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-rw-r--r--gnu/packages/bioinformatics.scm184
1 files changed, 148 insertions, 36 deletions
diff --git a/gnu/packages/bioinformatics.scm b/gnu/packages/bioinformatics.scm
index 982cb7a984..4481235c78 100644
--- a/gnu/packages/bioinformatics.scm
+++ b/gnu/packages/bioinformatics.scm
@@ -84,6 +84,7 @@
#:use-module (gnu packages jemalloc)
#:use-module (gnu packages dlang)
#:use-module (gnu packages linux)
+ #:use-module (gnu packages lisp)
#:use-module (gnu packages logging)
#:use-module (gnu packages machine-learning)
#:use-module (gnu packages man)
@@ -1384,6 +1385,46 @@ gapped, local, and paired-end alignment modes.")
(supported-systems '("x86_64-linux"))
(license license:gpl3+)))
+(define-public bowtie1
+ (package
+ (name "bowtie1")
+ (version "1.2.2")
+ (source (origin
+ (method url-fetch)
+ (uri (string-append "mirror://sourceforge/bowtie-bio/bowtie/"
+ version "/bowtie-" version "-src.zip"))
+ (sha256
+ (base32
+ "1jl2cj9bz8lwz8dwnxbycn8yp8g4kky62fkcxifyf1ri0y6n2vc0"))
+ (modules '((guix build utils)))
+ (snippet
+ '(substitute* "Makefile"
+ ;; replace BUILD_HOST and BUILD_TIME for deterministic build
+ (("-DBUILD_HOST=.*") "-DBUILD_HOST=\"\\\"guix\\\"\"")
+ (("-DBUILD_TIME=.*") "-DBUILD_TIME=\"\\\"0\\\"\"")))))
+ (build-system gnu-build-system)
+ (arguments
+ '(#:tests? #f ; no "check" target
+ #:make-flags
+ (list "all"
+ (string-append "prefix=" (assoc-ref %outputs "out")))
+ #:phases
+ (modify-phases %standard-phases
+ (delete 'configure))))
+ (inputs
+ `(("tbb" ,tbb)
+ ("zlib" ,zlib)))
+ (supported-systems '("x86_64-linux"))
+ (home-page "http://bowtie-bio.sourceforge.net/index.shtml")
+ (synopsis "Fast aligner for short nucleotide sequence reads")
+ (description
+ "Bowtie is a fast, memory-efficient short read aligner. It aligns short
+DNA sequences (reads) to the human genome at a rate of over 25 million 35-bp
+reads per hour. Bowtie indexes the genome with a Burrows-Wheeler index to
+keep its memory footprint small: typically about 2.2 GB for the human
+genome (2.9 GB for paired-end).")
+ (license license:artistic2.0)))
+
(define-public tophat
(package
(name "tophat")
@@ -6240,6 +6281,48 @@ sequence.")
(supported-systems '("i686-linux" "x86_64-linux"))
(license license:bsd-3)))
+(define-public r-scde
+ (package
+ (name "r-scde")
+ (version "1.99.2")
+ (source (origin
+ (method git-fetch)
+ (uri (git-reference
+ (url "https://github.com/hms-dbmi/scde.git")
+ (commit version)))
+ (file-name (git-file-name name version))
+ (sha256
+ (base32
+ "10na2gyka24mszdxf92wz9h2c13hdf1ww30c68gfsw53lvvhhhxb"))))
+ (build-system r-build-system)
+ (propagated-inputs
+ `(("r-rcpp" ,r-rcpp)
+ ("r-rcpparmadillo" ,r-rcpparmadillo)
+ ("r-mgcv" ,r-mgcv)
+ ("r-rook" ,r-rook)
+ ("r-rjson" ,r-rjson)
+ ("r-cairo" ,r-cairo)
+ ("r-rcolorbrewer" ,r-rcolorbrewer)
+ ("r-edger" ,r-edger)
+ ("r-quantreg" ,r-quantreg)
+ ("r-nnet" ,r-nnet)
+ ("r-rmtstat" ,r-rmtstat)
+ ("r-extremes" ,r-extremes)
+ ("r-pcamethods" ,r-pcamethods)
+ ("r-biocparallel" ,r-biocparallel)
+ ("r-flexmix" ,r-flexmix)))
+ (home-page "https://hms-dbmi.github.io/scde/")
+ (synopsis "R package for analyzing single-cell RNA-seq data")
+ (description "The SCDE package implements a set of statistical methods for
+analyzing single-cell RNA-seq data. SCDE fits individual error models for
+single-cell RNA-seq measurements. These models can then be used for
+assessment of differential expression between groups of cells, as well as
+other types of analysis. The SCDE package also contains the pagoda framework
+which applies pathway and gene set overdispersion analysis to identify aspects
+of transcriptional heterogeneity among single cells.")
+ ;; See https://github.com/hms-dbmi/scde/issues/38
+ (license license:gpl2)))
+
(define-public r-centipede
(package
(name "r-centipede")
@@ -7127,28 +7210,6 @@ checks on R packages that are to be submitted to the Bioconductor repository.")
that accept short and long options.")
(license license:gpl2+)))
-(define-public r-dnacopy
- (package
- (name "r-dnacopy")
- (version "1.56.0")
- (source (origin
- (method url-fetch)
- (uri (bioconductor-uri "DNAcopy" version))
- (sha256
- (base32
- "04cqdqxhva66xwh1s2vffi56b9fcrqd4slcrvqasj5lp2rkjli82"))))
- (properties
- `((upstream-name . "DNAcopy")))
- (build-system r-build-system)
- (inputs
- `(("gfortran" ,gfortran)))
- (home-page "https://bioconductor.org/packages/DNAcopy")
- (synopsis "Implementation of a circular binary segmentation algorithm")
- (description "This package implements the circular binary segmentation (CBS)
-algorithm to segment DNA copy number data and identify genomic regions with
-abnormal copy number.")
