bcftools merge changing the alleles

Open
#726 2 comments 0 reactions 0 assignees View on GitHub

Nobody has claimed this yet.

Assessment

Difficulty
4/5
Estimated time
3-5 days
Newbie friendliness
25/100
Issue type
Bug
Clarity
Needs clarification
Activity status
Stale
Tech stack
c

Research direction

Start by reproducing the reported bcftools merge -m id command with file1.vcf.gz and file2.vcf.gz, comparing the input and output allele strings. Trace the merge path responsible for allele handling and add a regression test using the reported multi-allelic marker; done means merging preserves the complete allele sequences.

Written by the indexing model from the issue text.

Description

enhancement

Command:
bcftools merge -m id file1.vcf.gz file2.vcf.gz -O z -o output.vcf.gz

For one of the multi-allelic markers, alleles in file1 and file2:
CGAATGGAATGGAATGGAAT CGAATGGAATGGAAT,CAAATGGAATGGAATGGAAT,CGAATGGAATCGAATGGAAT,CGAATGGAATTGAATGGAAT

Alleles in output:
CGAATGGAATG CGAATG,CAAATGGAATG,CGAATGGAATC,CGAATGGAATT
(i.e. it is stripping down the alleles)

File1 and file 2 do not have overlapping samples. Any help with this?

Dominant language
C
Stars
891
Forks
277
Avg merge
2d 23h
Merged PRs (30d)
2

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.

More from samtools/bcftools

All issues in samtools/bcftools

Similar issues

More C issues

Get new issues in your inbox

A short digest of beginner-friendly GitHub issues.