calkan / TARDIS-BAM-NextFlow

Tool for automated and rapid discovery of structural variants

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Tardis

Nextflow wrapper script for BilkentCompGen/tardis, runs TARDIS in QUICK MODE. See original documentation for more details.

Example Command

nextflow run lifebit-ai/Tardis
--input_folder s3://1000genomes/phase3/data/NA12878/high_coverage_alignment/NA12878.mapped.ILLUMINA.bwa.CEU.high_coverage_pcr_free.20130906.bam
--ref s3://lifebit-featured-datasets/pipelines/tardis-data/human_g1k_v37.fasta
--sonic s3://lifebit-featured-datasets/pipelines/tardis-data/human_g1k_v37.sonic
--bam_file_prefix NA12878.mapped.ILLUMINA.bwa.CEU.high_coverage_pcr_free.20130906

bam_file_prefix is an optional argument to run TARDIS only on one BAM file if multiple BAMs are present in input_folder. All other arguments are mandatory.

Running on Deploit

Example can be seen by selecting "Try with example data & parameters". Substitute input_folder for your own folder containing BAM files. If the BAM was aligned against a different reference genome ref and sonic parameters will also need to be changed. Sonic files for different reference genomes can be downloaded from here or you can make your own. Screen Shot 2018-11-08 at 10.36.22.png

Output

Output vcf files use the name of the input BAM file(s). Example output: Screen Shot 2018-11-08 at 10.32.58.png

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Tool for automated and rapid discovery of structural variants


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