String.Conversions (ConvertibleStrings(..), cs)+import Data.String.Conversions.Monomorphic (toST, fromST)+import Data.Text.Binary+import Data.Text (Text, pack, unpack)+import Data.Vector.Unboxed.Deriving+import GHC.Generics++import Biobase.Types.Names.Internal++++-- * Int-internalized species names.++-- | A species name. Represented with an @Int@, but behaves like a @Text@.++newtype SpeciesName = SpeciesName { getSpeciesNameRep :: Int }+ deriving (Eq,Generic)++derivingUnbox "SpeciesName"+ [t| SpeciesName -> Int |]+ [| getSpeciesNameRep |]+ [| SpeciesName |]++instance Ord SpeciesName where+ SpeciesName l `compare` SpeciesName r = speciesNameBimapLookupInt l `compare` speciesNameBimapLookupInt r+ {-# Inline compare #-}++-- | Smart constructor that performs the correct internalization.++speciesName :: Text -> SpeciesName+speciesName = SpeciesName . speciesNameBimapAdd+{-# Inline speciesName #-}++instance IsString SpeciesName where+ fromString = speciesName . IS.fromString+ {-# Inline fromString #-}++instance Show SpeciesName where+ showsPrec p i r = showsPrec p (unpack $ toST i) r+ {-# Inline showsPrec #-}++instance Read SpeciesName where+ readsPrec p str = [ (speciesName $ IS.fromString s, y) | (s,y) <- readsPrec p str ]+ {-# Inline readsPrec #-}++instance Hashable SpeciesName++instance ConvertibleStrings Text SpeciesName where+ convertString = speciesName++instance ConvertibleStrings SpeciesName Text where+ convertString = speciesNameBimapLookupInt . getSpeciesNameRep++instance NFData SpeciesName++instance Binary SpeciesName where+ put = DB.put . toST+ get = fromST <$> DB.get+ {-# Inline put #-}+ {-# Inline get #-}++instance Serialize SpeciesName where+ put = DS.put . toST+ get = fromST <$> DS.get+ {-# Inline put #-}+ {-# Inline get #-}++instance FromJSON SpeciesName where+ parseJSON s = fromST <$> parseJSON s+ {-# Inline parseJSON #-}++instance ToJSON SpeciesName where+ toJSON = toJSON . toST+ {-# Inline toJSON #-}++++-- * Internalize taxonomic rank names++-- | The taxonomic rank. This encodes the name for a given rank.++newtype TaxonomicRank = TaxonomicRank { getTaxonomicRank :: InternedText }+ deriving (IsString,Eq,Ord,Show,Generic)++instance NFData TaxonomicRank where+ rnf (TaxonomicRank it) = rnf (internedTextId it)+ {-# Inline rnf #-}++instance ConvertibleStrings Text TaxonomicRank where+ convertString = TaxonomicRank . intern++instance ConvertibleStrings TaxonomicRank Text where+ convertString = unintern . getTaxonomicRank++instance Hashable TaxonomicRank where+ hashWithSalt s (TaxonomicRank it) = hashWithSalt s (internedTextId it)+ {-# Inline hashWithSalt #-}++instance Read TaxonomicRank where+ readsPrec p str = [ (IS.fromString s, y) | (s,y) <- readsPrec p str ]+ {-# Inline readsPrec #-}++instance Binary TaxonomicRank where+ put = DB.put . toST+ get = fromST <$> DB.get+ {-# Inline put #-}+ {-# Inline get #-}++instance Serialize TaxonomicRank where+ put = DS.put . toST+ get = fromST <$> DS.get+ {-# Inline put #-}+ {-# Inline get #-}++instance FromJSON TaxonomicRank where+ parseJSON s = fromST <$> parseJSON s+ {-# Inline parseJSON #-}++instance ToJSON TaxonomicRank where+ toJSON = toJSON . toST+ {-# Inline toJSON #-}+
+ Biobase/Types/Names/Internal.hs view
@@ -0,0 +1,36 @@++module Biobase.Types.Names.Internal where++import Data.IORef (newIORef,IORef,readIORef,atomicWriteIORef,atomicModifyIORef')+import Data.Text (Text)+import System.IO.Unsafe (unsafePerformIO,unsafeDupablePerformIO)++import Data.Bijection.HashMap+import Data.Bijection.Vector++++speciesNameBimap :: IORef (Bimap (HashMap Text Int) (Vector Text))+speciesNameBimap = unsafePerformIO $ newIORef empty+{-# NoInline speciesNameBimap #-}++-- | Add @Text@ and return @Int@ key. Will return key for+-- existing string and thereby serves for lookup in left-to-right+-- direction.++speciesNameBimapAdd :: Text -> Int+speciesNameBimapAdd k = unsafeDupablePerformIO $ atomicModifyIORef' speciesNameBimap $ \m ->+ case lookupL m k of Just i -> (m,i)+ Nothing -> let s = size m+ in (insert m (k,s) , s)+{-# Inline speciesNameBimapAdd #-}++-- | Lookup the @InternedMultiChar@ based on an @Int@ key. Unsafe totality+-- assumption.++speciesNameBimapLookupInt :: Int -> Text+speciesNameBimapLookupInt r = seq r . unsafeDupablePerformIO $ atomicModifyIORef' speciesNameBimap $ \m ->+ case lookupR m r of Just l -> (m,l)+ Nothing -> error "speciesNameBimapLookupInt: totality assumption invalidated"+{-# Inline speciesNameBimapLookupInt #-}+
− Biobase/Types/Partition.hs
@@ -1,84 +0,0 @@--{-# LANGUAGE ForeignFunctionInterface #-}-{-# LANGUAGE StandaloneDeriving #-}-{-# LANGUAGE MultiParamTypeClasses #-}-{-# LANGUAGE GeneralizedNewtypeDeriving #-}--module Biobase.Types.Partition where--import qualified Data.Vector.Unboxed as VU-import qualified Data.Vector.Generic as VG-import qualified Data.Vector.Generic.Mutable as VGM-import Data.Primitive.Types--import Biobase.Types.Ring------ | Some default instances. Left out the Num one, so that you have to--- explicitly instanciate if you want to go around the Ring structure.--newtype Partition = Partition {unPartition' :: Double}- deriving (Show, Read, Eq, Ord)---- |--mkPartition :: Double -> Partition-mkPartition x- | x < 0 = error $ "mkPartition: prob <0: " ++ show x- | x > 1 = error $ "mkPartition: prob >1: " ++ show x- | otherwise = Partition $ log x--unPartition :: Partition -> Double-unPartition (Partition x) = exp x----- | Ring operations over Partition values.--instance Ring Partition where- (Partition a) .+. (Partition b) = Partition $ logSum a b- {-# INLINE (.+.) #-}- (Partition a) .*. (Partition b) = Partition $ a + b- {-# INLINE (.*.) #-}- (Partition a) .^. k = Partition $ a * fromIntegral k- {-# INLINE (.^.) #-}- (Partition a) .^^. k = error ".^^. not defined for Partition" -- Partition $ a ^^ k- {-# INLINE (.^^.) #-}- neg (Partition a) = error $ "negate partition? " ++ show a -- Partition $ negate a- {-# INLINE neg #-}- one = Partition 1- {-# INLINE one #-}- zero = Partition 0- {-# INLINE zero #-}- isZero (Partition a) = a == 0 -- TODO use some epsilon?- {-# INLINE isZero #-}--logSum :: Double -> Double -> Double-logSum a b- | a>b = f a b- | otherwise = f b a- where- f x y = x + log1p (exp $ y - x)- {-# INLINE f #-}-{-# INLINE logSum #-}------ * Vector (and Prim) instances.--deriving instance VGM.MVector VU.MVector Partition-deriving instance VG.Vector VU.Vector Partition-deriving instance VU.Unbox Partition-deriving instance Prim Partition------ * math.h function for log/exp on pm1 are /much/ more efficient (what is--- haskell doing?)--foreign import ccall unsafe "math.h log1p"- log1p :: Double -> Double--foreign import ccall unsafe "math.h expm1"- expm1 :: Double -> Double-
+ Biobase/Types/Position.hs view
