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A Clojure library designed to make the manipulation of biological sequence data easier.

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clj-biosequence

clj-biosequence is a library designed to make working with biological sequence data easier. Basic functions include:

  • Parses and accessors for Genbank, Uniprot XML, fasta and fastq formats.
  • A wrapper for BLAST.
  • A wrapper for signalP.
  • A wrapper for TMHMM.
  • Indexing of files for random access.
  • Mechanisms for lazy processing of sequences from very large files.
  • Interfaces for search and retrieval of sequences from online databases.
  • Translation functions for DNA and RNA sequences.
  • ID mapping functionality using the Uniprot's ID mapping tool.

Installation

Available from Clojars. For the current version add the following to your project.clj file:

[clj-biosequence "0.5.2"]

To use in your namespace:

(ns my-app.core
  (:require [clj-biosequence.core :as cbs] ;; for base functionality and fasta
  	        [clj-biosequence.uniprot :as up] ;; for Uniprot xml
	        [clj-biosequence.genbank :as gb] ;; for Genbank gbseq xml
	        [clj-biosequence.blast :as bl] ;; for BLAST functionality
            [clj-biosequence.fastq :as fq] ;; for fastq functionality
            [clj-biosequence.index :as ind] ;; for indexing functionality
	        [clj-biosequence.signalp :as sp] ;; for a wrapper for signalp
		[clj-biosequence.entrezgene :as ez] ;; for entrezgene xml
            [clj-biosequence.tmhmm :as tm])) ;; for a wrapper for TMHMM

The project page is here and there is also a guide to getting started with Clojure here.

API docs are available here.

Basic usage

clj-biosequence provides a reader and sequence mechanism for the lazy access of biosequences in a variety of formats. For example, if working with fasta sequences a typical session in the REPL could go something like:

;; import core and fasta functions

user> (use 'clj-biosequence.core)

;; To initialise a file call the relevant initialisation function,
;; a string or java file object can be used.
;; For fasta an alphabet is also required to initialise a file.

user> (def fa-file (init-fasta-file "test-files/nuc-sequence.fasta" :iupacNucleicAcids))
#'user/fa-file

;; then `bs-reader` can be used with `with-open` and `biosequence-seq`
;; to get access to a lazy sequence of fasta sequences in the file.

user> (with-open [r (bs-reader fa-file)]
                 (realized? (biosequence-seq r)))
false
user> (with-open [r (bs-reader fa-file)]
                 (count (biosequence-seq r)))
6

And thats just about it. The same pattern is used for all sequence formats supported (at the moment this includes Geneseq xml, Entrezgene xml, Uniprot xml, fasta and fastq formats).

Some examples:

;; a lazy sequence of translations in six reading frames

user> (with-open [r (bs-reader fa-file)]
                 (->> (biosequence-seq r)
                      (mapcat #(six-frame-translation %))
                      realized?))
false
user> (with-open [r (bs-reader fa-file)]
                 (->> (biosequence-seq r)
                      (mapcat #(six-frame-translation %))
                      count))
36

;; `fasta-string` can be used to convert biosequences to fasta strings

user> (use 'clj-biosequence.uniprot)
nil
user> (def uniprot-f (init-uniprotxml-file "test-files/uniprot-s-mansoni-20121217.xml"))
#'user/uniprot-f
user> (with-open [r (bs-reader uniprot-f)]
                 (println (->> (biosequence-seq r) first fasta-string)))

>sp|C4PYP8|DRE2_SCHMA Anamorsin homolog | Fe-S cluster assembly protein DRE2 homolog [Schistosoma mansoni]
MEQCVADCLNSDDCVMIVWSGEVQEDVMRGLQVAVSTYVKKLQFENLEKFVDSSAVDSQLXHECSVILCGWPNSISVNILK
LGLLSNLLSCLRPGGRFFGRDLITGDWDSLKKNLTLSGYIXNPYQLSCENHLIFSASVPSNYTQGSSVKLPWANSDVEAAW
ENVDNSSDANGNIINTNTLLXQKSDLKTPLSVCGKEAATDSVGKKKRACKNCTCGLAEIEAAEEDKSDVPISSCGNCYLGD
XAFRCSTCPYRGLPPFKPGERILIPDDVLRADL

;; filters can be implemented pretty easily

user> (with-open [r (bs-reader fa-file)]
                 (->> (biosequence-seq r)
                      (filter #(second (re-find #"(Mus musculus)" (def-line %))))
                      first
                      accession))
"gi|114311762|gb|EE738912.1|EE738912"

;; The function `biosequence->file` sends biosequences to a file and
;; also accepts a function argument to transform the biosequence
;; before writing (the default is `fasta-string`).

