Investigate VDS format for the creation of a false positive variants list

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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Investigate VDS format for the creation of a false positive variants list #65

Open nvnieuwk opened 9 months ago

nvnieuwk commented 9 months ago

Description of feature

https://hail.is/docs/0.2/vds/index.html