@@ -22358,6 +22358,39 @@ (define-public r-basics
groups of cells.")
(license license:gpl3)))
+(define-public r-basicstarrseq
+ (package
+ (name "r-basicstarrseq")
+ (version "1.30.0")
+ (source
+ (origin
+ (method url-fetch)
+ (uri (bioconductor-uri "BasicSTARRseq" version))
+ (sha256
+ (base32 "1dw6bv1qk2bn0l3m458sqgvm3s1karh4n3431pl7r0jj2r3mr6xa"))))
+ (properties `((upstream-name . "BasicSTARRseq")))
+ (build-system r-build-system)
+ (propagated-inputs
+ (list r-genomeinfodb
+ r-genomicalignments
+ r-genomicranges
+ r-iranges
+ r-s4vectors))
+ (native-inputs (list r-knitr))
+ (home-page "https://bioconductor.org/packages/BasicSTARRseq")
+ (synopsis "Basic peak calling on STARR-seq data")
+ (description
+ "This package implements a method that aims to identify enhancers on large
+scale. The STARR-seq data consists of two sequencing datasets of the same targets
+in a specifc genome. The input sequences show which regions where tested for
+enhancers. Significant enriched peaks i.e. a lot more sequences in one region
+than in the input where enhancers in the genomic DNA are, can be identified. So
+the approach pursued is to call peak every region in which there is a lot more
+(significant in a binomial model) STARR-seq signal than input signal and propose
+an enhancer at that very same position. Enhancers then are called weak or strong
+dependent of there degree of enrichment in comparison to input.")
+ (license license:lgpl3)))
+
(define-public r-basilisk-utils
(package
(name "r-basilisk-utils")