@@ -0,0 +1,163 @@++-- | Annotate the genomic @position@ of features or elements. A @position@ has strand information,+-- and different ways to encode where a feature is located. The @position@ points to the first+-- element (e.g. nucleotide).+--+-- Together with the 'Biobase.Types.Location' module, it becomes possible to annotate substrings.++module Biobase.Types.Position where++import Control.DeepSeq+import Control.Lens hiding (Index, index)+import Data.Data+import GHC.Generics (Generic)+import GHC.TypeNats+import Prelude hiding (length)+import Text.Printf++import Biobase.Types.Index+import Biobase.Types.Strand+import Data.Info++{-++-- | Location information.++data Location = Location+ { _lStrand :: !Strand+ -- ^ On which strand are we+ , _lStart :: !(Index 0)+ -- ^ Start, 0-based+ , _lLength :: !Int+ -- ^ number of characters in this location+ , _lTotalLength :: !Int+ -- ^ the total length of the "contig" (or whatever) this location is positioned in.+ } deriving (Eq,Ord,Read,Show,Generic)+makeLenses ''Location+makePrisms ''Location++instance NFData Location++instance Semigroup Location where+ x <> y = let f z = z { _lLength = _lLength x + _lLength y }+ in case x^.lStrand of+ MinusStrand -> f y+ _otherStrand -> f x+ {-# Inline (<>) #-}++--instance Reversing Location where+-- {-# Inline reversing #-}+-- reversing = undefined+++-- | An isomorphism between locations, and triples of @Strand,Start,End@, where+-- end is inclusive. For @length==0@ locations, this will mean @start<end@ on+-- the plus strand.+--+-- This should hold for all @k@, in @Index k@.++startEndInclusive :: (KnownNat k) => Iso' Location (Strand, (Index k, Index k), Int)+{-# Inline startEndInclusive #-}+startEndInclusive = iso l2r r2l+ where l2r z = let s = z^.lStrand; f = z^.lStart; l = z^.lLength+ in (s, (reIndex f, reIndex $ f +. l -. 1), z^.lTotalLength)+ r2l (s,(f,t),ttl) = Location s (reIndex f) (delta f t + 1) ttl++-}++++-- | During streaming construction, it is possible that we know a feature is on the @-@ strand, but+-- the length of the contig is not known yet. In that case, 'FwdPosition' allows expressing the hit+-- in the coordinate system of the plus strand. Tools like blast do something similar, and express+-- locations on the minus as @y-x@ with @y>x@.+--+-- @+-- 0123456789+-- >-->+-- <--<+-- 9876543210+-- @+--+-- ++data FwdPosition+ -- | "Plus"-based location.+ = FwdPosition+ { _fwdStrand :: !Strand+ -- ^ Strand we are on+ , _fwdStart :: !(Index 0)+ -- ^ Start of the hit on the plus strand+ }+ deriving (Eq,Ord,Read,Show,Data,Typeable,Generic)+makeLenses ''FwdPosition+makePrisms ''FwdPosition++instance NFData FwdPosition++instance Info FwdPosition where+ info (FwdPosition s x) = printf "%s %d" (show s) (toInt0 x)++-- | Reversing a reversible location means moving the start to the end.++instance Reversing FwdPosition where+ {-# Inline reversing #-}+ reversing x = case x^.fwdStrand of+ PlusStrand -> set fwdStrand MinusStrand $ x+ MinusStrand -> set fwdStrand PlusStrand $ x+ UnknownStrand -> x++{-+++-- | Combining two FwdLocations yields the sum of their lengths. This assumes+-- that @x@ and @y@ are next to each other, or that it is ok if the @y@+-- @fwdStart@ information may be lost.+--+-- TODO provide associativity test in @properties@.++instance Semigroup FwdLocation where+ x <> y = over fwdLength (+ view fwdLength y) x+ {-# Inline (<>) #-}++instance ModifyLocation FwdLocation where+ locMoveLeftEnd k = over fwdStart (+. k) . over fwdLength (subtract k)+ locMoveRightEnd k = over fwdLength (+k)++-- | Given a location, take at most @k@ elements, and return a location after+-- this change.++fwdLocationTake :: Int -> FwdLocation -> FwdLocation+{-# Inline fwdLocationTake #-}+fwdLocationTake k' x =+ let l = x^.fwdLength+ k = max 0 $ min k' l -- deal with at most the length of the location+ in case x^.fwdStrand of+ MinusStrand -> set fwdLength k $ over fwdStart (+. (l-k)) x+ _otherStrand -> set fwdLength k $ x++-- | Given a location, drop at most @k@ elements, and return a location after+-- this change.+--+-- Note that @fwdLocationDrop 4 (FwdLocation PlusStrand 0 4) == FwdLocation 4 0@++fwdLocationDrop :: Int -> FwdLocation -> FwdLocation+{-# Inline fwdLocationDrop #-}+fwdLocationDrop k' x =+ let l = x^.fwdLength+ k = max 0 $ min k' l+ in case x^.fwdStrand of+ MinusStrand -> set fwdLength (l-k) $ x+ _otherStrand -> set fwdLength (l-k) $ over fwdStart (+. min k l) x++-- -- An isomorphism between a 'Location' and the pair @('FwdLocation',Int)@+-- -- exists.+-- +-- locationPartial :: Iso' Location (FwdLocation,Int)+-- {-# Inline locationPartial #-}+-- locationPartial = iso l2r r2l where+-- l2r l = undefined+-- r2l (p,z) = undefined++-}+
+ Biobase/Types/ReadingFrame.hs view
@@ -0,0 +1,54 @@++-- | Stranded reading frames.++module Biobase.Types.ReadingFrame where++import Control.Lens hiding (Index)+import GHC.Generics hiding (from)++import Biobase.Types.Index (Index, toInt0)+import Biobase.Types.Strand++++-- | The Reading frame. Sequence indexing starts at position 1, which starts+-- reading frame 1. Reading frame 2 and 3 start at position 2 and 3+-- respectively.++newtype ReadingFrame = ReadingFrame { getReadingFrame ∷ Int }+ deriving (Eq,Ord,Generic,Show)+makeWrapped ''ReadingFrame++-- | Convert between @+1 ... +3@ and @ReadingFrame@.++rf ∷ Prism' Int ReadingFrame+{-# Inline rf #-}+rf = prism' getReadingFrame $ \k → let ak = abs k in+ if (ak <= 3 && ak >= 1) then Just (ReadingFrame k) else Nothing++-- | A lens for the strand++strandRF ∷ Lens' ReadingFrame Strand+{-# Inline strandRF #-}+strandRF = lens (\(ReadingFrame k) → if k < 0 then MinusStrand else PlusStrand)+ (\(ReadingFrame k) s → ReadingFrame $ if s == PlusStrand then abs k else (negate $ abs k))++-- |+--+-- @pred@ and @succ@ are correct, if the input is a legal 'ReadingFrame'.++instance Enum ReadingFrame where+ {-# Inline toEnum #-}+ toEnum k = case k^?rf of Just rf → rf ; Nothing → error $ show k ++ " is not a legal reading frame"+ {-# Inline fromEnum #-}+ fromEnum = getReadingFrame++-- |+--+-- TODO should this be a type class, since we might reasonably want to+-- construct from a number of possible indices?++fromIndex ∷ Index 1 → ReadingFrame+{-# Inline fromIndex #-}+fromIndex i = ReadingFrame $ (toInt0 i `mod` 3) + 1+
− Biobase/Types/Ring.hs
@@ -1,22 +0,0 @@---- | Algebraic ring structure. Very similar to others found throughout hackage.------ TODO maybe use on of the already-written packages?--module Biobase.Types.Ring where------ | Define the basic operations on a ring.--class (Eq a, Ord a) => Ring a where- (.+.), (.*.) :: a -> a -> a- (.^.) :: a -> Int -> a- (.^^.) :: a -> Double -> a- neg :: a -> a- one, zero :: a- isZero :: a -> Bool -- ^ ==zero does not work well for min-plus- infixl 6 .+.- infixl 7 .*.- infixr 8 .^.- infixr 8 .^^.
