Add to schema all items from rnaseq
Open
Nobody has claimed this yet.
enhancement
- Dominant language
- Nextflow
- Stars
- 23
- Forks
- 6
- Avg merge
- 1d 9h
- Merged PRs (30d)
- 6
Description
- additional_fasta
- bbsplit_index | bbsplit
- fasta
- gene_bed | bed12
- gff
- gtf
- hisat2_index | hisat2
- kallisto_index | kallisto
- rsem_index | rsem
- salmon_index | salmon
- sortmerna_index | sortmerna
- star_index | star
- transcript_fasta
Contributor guide
First steps
- Read the whole issue, then the project's contributing guide.
- Comment on the issue to say you are picking it up — it saves two people doing the same work.
- Fork the repository and make your change on a branch.
- Open a pull request that references the issue number.
Research direction
Start by locating the schema and the rnaseq definitions in the repository, then compare the checklist with the existing entries. Done means the missing items—additional_fasta, bbsplit_index, gene_bed, and sortmerna_index—are represented in the schema alongside the entries already marked complete.
Written by the indexing model from the issue text.
Assessment
- Domain
- bioinformatics
- Issue type
- Feature
- Difficulty
- 3/5
- Estimated time
- 1-2 days
- Activity status
- Stale
- Clarity
- Mostly clear
- Newbie friendliness
- 38/100