;; a Uniprot to fasta converter is thus:

user> (with-open [r (bs-reader uniprot-f)]
                 (biosequence->file (biosequence-seq r)
		                     "/tmp/fasta.fa"))
"/tmp/fasta.fa"
user> (with-open [r (bs-reader (init-fasta-file "/tmp/fasta.fa"
                               :iupacAminoAcids))]
                 (count (biosequence-seq r)))
2
user> (with-open [r (bs-reader (init-fasta-file "/tmp/fasta.fa"
                                                :iupacAminoAcids))]
                 (class (first (biosequence-seq r))))
clj_biosequence.core.fastaSequence

;; sequences can be filtered to file using this function
;; for eg. filter Cytoplasmic proteins to file in fasta format

user> (with-open [r (bs-reader uniprot-f)]
                 (biosequence->file
                  (->> (biosequence-seq r)
                       (filter #(some (partial = "Cytoplasm")
                           (map :text (subcellular-location %)))))
                  "/tmp/fasta.fa"))
"/tmp/fasta.fa"
user> (with-open [r (bs-reader (init-fasta-file "/tmp/fasta.fa" :iupacAminoAcids))]
                 (count (biosequence-seq r)))
1
user> (with-open [r (bs-reader (init-fasta-file "/tmp/fasta.fa" :iupacAminoAcids))]
                 (println (fasta-string (first (biosequence-seq r)))))
>sp|C4PYP8|DRE2_SCHMA Anamorsin homolog | Fe-S cluster assembly protein DRE2 homolog [Schistosoma mansoni]
MEQCVADCLNSDDCVMIVWSGEVQEDVMRGLQVAVSTYVKKLQFENLEKFVDSSAVDSQLXHECSVILCGWPNSISVNILK
LGLLSNLLSCLRPGGRFFGRDLITGDWDSLKKNLTLSGYIXNPYQLSCENHLIFSASVPSNYTQGSSVKLPWANSDVEAAW
ENVDNSSDANGNIINTNTLLXQKSDLKTPLSVCGKEAATDSVGKKKRACKNCTCGLAEIEAAEEDKSDVPISSCGNCYLGD
XAFRCSTCPYRGLPPFKPGERILIPDDVLRADL

For strings containing fasta, Uniprot XML or Genbank XML formatted sequences the functions init-fasta-string, init-uniprot-string and init-genbank-string allow the use of strings with the with-open idiom. For Uniprot and Genbank connection initialisation functions provide the same capability with remotely stored sequences from the relevant servers (see below).

Indexing

For random access to biosequences each supported file format also has an indexed version.

Typical usage as follows:

;; calling `index-biosequence-file` on any biosequence file returns a
;; biosequence index. Which is accessed using `with-open` just like 
;; other readers but with faster retrieval of specific biosequences.

user> (use 'clj-biosequence.index)
nil
user> (def fasta-in (index-biosequence-file fa-file))
#'user/fasta-in
user> (with-open [r (bs-reader fasta-in)]
        (count (biosequence-seq r))
6
user> (with-open [r (bs-reader fasta-in)]
        (first (biosequence-seq r))
#clj_biosequence.core.fastaSequence{:acc "gi|116025203|gb|EG339215.1|EG339215", :description "KAAN-aaa29f08.b1 ... etc"

user> (with-open [r (bs-reader fasta-in)]
        (accession (get-biosequence r "gi|114311762|gb|EE738912.1|EE738912"))
"gi|114311762|gb|EE738912.1|EE738912"

;; when a file is indexed two additional files are created with the same
;; base-name as the biosequence file but with the extensions `.bin` and `.idx`.
;; The `.bin` file is compressed sequences and the `.idx` file is a 
;; text file containing the index. The `.idx` file is readable with
;; edn/read-string. To load an index use `load-biosequence-index` with the
;; path and basename of the index files.

