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Displaying 20 of 54,582 results for " "
  1. Tyrosine Kinase Mutations in Endometrial Cancer dbGaP

    ID: phs000841.v1.p1

    Description: The purpose of the original study was to search for somatic mutations in the tyrosine kinome of serous and clear cell endometrial carcinomas (human). ...

    Study Types: Case Set

  2. Geisinger eMERGE - Abdominal Aortic Aneurysm Project (AAAP) dbGaP

    ID: phs000387.v1.p1

    Description: A large research cohort of Geisinger Abdominal Aortic Aneurysm (AAA) patients was created by enrolling and consenting patients of the Geisinger De...

    Study Types: Case Set

  3. The Placenta Harbors a Unique Microbiome dbGaP

    ID: phs000735.v1.p1

    Description: This study is to investigate placental microbiome through 16S rDNA-based and whole genome shotgun metagenomic sequencing. Identified taxa and their ge...

    Study Types: Case-Cohort

  4. Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing dbGaP

    ID: phs000823.v1.p1

    Description: Melanoma risk shows clear heritability, but the inherited genetic factors remain largely unknown. Rare high risk mutations in CDKN2A, CDK4, BAP1 and T...

    Study Types: Case Set

  5. Genome Wide Association for Asthma and Lung Function dbGaP

    ID: phs000355.v1.p1

    Description: The SNP Typing for Association with Multiple Phenotypes from Existing Epidemiologic (STAMPEED) asthma project includes subjects with asthma and c...

    Study Types: Case-Control

  6. NCI GWAS of Renal Cell Carcinoma in African Americans dbGaP

    ID: phs000863.v1.p1

    Description: The NCI GWAS of renal cell carcinoma (RCC) in African Americans was undertaken to provide insight into genetic loci affecting susceptibility to this m...

    Study Types: Case-Control

  7. Integrative Clinical Sequencing Analysis of Metastatic Castration Resistant Prostate Cancer Reveals a High Frequency of Clinical Actionability dbGaP

    ID: phs000915.v1.p1

    Description: Most prostate cancer deaths are caused by metastatic, castration resistant disease (mCRPC). To develop a precision medicine framework for mCRPC, we es...

  8. Framingham SHARe Social Network dbGaP

    ID: phs000153.v7.p6

    Description: Note: Data Use Restrictions: The data must only be used for genetic research projects solely in the area of health-related social-network research. ...

    Study Types: Longitudinal

  9. Characterization of Pancreatic Adenocarcinoma Patients Using NGS dbGaP

    ID: phs000550.v1.p1

    Description: In this study, we whole genome sequenced tumor/normal pairs from three pancreatic adenocarcinoma patients to separately characterize each patient with...

    Study Types: Case Set

  10. Pancreatic Cancer Cohort and Case-Control Consortium (PanScan) dbGaP

    ID: phs000206.v5.p3

    Description: Within the framework of the NCI-sponsored Cohort Consortium, investigators from 12 prospective epidemiologic cohorts formed the Pancreatic Cancer Coho...

  11. Gene Mutation and Rescue in Congenital Diaphragmatic Hernia dbGaP

    ID: phs000485.v1.p1

    Description: Congenital Diaphragmatic Hernia (CDH) is a common and life-threatening malformation. The most common phenotype is left-sided posterolateral (Bochdalek...

  12. Patient-Specific Factors Influence Somatic Variations in VHL Tumors dbGaP

    ID: phs001107.v1.p1

    Description: Patients affected with von Hippel-Lindau disease are at risk of developing multiple independent clear cell renal carcinomas. This study performed whol...

    Study Types: Tumor vs. Matched-Normal

  13. Whole-Genome and Exome Sequencing in Clear-Cell Renal Cell Carcinoma dbGaP

    ID: phs000491.v1.p1

    Description: Study to evaluate the molecular genetics of ccRCC through integrative analyses of tumors and tumorgrafts using multiple platforms in clinically annota...

    Study Types: Case Set

  14. The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) trial dbGaP

    ID: phs000343.v1.p1

    Description: The VISP trial (PI Jim Toole, M.D., Wake Forest University School of Medicine) was a multi-center, double-blind, randomized, controlled clinical tria...

  15. NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy) dbGaP

    ID: phs000581.v1.p1

    Description: The NHLBI "Grand Opportunity" Exome Sequencing Project (GO-ESP), a signature project of the NHLBI Recovery Act investment, was designed to identify ge...

    Study Types: Case Set

  16. 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...

  17. 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

  18. 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...

  19. 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

  20. 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

Displaying 20 of 54,582 results for " "