URL: https://imputation.biodatacatalyst.nhlbi.nih.gov/#!
Proper Citation: TOPMed Imputation Server (RRID:SCR_028178)
Description: Free, secure cloud-based service used to impute missing genetic variants in human DNA data, primarily for genome-wide association studies (GWAS). It uses a massive, diverse reference panel of deeply sequenced human genomes to predict missing genotypes, significantly increasing genetic coverage and improving accuracy, particularly for rare variants. It leverages the Trans-Omics for Precision Medicine (TOPMed) panel, which includes over 400 million variants, allowing researchers to boost their genomic data from millions of SNPs to tens of millions.
Synonyms: , NHLBI TOPMed Imputation Server, Trans-Omics for Precision Medicine Imputation Server
Resource Type: data access protocol, software resource, web service
Defining Citation: PMID:33568819
Keywords: impute missing genetic variants in human DNA data, genome-wide association studies, missing genetic variants, human DNA data,
Availability: Restricted
Resource Name: TOPMed Imputation Server
Resource ID: SCR_028178
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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