user> (def fa-ind-2 (load-biosequence-index "/Users/jason/Dropbox/clj-biosequence/resources/test-files/nuc-sequence.fasta"))
#'user/fa-ind-2
user> (with-open [r (bs-reader fa-ind-2)]
        (accession (get-biosequence r "gi|114311762|gb|EE738912.1|EE738912"))
"gi|114311762|gb|EE738912.1|EE738912"

;; biosequence collections can be indexed using `index-biosequence-list`.

user> (def fa-ind-3 (with-open [r (bs-reader fa-file)]
                      (index-biosequence-list (biosequence-seq r)
                                              "/tmp/fasta-ind")))
#'user/fa-ind-3
user> (with-open [r (bs-reader fa-ind-3)]
        (accession (get-biosequence r "gi|114311762|gb|EE738912.1|EE738912"))
"gi|114311762|gb|EE738912.1|EE738912"

;; this can be handy when filtering biosequences. For example secreted proteins
;; can be filtered into their own index

user> (def secreted (with-open [r (bs-reader toxins)]
                               (index-biosequence-list (-> (take 20 (biosequence-seq r))
                                                           (filter-signalp :trim true))
                                                       "/tmp/secreted-ind")))
#'user/secreted
user> (with-open [r (bs-reader fa-ind-3)]
        (count (biosequence-seq r))
6

BLAST

clj-biosequence supports most forms of BLAST, with the exception of PSI-BLAST. As with other parts of clj-biosequence the BLAST functions seek to be as lazy and composable as possible. To work the various BLAST+ programs from the NCBI need to be in your path.

Typical usage as follows:

;; initialise a BLAST db by passing the basename of the indexes to `init-blast-db`

user> (use 'clj-biosequence.blast)
nil
user> (def toxindb (init-blast-db "test-files/toxins.fasta" :iupacAminoAcids))
#'user/toxindb

;; The function`blast` takes a list of biosequence objects and blasts them against
;; a blast database. It returns a blast search result which is a pointer to the
;; blast result file. This can then be opened using `bs-reader` and results
;; accessed using `biosequence-seq`

user> (def tox-bl (with-open [r (bs-reader toxins)]
                             (blast (take 20 (biosequence-seq r))
                                    "blastp"
                                    toxindb
                                    "/tmp/blast.xml")))
#'user/tox-bl
user> (with-open [r (bs-reader tox-bl)]
                 (count (biosequence-seq r)))
20

;; Addiitonal parameters can be passed to `blast` using the `:param` keyword
;; argument. Format is a hash-map with keys strings of the command line switches
;; with the desired value as a string. For example:

user> (def tox-bl (with-open [r (bs-reader toxins)]
                             (blast (take 20 (biosequence-seq r))
                                    "blastp"
                                    toxindb
                                    "/tmp/blast.xml"
                                    :params {"-max_target_seqs" "3"
                                             "-evalue" "1"})))
#'user/tox-bl

;; BLAST results can be accessed using the accessors defined in the package
;; and the functions `hit-seq` and `hsp-seq`. For example to filter all
;; proteins in `tox-bl` that had a hit with a bit-score greater than
;; 50 and report their accession (note the use of second to avoid hits
;; to themselves):

user> (with-open [r (bs-reader tox-bl)]
                 (doall (->> (biosequence-seq r)
                             (filter #(>= (-> (hit-seq %) second hit-bit-scores first) 50))
                             (map #(-> (hit-seq %) second hit-accession))))
("B3EWT5" "Q5UFR8" "C1IC47" "Q53B61" "O76199" "C0JAT6" "P0CE79" "C0JAU1" "C0JAT6" "P0CE78"
"C0JAT9" "C0JAT5" "C0JAT9" "C0JAT6" "P0CE81" "P0CE80" "P0CE81" "P0CE82" "P0CE81")

;; Or a hash-map of the query id and  hit id of hits with a bit score greater than 50
;; (note that calling `accession` on a BLAST iteraton returns the query accession):

