Genomic variants - SNPs and INDELs detection using GATK4.
Version 1

Workflow Type: Common Workflow Language
Stable

Author: AMBARISH KUMAR er.ambarish@gmail.com & ambari73_sit@jnu.ac.in

This is a proposed standard operating procedure for genomic variant detection using GATK4.

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
indices_folder n/a n/a
  • Directory

Steps

ID Name Description
index_reference_genome_with_bowtie2 n/a n/a
align_rnaseq_reads_to_genome n/a n/a
index_reference_genome_with_samtools n/a n/a
create_sequence_dictionary n/a n/a
update_read_group n/a n/a
mark_duplicates n/a n/a
split_alignments n/a n/a
index_split_alignments n/a n/a
call_plausible_haplotypes_and_detect_variants n/a n/a
filer_out_low_quality_variants n/a n/a
select_indels n/a n/a
select_snps n/a n/a

Outputs

ID Name Description Type
indels n/a n/a
  • File
snps n/a n/a
  • File

Version History

Version 1 (earliest) Created 17th Jun 2020 at 07:11 by Ambarish Kumar

Added/updated 2 files


Open master f0602cf
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Views: 1438   Downloads: 55

Created: 17th Jun 2020 at 07:11

Last used: 2nd Dec 2022 at 06:21

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