− Biobase/Types/Score.hs
@@ -1,48 +0,0 @@--{-# LANGUAGE StandaloneDeriving #-}-{-# LANGUAGE MultiParamTypeClasses #-}-{-# LANGUAGE GeneralizedNewtypeDeriving #-}--module Biobase.Types.Score where--import qualified Data.Vector.Unboxed as VU-import qualified Data.Vector.Generic as VG-import qualified Data.Vector.Generic.Mutable as VGM-import Data.Primitive.Types--import Biobase.Types.Ring------ | Some default instances. Left out the Num one, so that you have to--- explicitly instanciate if you want to go around the Ring structure.--newtype Score = Score {unScore :: Int}- deriving (Show, Read, Eq, Ord)------ | Ring operations over Score values.--instance Ring Score where- (Score a) .+. (Score b) = Score $ a `min` b- {-# INLINE (.+.) #-}- (Score a) .*. (Score b) = Score $ a + b- {-# INLINE (.*.) #-}- neg (Score a) = Score $ negate a- {-# INLINE neg #-}- one = Score 0- {-# INLINE one #-}- zero = Score 10000000- {-# INLINE zero #-}- isZero (Score a) = a >= 1000000- {-# INLINE isZero #-}------ * Vector instances.--deriving instance VGM.MVector VU.MVector Score-deriving instance VG.Vector VU.Vector Score-deriving instance VU.Unbox Score-deriving instance Prim Score
+ Biobase/Types/Shape.hs view
@@ -0,0 +1,202 @@++-- | Shape abstractions of structures.+--+-- Shapes do not preserve sizes of structures (say unpaired regions or stem+-- length). As such, distance measures provided here are to be used carefully!+--+-- TODO consider how to handle the different shape levels. One option would be+-- to phantom-type everything.++module Biobase.Types.Shape where++import Control.DeepSeq+import Control.Lens+import Control.Monad.Error.Class+import Control.Monad (foldM,unless)+import Data.ByteString (ByteString)+import Data.Data+import Data.List (foldl1')+import Data.Monoid ((<>))+import Data.Set (Set)+import GHC.Generics (Generic)+import qualified Data.ByteString.Char8 as BS8+import qualified Data.List as L+import qualified Data.Set as Set++import Data.Forest.StructuredPaired++import qualified Biobase.Types.Structure as TS++++-- | Shape levels are hardcoded according to their specification.+--+-- TODO Allow compile-time check on accepted shape levels?++data ShapeLevel+ = SL1+ | SL2+ | SL3+ | SL4+ | SL5+ deriving (Eq,Ord,Show,Read,Data,Typeable,Generic)++instance NFData ShapeLevel++++-- | The type of RNA shapes. Keeps the type ++data RNAshape+ = RNAshape+ { _rnashapelevel ∷ !ShapeLevel+ -- ^ The type of shape encoded here.+ , _rnashape ∷ !ByteString+ -- ^ The actual shape as a string.+ }+ deriving (Eq,Ord,Show,Read,Data,Typeable,Generic)+makeLenses ''RNAshape++instance NFData RNAshape++++-- | Given a compactified 'SPForest', creates a shape forest of the given level.+--+--+--+-- TODO needs newtyping++shapeForest+ ∷ ShapeLevel+ → SPForest ByteString ByteString+ → SPForest Char Char+shapeForest = preStem+ where+ -- | In @preStem@, we aim to close in on the next stem. @SPE@ means that we+ -- reached an end in a stem.+ preStem s SPE = SPE+ -- | The start of a tree structure. The forest is compact, which means that+ -- the element in @xs@ is, by definition, not a continuation of a stack.+ preStem s (SPT _ xs _) = SPT '[' (inStem s xs) ']'+ -- |+ preStem s spr@(SPR rs) = inStem s spr -- = error $ "preStem/SPR " ++ show rs+ -- |+ preStem s (SPJ xs)+ | [x] ← xs = preStem s x+ -- left bulge+ | [l@SPR{},x@SPT{}] ← xs = if s <= SL2 then (SPJ [SPR '_', preStem s x]) else preStem s x+ -- right bulge+ | [x@SPT{},r@SPR{}] ← xs = if s <= SL2 then (SPJ [preStem s x, SPR '_']) else preStem s x+ | otherwise = SPJ $ map (preStem s) xs -- error $ "preStem/SPJ " ++ show xs+ --+ -- | After a stem, there could be an @SPE@ element.+ inStem s SPE = SPE+ -- | This case happens when eradicating unstructured regions with high+ -- abstraction levels.+ inStem s (SPT _ xs _) = inStem s xs+ inStem s (SPR rs)+ | s == SL1 = SPR '_' -- = error $ "inStem / SPR " ++ show rs+ | otherwise = SPE+ inStem s (SPJ xs)+ | [x] ← xs = error "x"+ -- left bulge+ | [l@SPR{},x] ← xs = if s <= SL3 then preStem s (SPJ xs) else inStem s x+ -- right bulge+ | [x,r@SPR{}] ← xs = if s <= SL3 then preStem s (SPJ xs) else inStem s x+ -- interior loop+ | [l@SPR{},x,r@SPR{}] ← xs = if s == SL5 then inStem s x else preStem s (SPJ xs)+-- | s == SL1 = error $ "inStem / SPJ " ++ show xs+-- | s == SL2 = error $ "inStem / SPJ " ++ show xs+ -- multibranched loop+ | otherwise = SPJ $ map (preStem s) xs++rnass2shape lvl s = shapeForestshape lvl . shapeForest lvl . TS.compactifySPForest+ . either (\e → error $ show (e,s)) id . TS.rnassSPForest $ s++-- | turn into unit test. also reverse of the input should give reverse shape!+-- this then gives a quickcheck test, reversing the input should reverse the shape+--+-- TODO requires generating secondary structures via @Arbitrary@.++test lvl = shapeForestshape lvl . shapeForest lvl $ TS.compactifySPForest $ either error id $ TS.rnassSPForest $ TS.RNAss "(((((...(((..(((...))))))...(((..((.....))..)))))))).."++{-+shapeForest SL5 = go+ where+ go SPE = SPE+ go (SPT _ xs _)+ | SPE ← xs, SPR{} ← xs, [] ← ts = SPT '[' SPE ']'+ | [t] ← ts = go t+ | otherwise = SPT '[' (SPJ $ map go ts) ']'+ where (SPJ ys) = xs+ ts = [ t | t@SPT{} ← ys ]+ -- should only happen on a single unfolded structure+ go (SPR _) = SPR '_'+ go (SPJ xs)+ | [] ← ts = SPR '_'+ | [t] ← ts = go t+ | otherwise = SPJ $ map go ts+ where ts = [ t | t@SPT{} ← xs ]+ go xs = error $ show xs ++ " should no be reached"+-}++-- | ++shapeForestshape+ ∷ ShapeLevel+ → SPForest Char Char+ → RNAshape+shapeForestshape lvl = RNAshape lvl . go+ where+ go SPE = ""+ go (SPT l x r) = BS8.singleton l <> go x <> BS8.singleton r+ go (SPJ xs ) = mconcat $ map go xs+ go (SPR x ) = BS8.singleton x -- error "should not be reached" -- BS8.singleton x++generateShape ∷ ShapeLevel → TS.RNAss → RNAshape+generateShape = undefined+++-- * Distance measures on the shape string itself.