user> (with-open [r (bs-reader tox-bl)]
                 (->> (biosequence-seq r)
                      (filter #(>= (-> (hit-seq %) second hit-bit-scores first) 50))
                      (map #(vector (accession %)
                                    (-> (hit-seq %) second hit-accession)))
                      (into {}))))
{"sp|P84001|29C0_ANCSP" "B3EWT5", "sp|P0CE81|A1HB1_LOXIN" "P0CE80", "sp|C0JAT9|A1H1_LOXSP"
"C0JAU1", "sp|P0CE82|A1HB2_LOXIN" "P0CE81", "sp|P0CE80|A1HA_LOXIN" "P0CE81",
"sp|C0JAT8|A1H4_LOXHI" "C0JAT6", "sp|C0JAT5|A1H2_LOXHI" "C0JAT6", "sp|C0JAT6|A1H3_LOXHI"
"C0JAT5", "sp|C0JAT4|A1H1_LOXHI" "C0JAT6", "sp|C0JAU1|A1H2_LOXSP" "C0JAT9",
"sp|C0JAU2|A1H3_LOXSP" "C0JAT9", "sp|Q4VDB5|A1H_LOXGA" "P0CE82", "sp|C1IC47|3FN3_WALAE"
"Q5UFR8", "sp|C1IC48|3FN4_WALAE" "C1IC47", "sp|C1IC49|3FN5_WALAE" "Q53B61",
"sp|P84028|45C1_ANCSP" "O76199", "sp|Q56JA9|A1H_LOXSM" "P0CE81", "sp|P0CE78|A1H1_LOXRE"
"P0CE79", "sp|P0CE79|A1H2_LOXRE" "P0CE78"}

;; This can be combined with indexes or biosequence files to obtain the original
;; query biosequences.

user> (def toxin-index (index-biosequence-file toxins))
#'user/toxin-index

user> (with-open [r (bs-reader tox-bl)
                  i (bs-reader toxin-index)]
                 (->> (biosequence-seq r)
                      (filter #(>= (-> (hit-seq %) second hit-bit-scores first) 50))
                      (map #(get-biosequence i (accession %)))
                      first))
#clj_biosequence.core.fastaSequence{:acc "sp|P84001|29C0_ANCSP", :description
"U3-ctenitoxin-Asp1a (Fragment) OS=Ancylometes sp. PE=1 SV=1", :alphabet :iupacAminoAcids,
:sequence [\A \N \A \C \T \K \Q \A \D \C \A \E \D \E \C \C \L \D \N \L \F \F \K \R \P \Y
\C \E \M \R \Y \G \A \G \K \R \C \A \A \A \S \V \Y \K \E \D \K \D \L \Y]}

;; or sent off to a file.

user> (with-open [r (bs-reader tox-bl)
                  i (bs-reader toxin-index)]
                 (biosequence->file
                  (->> (biosequence-seq r)
                       (filter #(>= (-> (hit-seq %) second hit-bit-scores first) 50))
                       (map #(get-biosequence i (accession %))))
                  "/tmp/blast.fa"))
"/tmp/blast.fa"

;; As the entire chain is lazy these methods will work with as big a file as
;; can be thrown at them (hopefully). So one could annotate a large fasta file
;; starting with a fasta index and a blast DB by:

user> (with-open [r (bs-reader (blast (biosequence-seq toxin-index) "blastp" toxindb
                                      "/tmp/outfile.xml"))
	          i (bs-reader toxin-index)]
                 (biosequence->file
                  (->> (biosequence-seq r)
                       (filter #(>= (-> (hit-seq %) second hit-bit-scores first) 50))
                       (map #(let [s (get-biosequence i (accession %))
                                   h (-> (hit-seq %) first)]
                               (assoc s :description
                                      (str (def-line s) " - "
                                           "Similar to " (hit-def h) " - "
                                           (first (hit-bit-scores h)))))))
                  "/tmp/annotated-sequeunces.fa"))
"/tmp/annotated-sequeunces.fa"
user> (with-open [r (bs-reader (init-fasta-file "/tmp/annotated-sequeunces.fa"
                                                :iupacAminoAcids))]
                 (println (def-line (first (biosequence-seq r)))))
U3-ctenitoxin-Asp1a (Fragment) OS=Ancylometes sp. PE=1 SV=1 - Similar to Toxin CSTX-20 \
OS=Cupiennius salei PE=1 SV=1 - 89.737335

;; Although this is getting a bit complicated for the REPL and should probably
;; be a function(s) of itself (and the blast outfile might need to be deleted).