- (license license:gpl2+)))
-
(define-public r-s4vectors
(package
(name "r-s4vectors")
@@ -11613,7 +11674,7 @@ Browser.")
(define-public bismark
(package
(name "bismark")
- (version "0.19.1")
+ (version "0.20.1")
(source
(origin
(method git-fetch)
@@ -11623,18 +11684,25 @@ Browser.")
(file-name (string-append name "-" version "-checkout"))
(sha256
(base32
- "0yb5l36slwg02fp4b1jdlplgljcsxgqfzvzihzdnphd87dghcc84"))
- (snippet
- '(begin
- ;; highcharts.js is non-free software. The code is available under
- ;; CC-BY-NC or proprietary licenses only.
- (delete-file "bismark_sitrep/highcharts.js")
- #t))))
+ "0xchm3rgilj6vfjnyzfzzymfd7djr64sbrmrvs3njbwi66jqbzw9"))))
(build-system perl-build-system)
(arguments
`(#:tests? #f ; there are no tests
+ #:modules ((guix build utils)
+ (ice-9 popen)
+ (srfi srfi-26)
+ (guix build perl-build-system))
#:phases
(modify-phases %standard-phases
+ ;; The bundled plotly.js is minified.
+ (add-after 'unpack 'replace-plotly.js
+ (lambda* (#:key inputs #:allow-other-keys)
+ (let* ((file (assoc-ref inputs "plotly.js"))
+ (installed "plotly/plotly.js"))
+ (let ((minified (open-pipe* OPEN_READ "uglify-js" file)))
+ (call-with-output-file installed
+ (cut dump-port minified <>))))
+ #t))
(delete 'configure)
(delete 'build)
(replace 'install
@@ -11653,10 +11721,11 @@ Browser.")
"deduplicate_bismark"
"filter_non_conversion"
"bam2nuc"
- "bismark2summary")))
+ "bismark2summary"
+ "NOMe_filtering")))
(substitute* "bismark2report"
- (("\\$RealBin/bismark_sitrep")
- (string-append share "/bismark_sitrep")))
+ (("\\$RealBin/plotly")
+ (string-append share "/plotly")))
(mkdir-p share)
(mkdir-p docdir)
(mkdir-p bin)
@@ -11665,8 +11734,8 @@ Browser.")
(for-each (lambda (file) (install-file file docdir))
docs)
(copy-recursively "Docs/Images" (string-append docdir "/Images"))
- (copy-recursively "bismark_sitrep"
- (string-append share "/bismark_sitrep"))
+ (copy-recursively "plotly"
+ (string-append share "/plotly"))
;; Fix references to gunzip
(substitute* (map (lambda (file)
@@ -11677,7 +11746,18 @@ Browser.")
"/bin/gunzip -c")))
#t))))))
(inputs
- `(("gzip" ,gzip)))
+ `(("gzip" ,gzip)
+ ("perl-carp" ,perl-carp)
+ ("perl-getopt-long" ,perl-getopt-long)))
+ (native-inputs
+ `(("plotly.js"
+ ,(origin
+ (method url-fetch)
+ (uri (string-append "https://raw.githubusercontent.com/plotly/plotly.js/"
+ "v1.39.4/dist/plotly.js"))
+ (sha256
+ (base32 "138mwsr4nf5qif4mrxx286mpnagxd1xwl6k8aidrjgknaqg88zyr"))))
+ ("uglify-js" ,uglify-js)))
(home-page "http://www.bioinformatics.babraham.ac.uk/projects/bismark/")
(synopsis "Map bisulfite treated sequence reads and analyze methylation")
(description "Bismark is a program to map bisulfite treated sequencing
@@ -13135,6 +13215,38 @@ descriptive settings file. The result is a set of comprehensive, interactive
HTML reports with interesting findings about your samples.")
(license license:gpl3+)))
+(define-public genrich
+ (package
+ (name "genrich")
+ (version "0.5")
+ (source (origin
+ (method git-fetch)
+ (uri (git-reference
+ (url "https://github.com/jsh58/Genrich.git")
+ (commit (string-append "v" version))))
+ (sha256
+ (base32
+ "0x0q6z0208n3cxzqjla4rgjqpyqgwpmz27852lcvzkzaigymq4zp"))))
+ (build-system gnu-build-system)
+ (arguments
+ `(#:tests? #f ; there are none
+ #:phases
+ (modify-phases %standard-phases
+ (delete 'configure)
+ (replace 'install
+ (lambda* (#:key outputs #:allow-other-keys)
+ (install-file "Genrich" (string-append (assoc-ref outputs "out") "/bin"))
+ #t)))))
+ (inputs
+ `(("zlib" ,zlib)))
+ (home-page "https://github.com/jsh58/Genrich")
+ (synopsis "Detecting sites of genomic enrichment")
+ (description "Genrich is a peak-caller for genomic enrichment
+assays (e.g. ChIP-seq, ATAC-seq). It analyzes alignment files generated
+following the assay and produces a file detailing peaks of significant
+enrichment.")
+ (license license:expat)))
+
(define-public mantis
(let ((commit "4ffd171632c2cb0056a86d709dfd2bf21bc69b84")
(revision "1"))