Heterozygous sites across genome

sanger-tol / variantcalling

This Nextflow DSL2 pipeline calls variants on long read alignment. It is run after sanger-tol/readmapping in the Sanger ToL production suite but with options to run on unaligned reads.

https://pipelines.tol.sanger.ac.uk/variantcalling

MIT License

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Heterozygous sites across genome #42

Open priyanka-surana opened 1 year ago

priyanka-surana commented 1 year ago

Description of feature

Create bedGraph for distribution of heterozygous sites across genome

gq1 commented 7 months ago

Hi @priyanka-surana can you give more details for this issue? thanks.