;; BLAST readers also provide access to the parameters used and these
;; can be accessed by calling `parameters` on the reader. This will return a
;; blast parameters object with accessors defined in the package.

user> (with-open [r (bs-reader tox-bl)]
                 (blast-database (parameters r)))
"/Users/jason/Dropbox/clj-biosequence/resources/test-files/toxins.fasta"
user> (with-open [r (bs-reader tox-bl)]
                 (blast-version (parameters r)))
"BLASTP 2.2.24+"
user> (with-open [r (bs-reader tox-bl)]
                 (blast-evalue (parameters r)))
"10"
user> (with-open [r (bs-reader tox-bl)]
                 (blast-filter (parameters r)))
"F"

;; BLAST searches can be indexed like any other biosequence file. In which case
;; the index is keyed to the query accession. Although, the parameter information
;; is lost.

user> (def blast-ind (index-biosequence-file tox-bl))
#'user/blast-ind
user> (-> (get-biosequence blast-ind "sp|Q56JA9|A1H_LOXSM") hit-seq first hit-accession)
"P0CE82"

SignalP

SignalP works in a similar way as BLAST. If you have signalp in your path it can be applied to collections of bioseqeunces using the function signalp (which returns a signalp result object) or a SignalP output file in short form format can be initialised as a result object.

Basic usage as follows:

;; running signalp

user> (use 'clj-biosequence.signalp)
nil
user> (def sr (signalp (take 20 (biosequence-seq toxin-index)) "/tmp/signalp.txt"))
#'user/sr
user> (with-open [r (bs-reader sr)]
                 (first (biosequence-seq r)))
#clj_biosequence.signalp.signalpProtein{:name "sp|P58809|CTX_CONMR", :cmax 0.105,
:cpos 7, :ymax 0.147, :ypos 1, :smax 0.208, :spos 1, :smean 0.0, :D 0.068, :result "N",
:Dmaxcut 0.45, :network "SignalP-noTM"}
user> (with-open [r (bs-reader sr)]
                 (accession (first (biosequence-seq r))))
"sp|P58809|CTX_CONMR"

;; `signalp?` can be used to determine if a result is positive or not

user> (with-open [r (bs-reader sr)]
                 (signalp? (first (biosequence-seq r))))
false
user> (with-open [r (bs-reader sr)]
                 (-> (filter signalp? (biosequence-seq r))
                     first))
#clj_biosequence.signalp.signalpProtein{:name "sp|Q9BP63|O3611_CONPE", :cmax 0.51,
:cpos 21, :ymax 0.696, :ypos 21, :smax 0.982, :spos 12, :smean 0.952, :D 0.834,
:result "Y", :Dmaxcut 0.45, :network "SignalP-noTM"}

;; a convenience function `filter-signalp` filters a collection of biosequence
;; proteins and returns only proteins containing a signal sequence. If the
;; keyword argument `:trim` is true the returned biosequences will have the
;; signal sequence trimmed from the sequence

user> (->> (filter-signalp (take 20 (biosequence-seq toxin-index)))
           first
           bioseq->string)
"MSRLGIMVLTLLLLVFIVTSHQDAGEKQATQRDAINFRWRRSLIRRTATEECEEYCEDEEKTCCGLEDGEPVCATTCLG"
user> (->> (filter-signalp (take 20 (biosequence-seq toxin-index)) :trim true)
           first
           bioseq->string)
"DAGEKQATQRDAINFRWRRSLIRRTATEECEEYCEDEEKTCCGLEDGEPVCATTCLG"

;; SignalP result objects can be indexed in the same manner as BLAST ie.
;; the query sequence accession becomes the index keys.

user> (def si (index-biosequence-file sr))
#'user/si
user> (accession (get-biosequence si "sp|P58809|CTX_CONMR"))
"sp|P58809|CTX_CONMR"
user> (signalp? (get-biosequence si "sp|P58809|CTX_CONMR"))
false

;; Search parameters can be passed to `signalp` and `filter-signalp` as hash-maps
;; using the `:param` keyword argument.

user> (def sr (signalp (take 20 (biosequence-seq toxin-index)) "/tmp/signalp.txt"
                       :params {"-s" "best" "-t" "gram+"}))
#'user/sr
user> (with-open [r (bs-reader sr)]
                 (first (biosequence-seq r)))
#clj_biosequence.signalp.signalpProtein{:name "sp|P58809|CTX_CONMR", :cmax 0.101,
:cpos 2, :ymax 0.119, :ypos 2, :smax 0.139, :spos 1, :smean 0.139, :D 0.127,
:result "N", :Dmaxcut 0.45, :network "SignalP-TM"}

Accession mapping

clj-biosequence provides a facility for mapping accessions from one database to another. It is provided in the core package and uses the Uniprot mapping service so needs an active internet connection.