++-- | Wrapper for string-positional shapes. Intentionally chosen long name.++data RNAshapepset = RNAshapepset { _rnashapepsetlevel ∷ ShapeLevel, _rnashapepset ∷ Set (Int,Int) }+ deriving (Read,Show,Eq,Ord,Generic)+makeLenses ''RNAshapepset++instance NFData RNAshapepset++-- | Transform an 'RNAss' into a set of base pairs @(i,j)@. The pairs are+-- 0-based.++rnashapePairSet+ ∷ (MonadError String m)+ ⇒ RNAshape+ → m RNAshapepset+rnashapePairSet (RNAshape lvl s2) = do+ let go (set,ks ) (i,'[') = return (set,i:ks)+ go (set,i:is) (j,']') = return (Set.insert (i,j) set, is)+ go (set,[] ) (j,']') = throwError $ "unequal brackets in \"" ++ BS8.unpack s2 ++ "\" at position: " ++ show j+ go (set,ks ) (_,'_') = return (set,ks)+ (set,ss) ← foldM go (Set.empty,[]) . L.zip [0..] $ BS8.unpack s2+ unless (null ss) $ throwError $ "unequal brackets in \"" ++ BS8.unpack s2 ++ "\" with opening bracket(s): " ++ show ss+ return $ RNAshapepset lvl set+{-# Inlinable rnashapePairSet #-}++-- | RNA pair set, but a transformation error calls @error@.++rnassPairSet' ∷ RNAshape → RNAshapepset+rnassPairSet' = either error id . rnashapePairSet++-- | Calculates the number of different base pairs betwwen two structures.+--+-- TODO error out on different shape levels++shapePairDist ∷ RNAshapepset → RNAshapepset → Int+shapePairDist (RNAshapepset lvl1 p1) (RNAshapepset lvl2 p2) = Set.size z1 + Set.size z2+ where i = Set.intersection p1 p2+ z1 = p1 `Set.difference` i+ z2 = p2 `Set.difference` i+
+ Biobase/Types/Strand.hs view
@@ -0,0 +1,147 @@++-- | Strand information. A newtyped version, complete with serialization,+-- pattern synonyms, being a @PrimitiveArray@ index type, etc. The strand+-- information includes @+@, @-@, as well as the (GFF3) @.@ not stranded, and+-- @?@ for unknown strand information.+--+-- TODO will be expanded to encode biological sense information more clearly:+-- <http://en.wikipedia.org/wiki/Sense_%28molecular_biology%29>.++module Biobase.Types.Strand where++import Control.DeepSeq+import Control.Lens hiding (Index)+import Control.Monad (guard)+import Data.Aeson+import Data.Binary+import Data.Data (Data)+import Data.Hashable (Hashable)+import Data.Serialize (Serialize)+import Data.Typeable (Typeable)+import Data.Vector.Fusion.Stream.Monadic (Step(..), flatten)+import Data.Vector.Unboxed.Deriving+import GHC.Generics+import Test.QuickCheck+import Text.Printf++import Data.PrimitiveArray.Index.Class++++-- | Encode strand information. 'PlusStrand' is defined as the strand encoded+-- in, say, the FASTA file. 'MinusStrand' hence is the reverse complement.++newtype Strand = Strand { getStrand :: Int }+ deriving (Eq,Ord,Generic,Data,Typeable)++instance Show Strand where+ show PlusStrand = "PlusStrand"+ show MinusStrand = "MinusStrand"+ show NotStranded = "NotStranded"+ show UnknownStrand = "UnknownStrand"++instance Read Strand where+ readsPrec _ xs = do+ (pm,s) <- lex xs+ case pm of+ "PlusStrand" -> return (PlusStrand, s)+ "MinusStrand" -> return (MinusStrand, s)+ "NotStranded" -> return (NotStranded, s)+ "UnknownStrand" -> return (UnknownStrand, s)+ [x] | x `elem` ("+Pp" :: String) -> return (PlusStrand,s)+ | x `elem` ("-Mm" :: String) -> return (MinusStrand,s)+ | x `elem` ("." :: String) -> return (NotStranded,s)+ | x `elem` ("?" :: String) -> return (UnknownStrand,s)+ _ -> []++instance Bounded Strand where+ minBound = PlusStrand+ maxBound = UnknownStrand++instance Enum Strand where+ succ (Strand k)+ | k < 0 = error "succ undefined strand"+ | k == 3 = error "succ UnknownStrand"+ | k > 3 = error "succ undefined strand"+ | otherwise = Strand (k+1)+ pred (Strand k)+ | k < 0 = error "pred undefined strand"+ | k == 0 = error "pred UnknownStrand"+ | k > 3 = error "pred undefined strand"+ | otherwise = Strand (k-1)+ toEnum i | i>=0 && i<=3 = Strand i+ toEnum i = error $ "toEnum (Strand)" ++ show i+ fromEnum = getStrand++instance Reversing Strand where+ reversing PlusStrand = MinusStrand+ reversing MinusStrand = PlusStrand+ reversing x = x++pattern PlusStrand = Strand 0+pattern MinusStrand = Strand 1+pattern NotStranded = Strand 2+pattern UnknownStrand = Strand 3++-- TODO Sense and Antisense are somewhat different++--pattern Sense = P+--pattern AntiSense = M++instance Binary Strand+instance Serialize Strand+instance ToJSON Strand+instance FromJSON Strand+instance Hashable Strand+instance NFData Strand++derivingUnbox "Strand"+ [t| Strand -> Int |] [| getStrand |] [| Strand |]++instance Index Strand where+ newtype (LimitType Strand) = LtStrand Strand+ linearIndex _ (Strand z) = z+ {-# INLINE linearIndex #-}+ size (LtStrand (Strand h)) = h + 1+ {-# INLINE size #-}+ inBounds (LtStrand (Strand h)) (Strand x) = 0<=x && x<=h+ {-# INLINE inBounds #-}+ zeroBound = Strand 0+ {-# Inline zeroBound #-}+ zeroBound' = LtStrand zeroBound+ {-# Inline zeroBound' #-}+ totalSize (LtStrand (Strand k)) = [ fromIntegral (fromEnum k + 1) ]+ {-# Inline totalSize #-}+ fromLinearIndex _ = Strand+ {-# Inline [0] fromLinearIndex #-}+ showBound (LtStrand k) = ["LtStrand " ++ show k]+ showIndex (Strand k) = ["Strand " ++ show