Genomic variants - SNPs and INDELs detection using SAMTools. Version 1
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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.
Inputs
| ID | Name | Description | Type |
|---|---|---|---|
| sars_cov_2_reference_genome | n/a | n/a | File |
| rnaseq_left_reads | n/a | n/a | File |
| rnaseq_right_reads | n/a | n/a | File |
| sample_name | n/a | n/a | string |
Steps
| ID | Name | Description |
|---|---|---|
| index_reference_genome_with_bowtie2 | ||
| align_rnaseq_reads_to_genome | ||
| index_reference_genome_with_samtools | ||
| sam_to_bam_conversion_using_samtools_view | ||
| sort_alignment_files_using_samtools_sort | ||
| index_bam_files_using_samtools_index | ||
| snp_generation_using_bcftools | ||
| indel_generation_using_bcftools |
Outputs
| ID | Name | Description | Type |
|---|---|---|---|
| snp | n/a | n/a | File |
| indel | n/a | n/a | File |
Creators and Submitter
Views: 847 Downloads: 68
Created: 17th Jun 2020 at 08:41
Last updated: 27th Jun 2020 at 02:27
Last used: 6th Dec 2021 at 13:04
AttributionsNone
Version History
Version 1 Created 17th Jun 2020 at 08:41 by Ambarish Kumar
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