Basic usage:

;; `id-convert` converts accessions. Its arguments are a list of accessions
;; to be converted, a 'from' database, a 'to' database and an email (required
;; by Uniprot). The 'from' and 'to' arguments are strings corresponding to
;; to the database codes used by the Uniprot mapping tool (full list at
;; http://www.uniprot.org/faq/28#id_mapping_examples and a partial list in
;; the doc string of `id-convert`.

;; `id-convert` returns a hash-map of query accessions and search results. If
;; an ID returned no result it is not in the result hash-map. There is a
;; 100,000 limit on individual queries imposed by Uniprot.

;; For example, to convert a list of Uniprot accessions to NCBI Genbank ids, 
;; using the previously defined toxin protein index which has accessions in
;; the format "sp|xxx|xxxx":

user> (map accession (take 5 (biosequence-seq toxin-index)))
("sp|P58809|CTX_CONMR" "sp|P61792|TXU2_HETVE" "sp|P86259|CT2X_CONTE"
"sp|Q9BP63|O3611_CONPE" "sp|A0SE59|CA13_CONMR")

user> (require '[clojure.string :as st])
nil
user> (-> (map #(second (st/split (accession %) #"\|"))
                (take 5 (biosequence-seq toxin-index)))
          (id-convert "ACC" "P_GI" "[email protected]"))
{"P58809" "20454877", "P61792" "48428590", "P86259" "229485330", "Q9BP63" "74848505",
"A0SE59" "83657225"}

Sequence retrieval

Sequences can be retrieved from both Genabnk and Uniprot using init-uniprot-connection and init-genbank-connection. Both functions take a list of accession numbers and a return type argument. Uniprot also needs and email argument and Genbank a database argument. Both functions can be used in conjunction with the search functions, genbank-search and uniprot-search.

Basic usage:

;; To generate a list of accessions search for Uniprot accessions (note this
;; generates a non-lazy list). Search syntax is exactly the same as Uniprot
;; search syntax (described at http://www.uniprot.org/help/text-search and
;; summarised in the doc string of `uniprot-search`).

;; For example, to get accessions of all proteins in the Schistosoma mansoni
;; reference proteome set:

user> (use 'clj-biosequence.uniprot)
nil
user> (def sm-prot (uniprot-search "organism:6183 AND keyword:1185" "[email protected]"))
#'user/sm-prot
user> (count sm-prot)
11711
user> (first sm-prot)
"C4PYP8"

;; A lazy sequence of biosequences can be retrieved from Uniprot using
;; `init-uniprot-connection` and `bs-reader`. Sequences can be retrieved as
;; fasta or full Uniprot entries.

user> (def up-conn (init-uniprot-connection (take 10 sm-prot) :fasta "[email protected]"))
#'user/up-conn
user> (with-open [r (bs-reader up-conn)]
                 (first (biosequence-seq r)))
#clj_biosequence.core.fastaSequence{:acc "sp|C4PYP8|DRE2_SCHMA", :description\
"Anamorsin homolog OS=Schistosoma mansoni GN=Smp_207000 PE=3 SV=2", :alphabet\
:iupacAminoAcids, :sequence [\M \E \Q \C \V \A \D \C \L \N \S \D \D \C \V \M ... etc

;; Uniprot

user> (def up-conn (init-uniprot-connection (take 10 sm-prot) :xml "[email protected]"))
#'user/up-conn
user> (with-open [r (bs-reader up-conn)]
                 (class (first (biosequence-seq r))))
clj_biosequence.uniprot.uniprotProtein

;; Although sequences are downloaded as a compressed stream large sequence
;; downloads can take a long time ...

;; Genbank works exactly the same way. Search syntax is the same as Genbank query
;; format (see http://www.ncbi.nlm.nih.gov/books/NBK3837/ and a summary in the doc
;; doc string of `genbank-search`). A database also neds to specified and may be one
;; of :protein, :nucest, :nuccore, :nucgss or :popset.

