pinfish 0.1.0+ds-4 source package in Ubuntu

Changelog

pinfish (0.1.0+ds-4) unstable; urgency=medium

  * Team upload.
  * Cleanup bam files from dh_auto_test
    Closes: #1048260
  * Standards-Version: 4.6.2 (routine-update)
  * Remove trailing whitespace in debian/copyright (routine-update)
  * Remove trailing whitespace in debian/rules (routine-update)
  * No tab in license text (routine-update)
  Add missing ${misc:Built-Using} to Built-Using on pinfish.
  Apply multi-arch hints.

   + pinfish-examples: Add Multi-Arch: foreign.


 -- Andreas Tille <email address hidden>  Fri, 12 Jan 2024 07:23:48 +0100

Upload details

Uploaded by:
Debian Med
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any all
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Oracular release universe misc
Noble release universe misc

Downloads

File Size SHA-256 Checksum
pinfish_0.1.0+ds-4.dsc 2.5 KiB 36d8ac12d7da5669a1c18f2f10695e99d81073d2066294e3ed23a110dbba69f6
pinfish_0.1.0+ds.orig-debian-tests-data.tar.xz 65.4 MiB 40957e398ab9bebdc89fe69dbef1c816da544e69a6aeed9c04371430f61f53bb
pinfish_0.1.0+ds.orig.tar.xz 4.8 MiB c8213acc3f88d9e1294b9f9014a28b8fd410ebe0aab4793c7bb7263e7e465e4d
pinfish_0.1.0+ds-4.debian.tar.xz 6.4 KiB 244fe376c04deed5bbf98824576c5cfc7d2b819e1a7a595bf90207573681312d

Available diffs

No changes file available.

Binary packages built by this source

pinfish: Collection of tools to annotate genomes using long read transcriptomics data

 The toolchain is composed of the following tools:
 1. spliced_bam2gff - a tool for converting sorted BAM
 files containing spliced alignments
 into GFF2 format. Each read will be represented as a distinct
 transcript. This tool comes handy when visualizing spliced
 reads at particular loci and to provide input to the rest
 of the toolchain.
 .
 2. cluster_gff - this tool takes a sorted GFF2 file as
 input and clusters together reads having similar
 exon/intron structure and creates a rough consensus
 of the clusters by taking the median of exon
 boundaries from all transcripts in the cluster.
 .
 3. polish_clusters - this tool takes the cluster
 definitions generated by cluster_gff and for each
 cluster creates an error corrected read by mapping
 all reads on the read with the median length
 and polishing it using racon. The polished reads
 can be mapped to the genome using minimap2 or GMAP.
 .
 4. collapse_partials - this tool takes GFFs generated
 by either cluster_gff or polish_clusters and filters
 out transcripts which are likely to be based on RNA
 degradation products from the 5' end. The tool clusters
 the input transcripts into "loci" by the 3' ends and
 discards transcripts which have a compatible transcripts
 in the loci with more exons.

pinfish-dbgsym: debug symbols for pinfish
pinfish-examples: Examples and test data for pinfish

 The toolchain is composed of the following tools:
 1. spliced_bam2gff - a tool for converting sorted BAM
 files containing spliced alignments
 into GFF2 format. Each read will be represented as a distinct
 transcript. This tool comes handy when visualizing spliced
 reads at particular loci and to provide input to the rest
 of the toolchain.
 .
 2. cluster_gff - this tool takes a sorted GFF2 file as
 input and clusters together reads having similar
 exon/intron structure and creates a rough consensus
 of the clusters by taking the median of exon
 boundaries from all transcripts in the cluster.
 .
 3. polish_clusters - this tool takes the cluster
 definitions generated by cluster_gff and for each
 cluster creates an error corrected read by mapping
 all reads on the read with the median length
 and polishing it using racon. The polished reads
 can be mapped to the genome using minimap2 or GMAP.
 .
 4. collapse_partials - this tool takes GFFs generated
 by either cluster_gff or polish_clusters and filters
 out transcripts which are likely to be based on RNA
 degradation products from the 5' end. The tool clusters
 the input transcripts into "loci" by the 3' ends and
 discards transcripts which have a compatible transcripts
 in the loci with more exons.
 .
 This package contains a test data set as well as sample scripts
 running some test suite provided by Debian also as autopkgtest.