Workflow Steps and Code Snippets
3191 tagged steps and code snippets that match keyword SAMtools
Snakemake workflow: dna-seq-gatk-variant-calling (v2.1.1)
38 39 | shell: "samtools dict {input} > {output} 2> {log} " |
Snakemake workflow: dna-seq-gatk-variant-calling (v2.1.1)
38 39 | shell: "samtools dict {input} > {output} 2> {log} " |
Snakemake workflow: dna-seq-gatk-variant-calling (v2.1.1)
38 39 | shell: "samtools dict {input} > {output} 2> {log} " |
Snakemake workflow: dna-seq-gatk-variant-calling (v2.1.1)
38 39 | shell: "samtools dict {input} > {output} 2> {log} " |
WES analysis pipeline
50 51 52 53 54 55 56 57 58 | shell: """ gatk SamToFastq -I {input.bam} -F /dev/stdout -INTER true -NON_PF true \ | \ bwa mem -p -v 3 -t {threads} -T 0 \ {input.ref} /dev/stdin - 2> >(tee {log} >&2) \ | \ samtools view -Shb -o {output} """ |
166 167 168 169 | shell: """ samtools flagstat {input} > {output} """ |
Snakemake pipeline for detection limit test from laser-microdissected samples
59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 | shell: """ if [[ {params.is_paired} = "True" ]] ; then (bowtie2 \ -x {input.mock} \ -1 {input.forward_} \ -2 {input.reverse_} \ --threads {threads} \ --rg-id '{params.rg_id}' \ --rg '{params.rg_extra}' \ {params.extra} \ | samtools sort \ --threads {threads} \ -m {params.samtools_mem} \ | samtools rmdup - - \ | samtools view \ --reference {input.reference} \ --output {output.cram} \ --output-fmt cram,level=9,nthreads={threads} \ --write-index \ ) 2> {log} 1>&2 else (bowtie2 \ -x {input.mock} \ -U {input.forward_} \ --threads {threads} \ --rg-id '{params.rg_id}' \ --rg '{params.rg_extra}' \ {params.extra} \ | samtools sort \ --threads {threads} \ -m {params.samtools_mem} \ | samtools rmdup -s - - \ | samtools view \ --reference {input.reference} \ --output {output.cram} \ --output-fmt cram,level=9,nthreads={threads} \ --write-index \ ) 2> {log} 1>&2 fi """ |
123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 | shell: """ if [[ {params.is_paired} = "True" ]] ; then (samtools view \ --reference {input.reference} \ --threads {threads} \ -u \ -o /dev/stdout \ -f 12 \ {input.cram} \ | samtools fastq \ -1 {output.forward_} \ -2 {output.reverse_} \ -0 /dev/null \ -c 9 \ --threads {threads} \ ) 2> {log} 1>&2 else (samtools view \ --reference {input.reference} \ --threads {threads} \ -u \ -o /dev/stdout \ -f 4 \ {input.cram} \ | samtools fastq \ -0 {output.forward_} \ -c 9 \ --threads {threads} \ ) 2> {log} 1>&2 fi """ |
59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 | shell: """ if [[ {params.is_paired} == "True" ]] ; then (bowtie2 \ -x {input.mock} \ -1 {input.forward_} \ -2 {input.reverse_} \ --threads {threads} \ --rg-id '{params.rg_id}' \ --rg '{params.rg_extra}' \ {params.extra} \ | samtools sort \ -l 9 \ -M \ -m {params.samtools_mem} \ -o {output.cram} \ --reference {input.reference} \ --threads {threads} \ --write-index \ ) 2> {log} 1>&2 else (bowtie2 \ -x {input.mock} \ -U {input.forward_} \ --threads {threads} \ --rg-id '{params.rg_id}' \ --rg '{params.rg_extra}' \ {params.extra} \ | samtools sort \ -l 9 \ -M \ -m {params.samtools_mem} \ -o {output.cram} \ --reference {input.reference} \ --threads {threads} \ --write-index \ ) 2> {log} 1>&2 fi """ |
12 13 | shell: "samtools flagstats {input.cram} > {output.txt} 2> {log}" |
tool / biotools
SAMtools
SAMtools and BCFtools are widely used programs for processing and analysing high-throughput sequencing data. They include tools for file format conversion and manipulation, sorting, querying, statistics, variant calling, and effect analysis amongst other methods.