nf-core / nf-core/references

Add tools from rnaseq

Open
#16 0 comments 0 reactions 0 assignees View on GitHub

Nobody has claimed this yet.

enhancement
Dominant language
Nextflow
Stars
23
Forks
6
Avg merge
1d 9h
Merged PRs (30d)
6

Description

nf-core modules

  • bbmap/bbsplit
  • custom/catadditionalfasta
  • custom/getchromsizes
  • gffread
  • hisat2/build
  • hisat2/extractsplicesites
  • kallisto/index
  • rsem/preparereference
  • salmon/index
  • sortmerna
  • star/genomegenerate

local modules

  • gtf2bed
  • gtf_filter
  • preprocess_transcripts_fasta_gencode

Contributor guide

Open the contributing guide

First steps

  1. Read the whole issue, then the project's contributing guide.
  2. Comment on the issue to say you are picking it up — it saves two people doing the same work.
  3. Fork the repository and make your change on a branch.
  4. Open a pull request that references the issue number.

Research direction

Start by examining the completed nf-core entries such as gffread, hisat2/build, kallisto/index, and star/genomegenerate, then compare them with the unchecked nf-core and local module names. Add the remaining listed tools, including bbmap/bbsplit, sortmerna, gtf2bed, gtf_filter, and preprocess_transcripts_fasta_gencode. Done means the unchecked entries are implemented consistently with the existing modules.

Written by the indexing model from the issue text.

Assessment

Domain
bioinformatics
Issue type
Feature
Difficulty
4/5
Estimated time
3-5 days
Activity status
Stale
Clarity
Mostly clear
Newbie friendliness
35/100

Get new issues in your inbox

A short digest of beginner-friendly GitHub issues.