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,
Availability: Free, Available for download, Freely available
Resource Name: variantbenchmarking
Resource ID: SCR_028995
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