k]++instance IndexStream z => IndexStream (z:.Strand) where+ streamUp (ls:..LtStrand (Strand lf)) (hs:..LtStrand (Strand ht)) = flatten mk step $ streamUp ls hs+ where mk z = return (z,lf)+ step (z,k)+ | k > ht = return $ Done+ | otherwise = return $ Yield (z:.Strand k) (z,k+1)+ {-# Inline [0] mk #-}+ {-# Inline [0] step #-}+ {-# Inline streamUp #-}+ streamDown (ls:..LtStrand (Strand lf)) (hs:..LtStrand (Strand ht)) = flatten mk step $ streamDown ls hs+ where mk z = return (z,ht)+ step (z,k)+ | k < lf = return $ Done+ | otherwise = return $ Yield (z:.Strand k) (z,k-1)+ {-# Inline [0] mk #-}+ {-# Inline [0] step #-}+ {-# Inline streamDown #-}++-- instance IndexStream Strand++instance Arbitrary Strand where+ arbitrary = do+ b <- choose (0,3)+ return $ Strand b+ shrink (Strand j)+ | 0<j = [Strand $ j-1]+ | otherwise = []+
+ Biobase/Types/Structure.hs view
@@ -0,0 +1,225 @@++-- | Wrappers for structural data. Encoded as bytestrings. This differs from+-- @BiobaseXNA@, where specialized encodings are used. These structures are+-- supposedly "short", they need to fit into a strict bytestring.+--+-- TODO Consider where to move each type. There are merge possibilities between+-- BiobaseXNA and BiobaseTypes.+--+-- TODO QuickCheck @Arbitrary@ for @RNAss@.++module Biobase.Types.Structure where++import Control.Applicative+import Control.DeepSeq+import Control.Lens+import Control.Monad.Error.Class+import Control.Monad (foldM,unless)+import Data.Attoparsec.ByteString.Char8+import Data.Attoparsec.Combinator+import Data.Bifunctor (second)+import Data.ByteString (ByteString)+import Data.Data+import Data.List (foldl1',foldl')+import Data.Monoid ((<>))+import Data.Set (Set)+import GHC.Generics (Generic)+import qualified Data.ByteString.Char8 as BS8+import qualified Data.List as L+import qualified Data.Set as S+import qualified Data.Set as Set+import qualified Data.Vector.Unboxed as VU+import qualified Test.QuickCheck as Q++import Data.Forest.StructuredPaired++++-- | Secondary structure using @()@ for paired elements, and @.@ for unpaired+-- ones. It is assumed that the @()@ match up. These structures from a Monoid.++newtype RNAss = RNAss { _rnass ∷ ByteString }+ deriving (Eq,Ord,Show,Read,Data,Typeable,Generic,Semigroup,Monoid)+makeLenses ''RNAss++instance NFData RNAss++-- | Ensemble structure encoding. *Very* different type ctor name chosen! The+-- structure of this string makes verification much more complicated.+--+-- TODO describe encoding used by RNAfold for the ensemble string.++newtype RNAensembleStructure = RNAes { _rnaes ∷ ByteString }+ deriving (Eq,Ord,Show,Read,Data,Typeable,Generic)+makeLenses ''RNAensembleStructure++instance NFData RNAensembleStructure++-- | Cofolded structure.++data RNAds = RNAds+ { _rnadsL ∷ !ByteString+ , _rnadsR ∷ !ByteString+ }+ deriving (Eq,Ord,Show,Read,Data,Typeable,Generic)+makeLenses ''RNAds++instance NFData RNAds++-- | A Prism that turns ByteStrings with a single @&@ into @RNAds@.++rnads ∷ Prism' ByteString RNAds+rnads = prism (\(RNAds l r) → BS8.concat [l, "&", r])+ (\s → case BS8.split '&' s of [l,r] → Right (RNAds l r) ; _ → Left s)+{-# Inline rnads #-}++-- | Isomorphism from @RNAds@ to @(RNAss,RNAss)@. The @RNAss@ are only+-- legal if taken both: @rnassFromDimer . both@.++rnads2rnassPair ∷ Iso' RNAds (RNAss, RNAss)+rnads2rnassPair = iso (\(RNAds l r) → (RNAss l, RNAss r)) (\(RNAss l, RNAss r) → RNAds l r)+{-# Inline rnads2rnassPair #-}++-- | Try to create a dimeric structure.++mkRNAds ∷ (Monad m, MonadError RNAStructureError m) ⇒ ByteString → m RNAds+mkRNAds q = BS8.split '&' q & \case+ [l,r] → do+ -- TODO can still fail with unmatched brackets.+ return $ RNAds+ { _rnadsL = l+ , _rnadsR = r+ }+ _ → throwError $ RNAStructureError "mkRNAds: not a dimer" q+{-# Inline mkRNAds #-}++-- | Capture what might be wrong with the RNAss.++data RNAStructureError = RNAStructureError+ { _rnaStructureError ∷ String+ , _rnaOffender ∷ ByteString+ }+ deriving (Show,Generic)++instance NFData RNAStructureError++-- | Verifies that the given RNAss is properly formatted. Otherwise, error out.+--+-- TODO Implement! Check with BiobaseXNA and the stack effort in there. This+-- might influence if the verification goes into BiobaseXNA and happens via an+-- @Iso'@.++verifyRNAss ∷ (Monad m, MonadError RNAStructureError m) ⇒ RNAss → m RNAss+verifyRNAss ss = do+ return ss++-- | The set of nucleotide pairs, together with the sequence length.++data RNApset = RNApset+ { _rnapset ∷ !(Set (Int,Int))+ -- ^ the set of nucleotide pairs.+ , _rnapsetSLen ∷ !Int+ -- ^ length of the underlying nucleotide sequence.+ }+ deriving (Read,Show,Eq,Ord,Generic)+makeLenses ''RNApset++instance NFData RNApset++-- | Transform an 'RNAss' into a set of base pairs @(i,j)@. The pairs are+-- 0-based.++rnassPairSet+ ∷ (MonadError String m)+ ⇒ RNAss+ → m RNApset+rnassPairSet (RNAss s2) = do+ let go (set,ks ) (i,'(') = return (set,i:ks)+ go (set,i:is) (j,')') = return (Set.insert (i,j) set, is)+ go (set,[] ) (j,')') = throwError $ "unequal brackets in \"" ++ BS8.unpack s2 ++ "\" at position: " ++ show j+ go (set,ks ) (_,'.') = return (set,ks)+ (set,ss) ← foldM go (Set.empty,[]) . L.zip [0..] $ BS8.unpack s2+ unless (null ss) $ throwError $ "unequal brackets in \"" ++ BS8.unpack s2 ++ "\" with opening bracket(s): " ++ show ss+ return $ RNApset set (BS8.length s2)+{-# Inlinable rnassPairSet #-}++-- | Genereate a simple structured/paired forest from a secondary structure string.