URL: https://github.com/nf-core/variantbenchmarking
Proper Citation: variantbenchmarking (RRID:SCR_028995)
Description: Software pipeline to evaluate and validate the accuracy of variant calling methods in genomic research. The workflow provides benchmarking tools for small variants including SNVs and INDELs, Structural Variants (SVs) and Copy Number Variations (CNVs) for germline and somatic analysis.
Synonyms: nf-core-variantbenchmarking
Resource Type: software resource, software toolkit, source code
Keywords: evaluate and validate accuracy of variant calling methods, genomic research, variant calling, germline and somatic analysis,
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