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  1. DRIVE Breast Cancer OncoArray Genotypes dbGaP

    ID: phs001265.v1.p1

    Description: Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) was one of five projects funded in 2010 as part of the NCI's Genetic A...

  2. Genome Variations Among the Aboriginals in Malaysia dbGaP

    ID: phs000664.v1.p1

    Description: Copy number variation (CNV) has been recognized as a major contributor to human genome diversity. It plays an important role in determining phenotypes...

    Study Types: Population

  3. Comparison of custom capture for targeted next generation DNA sequencing dbGaP

    ID: phs000811.v1.p1

    Description: Targeted, capture-based DNA sequencing is an economical way to sequence a customized region of the genome. Several targeted sequencing kits are availa...

  4. HeLa Cell Genome Sequencing Studies dbGaP

    ID: phs000640.v3.p1

    Description: This study contains all authorized whole genome sequence data of the HeLa cell line from datasets currently in dbGaP. These data have been approved fo...

    Study Types: Whole Genome Sequencing

  5. Comparative Analysis of Primary and Metastatic Colorectal Cancer dbGaP

    ID: phs000790.v1.p1

    Description: Molecular profiling for somatic mutations that predict response to anti-EGFR therapy in colorectal cancer (CRC) has become standard practice. However,...

    Study Types: Cohort


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