Source: trinityrnaseq Maintainer: Debian Med Packaging Team Uploaders: Michael R. Crusoe Section: science Priority: optional Build-Depends: debhelper-compat (= 13), jellyfish, libjung-free-java, javahelper, libgetopt-java, default-jdk, parafly, libjs-jquery, jaligner, libhts-dev, bowtie2, salmon, zlib1g-dev, cmake, r-bioc-edger, r-bioc-deseq2, r-bioc-rots, r-cran-fastcluster, liburi-perl, r-cran-ape, r-bioc-ctc, r-cran-gplots, r-cran-readr, r-bioc-biobase, r-bioc-qvalue, r-bioc-goseq, r-bioc-tximport, python3-htseq, rna-star, picard-tools, gmap, hisat2, subread, kallisto, python3-hisat2, r-cran-argparse, r-bioc-dexseq, tabix # r-cran-goplot, # r-bioc-glimma, # r-bioc-tximportdata Standards-Version: 4.5.1 Vcs-Browser: https://salsa.debian.org/med-team/trinityrnaseq Vcs-Git: https://salsa.debian.org/med-team/trinityrnaseq.git Homepage: https://trinityrnaseq.github.io/ Rules-Requires-Root: no Package: trinityrnaseq Architecture: any Depends: ${shlibs:Depends}, ${misc:Depends}, ${perl:Depends}, ${java:Depends}, bowtie, bowtie2, libwww-perl, default-jre-headless, samtools, jellyfish, r-base-core, r-cran-cluster, r-bioc-qvalue, rsem, berkeley-express, trimmomatic, transdecoder, parafly, curl, salmon, python3-numpy, ncbi-blast+, python3, r-cran-readr, r-bioc-edger, r-bioc-deseq2, r-bioc-rots, r-cran-fastcluster, liburi-perl, r-cran-ape, r-bioc-ctc, r-cran-gplots, r-bioc-biobase, r-bioc-goseq, r-bioc-tximport, python3-htseq, rna-star, gmap, hisat2, subread, kallisto, python3-hisat2, r-cran-argparse, r-cran-goplot, r-bioc-dexseq # r-bioc-glimma Recommends: ${java:Recommends}, trinityrnaseq-examples, r-cran-tidyverse, picard-tools, tabix Suggests: collectl, r-bioc-tximportdata Description: RNA-Seq De novo Assembly Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-seq reads. Trinity partitions the sequence data into many individual de Bruijn graphs, each representing the transcriptional complexity at a given gene or locus, and then processes each graph independently to extract full-length splicing isoforms and to tease apart transcripts derived from paralogous genes. Package: trinityrnaseq-examples Architecture: all Depends: ${perl:Depends}, ${java:Depends}, ${misc:Depends}, r-base-core Recommends: trinityrnaseq Description: RNA-Seq De novo Assembly common example and testing files Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-seq reads. Trinity partitions the sequence data into many individual de Bruijn graphs, each representing the transcriptional complexity at a given gene or locus, and then processes each graph independently to extract full-length splicing isoforms and to tease apart transcripts derived from paralogous genes. . This package contains testing & example files.