;; So to get all Schistosoma mansoni proteins from Genbank

user> (use 'clj-biosequence.genbank)
nil
user> (def sm-prots (genbank-search "txid6183[Organism:noexp]" :protein))
#'user/sm-prots
user> (first sm-prots)
"566601372"
user> (with-open [r (bs-reader (init-genbank-connection (take 10 sm-prots) :protein :fasta))]
                 (second (biosequence-seq r)))
#clj_biosequence.core.fastaSequence{:acc "gi|566601352|gb|AHC70335.1|", :description
"nicotinic acetylcholine receptor [Schistosoma mansoni]", :alphabet :iupacAminoAcids,
:sequence [\M ... etc

user> (with-open [r (bs-reader (init-genbank-connection (take 10 sm-prots) :protein :xml))]
                 (class (second (biosequence-seq r))))
clj_biosequence.genbank.genbankSequence

Supported formats

clj-biosequence uses protocols and records to provide a uniformish interface to diferent formats.

Fasta

;; initialise fasta files using `init-fasta-file` and access
;; sequences using `bs-reader` and `biosequence-seq`

user> (def ff (init-fasta-file "test-files/toxins.fasta" :iupacAminoAcids))

user> (with-open [r (bs-reader ff)]
	(count (biosequence-seq r)))
5135
user> 

;; records and protocols implemented by them as follows:

->fastaSequence
Implements: biosequenceID
	    biosequenceDescription
	    Biosequence

Fastq

;; Use `init-fastq-file` and access sequences as above.

user> (def ff (init-fastq-file "test-files/fastq-test.fastq"))
#'user/ff
user> (with-open [r (bs-reader ff)]
	(count (biosequence-seq r)))
9
user> 

;; records and protocols as follows:

->fastqSequence
Implements: biosequenceID
	    biosequenceDescription
	    Biosequence

Uniprot

;; initialise uniprot files using `init-uniprotxml-file` and access
;; sequences as described above

user> (def up (init-uniprotxml-file "test-files/uniprot-s-mansoni-20121217.xml"))
#'user/up
user> (with-open [r (bs-reader up)]
                 (count (biosequence-seq r)))
2

;; records and protocols implemented by them are as follows:

->uniprotProtein ;; top level record for uniprot sequences
Implements: Biosequence
	    biosequenceID
	    biosequenceName
	    biosequenceDescription
	    biosequenceCitations ;; returns uniprotCitation records
	    biosequenceFeatures ;; returns uniprotFeature records
	    biosequenceTaxonomies ;; returns uniprotTaxref records
	    biosequenceGenes ;; returns uniprotGene records
	    biosequenceComments ;; returns uniprotComment records
	    biosequenceSubcelllocs ;; returns uniprotFeature records containg sub celllar location data
	    biosequenceGoterms ;; returns uniprotFeature records containg GO data
	    biosequenceEvidence
	    biosequenceProtein	
->uniprotComment
Implements: biosequenceSubcellloc
	    biosequenceSubcellloc
->uniprotGene
Implements: biosequenceGene
	    biosequenceID
	    biosequenceSynonyms
->uniprotTaxref
Implements: biosequenceTaxonomy
	    biosequenceDbrefs
	    biosequenceEvidence
->uniprotDbref
Implements: biosequenceDbref
	    biosequenceGoterm
	    biosequenceEvidence
->uniprotFeature
Implements: biosequenceNameobject
	    biosequenceID
	    biosequenceStatus
	    biosequenceDescription
	    biosequenceEvidence
	    biosequenceCitations
	    biosequenceIntervals
	    Biosequence
	    biosequenceVariant
->uniprotInterval
Implements: biosequenceInterval
	    biosequenceStatus
	    biosequenceEvidence
->uniprotCitation
Implements: biosequenceCitation

;; some examples

user> (with-open [r (bs-reader up)]
        (-> (biosequence-seq r) first tax-refs first lineage))
"Eukaryota;Metazoa;Platyhelminthes;Trematoda;Digenea;Strigeidida;Schistosomatoidea;Schistosomatidae;Schistosoma"

user> (with-open [r (bs-reader up)]
                 (-> (biosequence-seq r) first alternate-names))
"Fe-S cluster assembly protein DRE2 homolog"

user> (with-open [r (bs-reader up)]
                 (-> (biosequence-seq r) second citations first authors))
("Berriman M." "Haas B.J." "LoVerde P.T." "Wilson R.A." "Dillon G.P." "Cerqueira G.C." ...)

user> (with-open [r (bs-reader up)]
                 (-> (biosequence-seq r) second feature-seq first obj-type))
"chain"

