Research Object Crate for Genomic variants - SNPs and INDELs detection using VARSCAN2.

Original URL: https://workflowhub.eu/workflows/31/ro_crate?version=1

Author: AMBARISH KUMAR er.ambarish@gmail.com; ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using VARSCAN. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence.

Author: Ambarish Kumar
License: Apache-2.0

Main Workflow: Genomic variants - SNPs and INDELs detection using VARSCAN2.
Size: 2917 bytes

Main Workflow Diagram: graph1.png
Size: 57754 bytes

Research Object Crate for Genomic variants - SNPs and INDELs detection using VARSCAN2.

Contents