++rnassSPForest+ ∷ (MonadError String m)+ ⇒ RNAss+ → m (SPForest ByteString Char)+rnassSPForest (RNAss s2) = either throwError return $ parseOnly (manyElems <* endOfInput) s2+ where+ tree = SPT <$> char '(' <*> someElems <*> char ')' <?> "SPT"+ unpaired = SPR <$> takeWhile1 (=='.') <?> "SPR"+ someElems = SPJ <$> many1 (tree <|> unpaired) <?> "many1 SPT / SPR"+ manyElems = (\case {[] → SPE; xs → SPJ xs}) <$> many (tree <|> unpaired) <?> "many0 SPT / SPR"+{-# Inlinable rnassSPForest #-}++-- | Compactify such an SPForest. This means that all stems are now represented+-- by a single 'SPT' data constructor.++compactifySPForest+ ∷ SPForest ByteString Char+ → SPForest ByteString ByteString+compactifySPForest = go . second BS8.singleton+ where go SPE = SPE+ go (SPR x) = SPR x+ go (SPJ xs) = SPJ (map go xs)+ go (SPT l (SPJ [x]) r) = go $ SPT l x r+ go (SPT l (SPT l' t r') r) = go $ SPT (l <> l') t (r' <> r)+ go (SPT l t r) = SPT l (go t) r++-- | RNA pair set, but a transformation error calls @error@.++rnassPairSet' ∷ RNAss → RNApset+rnassPairSet' = either error id . rnassPairSet++rnapsetRNAss ∷ RNApset → RNAss+rnapsetRNAss (RNApset ps l) = RNAss $ BS8.pack $ VU.toList xs+ where xs = VU.replicate l '.' VU.// ls VU.// rs+ ls = L.map ((,'(') . fst) $ S.toList ps+ rs = L.map ((,')') . snd) $ S.toList ps++-- | Calculates the number of different base pairs between two structures. This+-- ignores the length of the underlying sequences.++pairDist ∷ RNApset → RNApset → Int+pairDist (RNApset p1 _) (RNApset p2 _) = Set.size z1 + Set.size z2+ where i = Set.intersection p1 p2+ z1 = p1 `Set.difference` i+ z2 = p2 `Set.difference` i++++-- * Arbitrary instances. This only creates legal instances, but does *not*+-- take into account ViennaRNA rules like three unpaired nucleotides in the+-- hairpin.+--+-- TODO @shrink@ is a bit more complicated, but can be done via a set of pairs.++instance Q.Arbitrary RNApset where+ arbitrary = do+ -- Given left and right bounds, create pairs.+ let go ∷ Int → Int → Q.Gen (Set (Int,Int))+ go l r+ | l >= r = return S.empty+ | otherwise = do+ -- right border of stack+ c ∷ Int ← Q.oneof [ Q.choose (l+1,r) -- wide jump+ , Q.choose (l+1, min r $ l+20) -- short jump+ ]+ -- with @1..10@ stack length+ z ∷ Int ← Q.choose (0,5)+ let stack = S.fromList [(l+k,c-k) | k ← [0..z-1], l+k+1 < c-k]+ right ← go (c+1) r+ return $ S.union stack right+ -- generate RNA structures between 0 and 100 nucleotides.+ l ∷ Int ← Q.choose (0,199)+ s ← go 0 l+ return $ RNApset s (l+1)++instance Q.Arbitrary RNAss where+ arbitrary = rnapsetRNAss <$> Q.arbitrary+
+ Biobase/Types/Taxonomy.hs view
@@ -0,0 +1,71 @@++-- | Biological classification of species.++module Biobase.Types.Taxonomy where++import Control.DeepSeq+import Data.Aeson+import Data.Binary+import Data.Hashable (Hashable, hashWithSalt)+import Data.Primitive.Types+import Data.Serialize+import Data.Text (Text)+import Data.Vector.Binary+import Data.Vector.Serialize+import Data.Vector.Unboxed.Deriving+import Data.Vector (Vector)+import GHC.Generics (Generic)++import Biobase.Types.Accession (Accession,Species)+import Biobase.Types.Names (SpeciesName, TaxonomicRank)++++-- | Taxonomic classification. @Enum@ together with a final @Unknown@ is+-- somewhat fishy.+--+-- TODO What should the order be? Kingdom > Species or Kingdom < Species?++data Classification+ = Kingdom+ | Phylum+ | Class+ | Order+ | SubOrder+ | Family+ | Genus+ | Species+ | Unknown+ deriving (Eq,Ord,Read,Show,Enum,Generic)++instance Binary Classification+instance FromJSON Classification+instance Hashable Classification+instance Serialize Classification+instance ToJSON Classification+instance NFData Classification++derivingUnbox "Classification"+ [t| Classification -> Int |] [| fromEnum |] [| toEnum |]++++-- | A somewhat generic representation of a species within a taxonomic+-- context.++data Taxon = Taxon+ { species :: !SpeciesName -- ^ the full, formal name of a species+ , accession :: !(Accession Species) -- ^ the accession for the species (or @""@ if unknown)+ , classification :: !(Vector (TaxonomicRank,Classification)) -- ^ vector with classification information+ }+ deriving (Eq,Read,Show,Generic)++instance Binary Taxon+instance FromJSON Taxon+instance Serialize Taxon+instance ToJSON Taxon+instance NFData Taxon++instance Hashable Taxon where+ hashWithSalt h (Taxon s a _) = hashWithSalt h (s,a)+
BiobaseTypes.cabal view
@@ -1,37 +1,150 @@+cabal-version: 2.2 name: BiobaseTypes-version: 0.0.2.2-author: Christian Hoener zu Siederdissen-maintainer: choener@tbi.univie.ac.at-copyright: Christian Hoener zu Siederdissen, 2010-category: Bioinformatics-synopsis: (deprecated) Ring class, with several instances.-license: GPL-3+version: 0.2.1.0+author: Christian Hoener zu Siederdissen, 2015 - 2021+copyright: Christian Hoener zu Siederdissen, 2015 - 2021+homepage: https://github.com/choener/BiobaseTypes+bug-reports: https://github.com/choener/BiobaseTypes/issues+maintainer: choener@bioinf.uni-leipzig.de+category: Data Structures, Bioinformatics+license: BSD-3-Clause license-file: LICENSE build-type: Simple stability: experimental-cabal-version: >= 1.4.0+tested-with: GHC == 8.8, GHC == 8.10, GHC == 9.0+synopsis: Collection of types for bioinformatics description:- Provides an algebraic ring class and instances for Gibbs free- energy, partition function probabilities, and scores.- Conversion between different entities is provided by a convert- function. All entities are ready for the vector library.