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The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the data and results from studies that have investigated the interaction of genotype and phenotype in Humans.
Genetic Relationship and Fingerprinting (GRAF) is a rapid statistical method to detect duplicates and closely related samples in large genomic datasets to be used as a quality assurance tool in dbGaP data processing. For more information, see this abstract in PubMed.
https://www.ncbi.nlm.nih.gov/pubmed/28609482
An integrated application for viewing and analyzing sequence data. With Genome Workbench, you can view data in publically available sequence databases at NCBI, and mix these data with your own data.
Provides an overview of the C++ language with a focus on its use in accessing resources of the National Center for Biotechnology Information at the National Library of Medicine, National Institutes of Health.
A public domain quality assurance software package that facilitates the assessment of multiplex short tandem repeat (STR) DNA profiles based on laboratory-specific protocols.
RxNav-in-a-Box provides users with a locally-installable RxNav (https://rxnav.nlm.nih.gov/RxNavDoc.html) and RESTful companion APIs, including RxNorm, RxTerms, RxClass, RxCUI history, and drug-drug interactions.