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Claim

sv-callers workflow

Abstract

sv-callers is a Snakemake-based workflow that combines several state-of-the-art tools for detecting structural variants (SVs) in whole genome sequencing data. This workflow is easy to use and to deploy on any Linux-based machine. In particular, the workflow supports automated software deployment, easy configuration and addition of new analysis tools as well as enables to scale from a single computer to different HPC clusters with minimal effort. The workflow includes the following SV callers Manta DELLY LUMPY GRIDSS and post-processing tools BCFtools Viola-SV SURVIVOR

Related Organizations
Keywords

cancer genomics, whole genome sequencing, BAM, somatic variants, variant calling, workflow, VCF, germline variants, HPC, structural variants, high-performance computing, bioinformatics, WGS

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
OpenAIRE UsageCountsViews provided by UsageCounts
downloads
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2
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48
6
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Cancer Research