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URL: https://pathoman.mskcc.org/
Proper Citation: PathoMAN (RRID:SCR_026552)
Description: Web application to automate germline genomic variant curation from clinical sequencing based on ACMG guidelines. Aggregates multiple tracks of genomic, protein and disease specific information from public sources.
Abbreviations: PathoMAN
Synonyms: Pathogenicity of Mutation Analyzer
Resource Type: software resource, web application
Defining Citation: PMID:30787465
Keywords: Aggregates multiple tracks, automate germline genomic variant curation, clinical sequencing, genomic, protein, disease specific information, public sources,
Funding: NCI P30CA008748; NCI P50CA221745; NCI R21CA029533
Availability: Free, Freely available,
Resource Name: PathoMAN
Resource ID: SCR_026552
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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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