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URL: https://software.broadinstitute.org/cancer/cga/polysolver
Proper Citation: Polysolver (RRID:SCR_022278)
Description: Software tool for HLA typing based on whole exome sequencing data and infers alleles for three major MHC class I genes. Enables accurate inference of germline alleles of class I HLA-A, B and C genes and subsequent detection of mutations in these genes using inferred alleles as reference.
Synonyms: POLYmorphic loci reSOLVER, POLYSOLVER
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: PMID:26372948
Keywords: HLA typing, whole exome sequencing data, accurate inference of germline alleles, high precision HLA-typing, alleles of class I HLA-A, B and C genes, detection of mutations, inferred alleles
Funding: AACR ; Blavatnik Family Foundation ; NCI 1R01CA155010; NHLBI 1RO1HL103532
Availability: Free, Available for download, Freely available
Resource Name: Polysolver
Resource ID: SCR_022278
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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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