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URL: https://github.com/bioinform/somaticseq
Proper Citation: SomaticSeq (RRID:SCR_024891)
Description: Software accurate somatic mutation detection pipeline implementing stochastic boosting algorithm to produce somatic mutation calls for both single nucleotide variants and small insertions and deletions. NGS variant calling and classification.
Resource Type: software resource, software toolkit
Defining Citation: PMID:26381235
Keywords: NGS variant calling and classification, somatic mutation detection, somatic mutation calls, single nucleotide variants, detect somatic mutations,
Funding: NHGRI R01 HG007834; NIGMS R01 GM109836
Resource Name: SomaticSeq
Resource ID: SCR_024891
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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
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