+ Types used in a number of bioinformatics libraries. .- - Ignore everything except the Ring itself!+ * linear indices+ .+ * energies+ .+ * biostring wrappers -library- build-depends:- base >=4 && <5,- vector >=0.7 && <0.8,- primitive >=0.3 && <0.4+Extra-Source-Files:+ README.md+ changelog.md +++common deps+ build-depends: base >= 4.7 && < 5.0+ , aeson >= 0.8+ , attoparsec >= 0.13+ , binary >= 0.7+ , bytestring+ , cereal >= 0.4+ , cereal-text >= 0.1+ , cereal-vector >= 0.2+ , containers+ , data-default >= 0.5+ , deepseq >= 1.4+ , hashable >= 1.2+ , intern >= 0.9+ , lens >= 4.0+ , mtl+ , primitive >= 0.5+ , QuickCheck >= 2.7+ , streaming >= 0.1+ , string-conversions >= 0.4+ , text >= 1.0+ , text-binary >= 0.2+ , utf8-string >= 1.0+ , vector >= 0.10+ , vector-binary-instances >= 0.2+ , vector-th-unbox >= 0.2+ --+ , bimaps == 0.1.0.*+ , DPutils == 0.1.1.*+ , ForestStructures == 0.0.1.*+ , PrimitiveArray >= 0.10.1.1 && < 0.10.2+ , SciBaseTypes == 0.1.1.*+ default-language:+ Haskell2010+ default-extensions: BangPatterns+ , DataKinds+ , DeriveDataTypeable+ , DeriveFoldable+ , DeriveGeneric+ , DeriveTraversable+ , DerivingStrategies+ , FlexibleContexts+ , FlexibleInstances+ , GeneralizedNewtypeDeriving+ , KindSignatures+ , LambdaCase+ , MultiParamTypeClasses+ , OverloadedStrings+ , PatternSynonyms+ , PolyKinds+ , RankNTypes+ , RecordWildCards+ , ScopedTypeVariables+ , StandaloneDeriving+ , TemplateHaskell+ , TypeApplications+ , TypeFamilies+ , TypeOperators+ , TupleSections+ , UndecidableInstances+ , UnicodeSyntax+ , ViewPatterns+ ghc-options:+ -O2 -funbox-strict-fields++++library+ import:+ deps exposed-modules:- Biobase.Types.Ring- Biobase.Types.Convert+ Biobase.Types.Accession+ Biobase.Types.BioSequence+ Biobase.Types.Bitscore+ Biobase.Types.Codon Biobase.Types.Energy- Biobase.Types.Partition- Biobase.Types.Score+ Biobase.Types.Evalue+ Biobase.Types.Index+ Biobase.Types.Index.Type+ Biobase.Types.Location+ Biobase.Types.Names+ Biobase.Types.Names.Internal+ Biobase.Types.Position+ Biobase.Types.ReadingFrame+ Biobase.Types.Shape+ Biobase.Types.Strand+ Biobase.Types.Structure+ Biobase.Types.Taxonomy+ DP.Backtraced.BioSequence+ DP.Backtraced.Codon - ghc-options:- -O2+++test-suite properties+ import:+ deps+ type:+ exitcode-stdio-1.0+ main-is:+ properties.hs+-- ghc-options:+-- -threaded -rtsopts -with-rtsopts=-N+ hs-source-dirs:+ tests+ build-depends: base+ , tasty >= 0.11+ , tasty-hunit >= 0.10+ , tasty-quickcheck >= 0.8+ , tasty-th >= 0.1+ --+ , BiobaseTypes++++source-repository head+ type: git+ location: git://github.com/choener/BiobaseTypes+
+ DP/Backtraced/BioSequence.hs view
@@ -0,0 +1,3 @@++module DP.Backtraced.BioSequence where+
+ DP/Backtraced/Codon.hs view
@@ -0,0 +1,46 @@++-- | The Backtraced column structure is for codon-based alignments, including+-- special cases.++module DP.Backtraced.Codon where++import Data.ByteString (ByteString)+import Data.Vector (Vector)+import GHC.Generics (Generic)++import Biobase.Types.Codon++++-- | A single 'Backtraced' column. Since such a column will be part of a+-- @Backtraced (Z:.BtCodon c aa:. ...)@ structure, it is always possible to+-- extend even further, by having more entries.++data BtCodon c aa+ -- | A canonical match. A codon and the translated amino acid need to be set.+ = Match+ { _codon ∷ !(Codon c)+ , _aa ∷ !aa+ }+ -- | A frameshifting match. The vector of frameshifted nucleotides will have+ -- a number of characters @c@, that encode for a single amino acid.+ | Frameshift+ { _frameshift ∷ !(Vector c)+ , _aa ∷ !aa+ }+ | Insert+ { _codon ∷ !(Codon c)+ , _aa ∷ !aa+ }+ | Shifted+ { _frameshift ∷ !(Vector c)+ , _aa ∷ !aa+ }+ | Region+ { _region ∷ !(Vector c)+ , _annotation ∷ !ByteString+ }+ | Delete+ {+ }+
LICENSE view
@@ -1,675 +1,30 @@- GNU GENERAL PUBLIC LICENSE- Version 3, 29 June 2007-- Copyright (C) 2007 Free Software Foundation, Inc. <http://fsf.org/>- Everyone is permitted to copy and distribute verbatim copies- of this license document, but changing it is not allowed.-- Preamble-- The GNU General Public License is a free, copyleft license for-software and other kinds of works.-- The licenses for most software and other practical works are designed-to take away your freedom to share and change the works. By contrast,-the GNU General Public License is intended to guarantee your freedom to-share and change all versions of a program--to make sure it remains free-software for all its users. We, the Free Software Foundation, use the-GNU General Public License for most of our software; it applies also to-any other work released this way by its authors. You can apply it to-your programs, too.-- When we speak of free software, we are referring to freedom, not-price. 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+ README.md view
@@ -0,0 +1,21 @@++++# BiobaseTypes++A bunch of types in use in different modules:++- numerical small and large numbers+- Gibbs free energy change+- phantom-typed linear indices: these encode the (rather annoying) habit of+ computational biology of having both 0-based and 1-based data++++#### Contact++Christian Hoener zu Siederdissen +Leipzig University, Leipzig, Germany +choener@bioinf.uni-leipzig.de +http://www.bioinf.uni-leipzig.de/~choener/ +
+ changelog.md view
