nf-cmgg / structural

A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
https://nf-cmgg.github.io/structural/
MIT License
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smoove.vcf.gz indexin #86

Closed mvheetve closed 4 months ago

mvheetve commented 4 months ago

Description of the bug

When using --output_callers, the directory containing

- smoove.vcf.gz
- svync.smoove.vcf.gz.tbi 

smoove.vcf.gz should be indexed when created and svync.smoove.vcf.gz.tbi can go.

Command used and terminal output

No response

Relevant files

No response

System information

No response

nvnieuwk commented 4 months ago

This has been fixed in #89