Variant annotation and filtration server ALAPY Genome Explorer
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Updated
May 22, 2017 - Shell
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Variant annotation and filtration server ALAPY Genome Explorer
Merge in parallel, speeding up bcftools merge
This is a shell-scripted bioinformatics pipeline to process NGS data into interpretable mutation and somatic variant calls and finally visualising them in IGV. It integrates industry-standard tools and supports automated execution.
A bash script that synchronizes and processes vCard (.vcf) files between directories while adding visual lock indicators to contact names to imply a file is read-only.
Modify KASP assay calls to a VCF format
Add a description, image, and links to the vcf-files topic page so that developers can more easily learn about it.
To associate your repository with the vcf-files topic, visit your repo's landing page and select "manage topics."