@@ -0,0 +1,55 @@+0.2.1.0+-------++- CI/hackage github actions+- dependency updates++0.2.0.1+-------++- minor version bumped due to OrderedBits++0.2.0.0+-------++- unified treatment of bio sequences with one phantom-typed newtype.++0.1.4.0+-------++- changes to indexing and others+- some changes that probably require a bump++0.1.3.0+-------++- "biostring" wrappers (ByteString based RNA, DNA, ... sequences)++0.1.2.1+-------++- increased minimal required PrimitiveArray version+- removed almost all upper bounds+- removed ghc 7.8.4 as viable compiler++0.1.2.0+-------++- NFData instances++0.1.1.0+-------++- added Biobase.Types.Odds module (from the BiobaseBlast package)++0.1.0.0+-------++- re-introduced the types library for bioinformatics+- travis-ci integration++0.0.x,y+-------++- old variant; completely rewritten by now+
+ tests/properties.hs view
@@ -0,0 +1,134 @@++module Main where++import Control.Lens+import Debug.Trace+import qualified Data.ByteString.Char8 as BS8+import Test.QuickCheck.Modifiers+import Test.QuickCheck.Property ()+import Test.Tasty+import Test.Tasty.HUnit+import Test.Tasty.QuickCheck (testProperty)+import Test.Tasty.TH++import Biobase.Types.BioSequence+import Biobase.Types.Bitscore+import Biobase.Types.Location+import Biobase.Types.Shape+import Biobase.Types.Strand+import Biobase.Types.Structure+import Biobase.Types.Index as I++{-++-- * Bitscore conversions++prop_ProbScore (Positive null) (Positive x) = x ~= score2Prob null (prob2Score null x)++--prop_ScoreProb (Positive null) x = Bitscore x ~= prob2Score null (score2Prob null $ Bitscore x)++++-- * sequence properties++-- complement twice++prop_complement_twice_DNA (dna ∷ BioSequence DNA) = dna == dna^.complement.complement++prop_complement_twice_RNA (rna ∷ BioSequence RNA) = rna == rna^.complement.complement++prop_transcribe_twice_DNA (dna ∷ BioSequence DNA) = dna == dna^.transcribe.transcribe++--prop_transcribe_twice_DNA (rna ∷ RNAseq) = rna == rna^.transcribe.transcribe++-- * shape properties++-- ** unit tests for known rna secondary structures++-- ** quickcheck++-- | reversing a secondary structure means reversing the shape++prop_StructureShape_5_Reverse = fun_StructureShape_k_Reverse SL5+prop_StructureShape_4_Reverse = fun_StructureShape_k_Reverse SL4+prop_StructureShape_3_Reverse = fun_StructureShape_k_Reverse SL3+prop_StructureShape_2_Reverse = fun_StructureShape_k_Reverse SL2+prop_StructureShape_1_Reverse = fun_StructureShape_k_Reverse SL1++fun_StructureShape_k_Reverse lvl rnass@(RNAss s2)+ | shp == fshp = True+ | otherwise = traceShow (s2,shp,rshp,fshp) False+ where shp = rnass2shape lvl rnass+ rshp = rnass2shape lvl $ RNAss $ BS8.map flp $ BS8.reverse s2+ fshp = over rnashape (BS8.map flp . BS8.reverse) rshp+ flp '(' = ')'+ flp ')' = '('+ flp '[' = ']'+ flp ']' = '['+ flp x = x++prop_FwdLocationPlusTake (NonNegative (p ∷ Int), NonNegative (l ∷ Int), NonNegative (k ∷ Int))+ | check = True+ | otherwise = traceShow (p,l,k,fwdloc,taken,manual) check+ where fwdloc = FwdLocation PlusStrand (I.index p) l+ check = taken == manual+ taken = fwdLocationTake k fwdloc+ manual = FwdLocation PlusStrand (I.index p) (max 0 $ min l k)++prop_FwdLocationPlusDrop (NonNegative (p ∷ Int), NonNegative (l ∷ Int), NonNegative (k ∷ Int))+ | check = True+ | otherwise = traceShow (p,l,k,fwdloc,dropped,manual) check+ where fwdloc = FwdLocation PlusStrand (I.index p) l+ check = dropped == manual+ dropped = fwdLocationDrop k fwdloc+ manual = FwdLocation PlusStrand (I.index $ p + min l k) (max 0 $ l-k)++-- | Given a BioSequenceWindow, and different takes and drops, check wether what we have corresponds to what we want++case_bswTakeDrop ∷ Assertion+case_bswTakeDrop = do+ let wp = BioSequenceWindow @"DNA" @DNA "test" 1 "ACGTAC" 3 (FwdLocation PlusStrand 0 6)+ wm = BioSequenceWindow @"DNA" @DNA "test" 3 "CATGCA" 1 (FwdLocation MinusStrand 0 6)+ --+ bswTake 0 wp @?= BioSequenceWindow "test" 0 "" 0 (FwdLocation PlusStrand 0 0)+ bswTake 1 wp @?= BioSequenceWindow "test" 1 "A" 0 (FwdLocation PlusStrand 0 1)+ bswTake 2 wp @?= BioSequenceWindow "test" 1 "AC" 0 (FwdLocation PlusStrand 0 2)+ bswTake 6 wp @?= BioSequenceWindow "test" 1 "ACGTAC" 3 (FwdLocation PlusStrand 0 6)+ --+ bswDrop 0 wp @?= BioSequenceWindow "test" 1 "ACGTAC" 3 (FwdLocation PlusStrand 0 6)+ bswDrop 1 wp @?= BioSequenceWindow "test" 0 "CGTAC" 3 (FwdLocation PlusStrand 1 5)+ bswDrop 6 wp @?= BioSequenceWindow "test" 0 "" 0 (FwdLocation PlusStrand 6 0)+ --+ bswTake 0 wm @?= BioSequenceWindow "test" 0 "" 0 (FwdLocation MinusStrand 6 0)+ bswTake 1 wm @?= BioSequenceWindow "test" 1 "C" 0 (FwdLocation MinusStrand 5 1)+ bswTake 2 wm @?= BioSequenceWindow "test" 2 "CA" 0 (FwdLocation MinusStrand 4 2)+ bswTake 3 wm @?= BioSequenceWindow "test" 3 "CAT" 0 (FwdLocation MinusStrand 3 3)+ bswTake 4 wm @?= BioSequenceWindow "test" 3 "CATG" 0 (FwdLocation MinusStrand 2 4)+ bswTake 5 wm @?= BioSequenceWindow "test" 3 "CATGC" 0 (FwdLocation MinusStrand 1 5)+ bswTake 6 wm @?= BioSequenceWindow "test" 3 "CATGCA" 1 (FwdLocation MinusStrand 0 6)+ --+ bswDrop 0 wm @?= BioSequenceWindow "test" 3 "CATGCA" 1 (FwdLocation MinusStrand 0 6)+ bswDrop 1 wm @?= BioSequenceWindow "test" 2 "ATGCA" 1 (FwdLocation MinusStrand 0 5)+ bswDrop 2 wm @?= BioSequenceWindow "test" 1 "TGCA" 1 (FwdLocation MinusStrand 0 4)+ bswDrop 5 wm @?= BioSequenceWindow "test" 0 "A" 1 (FwdLocation MinusStrand 0 1)+ bswDrop 6 wm @?= BioSequenceWindow "test" 0 "" 0 (FwdLocation MinusStrand 0 0)+ --+ -- TODO consider having [take,take,drop,drop], generate all permutations;+ -- they should all yield the same result.+ --+++++-- * generic stuff++a ~= b = abs (b-a) <= 10e-6++main :: IO ()+main = $(defaultMainGenerator)++-}++main :: IO ()+main = return ()+