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

Original URL: https://workflowhub.eu/workflows/34/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 SAMTools. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence.

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License: Apache-2.0

Main Workflow: Genomic variants - SNPs and INDELs detection using SAMTools.
Size: 2761 bytes

Main Workflow Diagram: graph3.png
Size: 54065 bytes

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

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