GenBank: Geneseq xml

;; initialise a genbank file in the usual way

user> (def gbf (init-genbank-file "test-files/nucleotide-gb.xml"))
#'user/gbf

;; Access sequences as usual

user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first tax-refs first
		     get-db-refs first object-id))
1268274

;; records and protocols as follows:
->genbankSequence ;; the top level record for Geneseq sequences
Implements: biosequenceGene
	    biosequenceID
	    biosequenceDescription
	    Biosequence
	    biosequenceCitations ;; returns citation records
	    biosequenceFeatures ;; returns feature records
	    biosequenceTaxonomies ;; returns tax-ref records
->genbankTaxRef
Implements: biosequenceTaxonomy
	    biosequenceFeatures
	    biosequenceDbrefs ;; returns db records
->genbankFeature
Implements: biosequenceFeature
	    biosequenceGene
	    biosequenceID
	    biosequenceProtein
	    biosequenceEvidence
	    biosequenceNotes
	    biosequenceNameobject
	    biosequenceIntervals ;; returns interval records
	    biosequenceDbrefs ;; returns db records
->genbankDbRef
Implements: biosequenceDbref
->genbankQualifier
Implements: biosequenceNameObject
->genbankInterval
Implements: biosequenceID
	    biosequenceInterval
	    biosequenceTranslation
->genbankCitation
Implements: biosequenceCitation
	    biosequenceNotes
->genbankReader
Implements: biosequenceReader
->genbankFile
Implements: biosequenceIO
	    biosequenceFile

;; some examples

user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first locus))
"KE373594"

user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first feature-seq
		     first obj-type))
"source"
user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first feature-seq first
		     intervals first start))
1

;; The function `qualifiers` is also provided for genbank features
;; and it returns a lazy list of qualifiers.

user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first feature-seq first
		     qualifiers first obj-type))
"organism"
user> (with-open [r (bs-reader gbf)]
                 (-> (biosequence-seq r) first feature-seq first
                     qualifiers first obj-value))
"Blumeria graminis f. sp. tritici 96224"

GenBank: Entrezgene xml

Access sequences in the usual way:

user> (use 'clj-biosequence.entrezgene)
nil
user> (def ef (init-entrezgene-file "test-files/entrez-gene.xml"))
#'user/ef
user> (with-open [r (bs-reader ef)]
	(-> (biosequence-seq r)
	    first
	    accession))
3875
user> 

;; records and protocols as follows:

->entrezGene ;; top level record for an entrez gene
Implements: biosequenceGene
	    biosequenceSynonyms
	    biosequenceDescription
	    biosequenceDbrefs ;; returns db records
	    biosequenceComments ;; returns comment records
	    entrezComments
	    biosequenceTranslation
	    biosequenceID
	    biosequenceStatus
	    biosequenceSummary
	    biosequenceTaxonomies ;; returns tax-ref records
	    biosequenceProteins ;; return protein sub-seq records
	    Biosequence
->entrezProtein
Implements: biosequenceProtein
	    biosequenceSynonyms
	    biosequenceDescription
	    biosequenceDbrefs ;; reurns db records
->entrezBiosource
->entrezPcrPrimers
->entrezSubSource
->entrezOrgRef
Implements: biosequenceTaxonomy
	    biosequenceDbrefs ;; returns db records
	    biosequenceSynonyms
->entrezOrgName
->entrezGeneTrack
Implements: biosequenceID
	    biosequenceStatus
->entrezMap
->entrezGeneSource
->entrezGeneComment
Implements: biosequenceID
	    entrezComments
	    biosequenceComments ;; returns comment records
	    biosequenceNameObject
->entrezExtraterm
Implements: biosequenceNameObject
->entrezOtherSource
Implements: biosequenceUrl
	    biosequenceDbrefs
->entrezDbtag
Implements: biosequenceDbref
->entrezSeqLocation
Implements: biosequenceIntervals ;; returns interval records
->entrezInterval
Implements: biosequenceInterval
->entrezGeneReader
Implements: biosequenceReader
->entrezgeneFile
Implements: biosequenceIO
	    biosequenceFile
->entrezGeneConnection
Implements: biosequenceIO

License

Copyright © 2015 Jason Mulvenna

Distributed under the Eclipse Public License either version 1.0 or (at your option) any later version.

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A Clojure library designed to make the manipulation of biological sequence data easier.

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