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Displaying 20 of 79,180 results for " "
  1. NCI Cancer Genome Characterization Initiative (CGCI) dbGaP

    ID: phs000235.v3.p1

    Description: The Office of Cancer Genomics at the National Cancer Institute is sponsoring a series of studies as part of the Cancer Genome Characterization Initia...

    Study Types: Tumor vs. Matched-Normal

  2. Alcohol Research using Australian twins and their families (OZ-ALC) dbGaP

    ID: phs000181.v1.p1

    Description: The Australian twin-family study of alcohol use disorder (OZALC study) derives from telephone diagnostic interview studies of two general population v...

  3. Applying Genomic Sequencing in Pediatrics (PediSeq) dbGaP

    ID: phs000935.v1.p1

    Description: The purpose of this research study is to learn more about newer types of genetic testing called whole exome sequencing and whole genome sequencing. Cu...

  4. CGEMS Breast Cancer GWAS dbGaP

    ID: phs000147.v2.p1

    Description: The initial stage of the Cancer Genetic Markers of Susceptibility (CGEMS) breast cancer genome-wide association study (GWAS) included genotyping 528,1...

    Study Types: Case-Control

  5. DNA Methylation Analysis of Prostate Cancer dbGaP

    ID: phs000597.v1.p1

    Description: Aberrant DNA methylation changes are known to occur during prostate cancer progression beginning with precursor lesions. Utilizing fifty nanograms of ...

    Study Types: Case-Control

  6. Single Cell Analysis Program - Transcriptome (SCAP-T) dbGaP

    ID: phs000833.v4.p1

    Description: This initiative is part of the Single Cell Analysis Program (SCAP) and is funded through the NIH Common Fund (See, which s...

    Study Types: Single Cell Analysis

  7. NINDS Stroke Genetics Network (SiGN) dbGaP

    ID: phs000615.v1.p1

    Description: The NINDS Stroke Genetics Network (SiGN) is a large international collaboration designed to detect genetic variants that predispose to subtypes of isc...

    Study Types: Case-Control

  8. NHLBI Exome Sequencing in SCID dbGaP

    ID: phs000479.v1.p1

    Description: Analysis of the molecular etiologies of severe combined immunodeficiency (SCID) has led to important insights into the control of immune cell developm...

    Study Types: Parent-Offspring Trios

  9. NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (SWISS) dbGaP

    ID: phs000327.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...

  10. PGRN-RIKEN MA.27 Mayo Aromatase Inhibitor Musculoskeletal Adverse Events Study dbGaP

    ID: phs000210.v1.p1

    Description: Source of Patients The source of the patients for this genome-wide case control study was MA.27, which was conducted as a multi-cooperative group ef...

    Study Types: Nested Case-Control

  11. Study of Melanoma Risk in Australia and the United Kingdom dbGaP

    ID: phs000519.v1.p1

    Description: The results from a small number of melanoma GWAS have been published. Initial studies identified several pigmentation- and nevus-associated loci that ...

    Study Types: Case Set

  12. SLCO1B1 Variants and Methotrexate Clearance dbGaP

    ID: phs000426.v1.p1

    Description: Methotrexate plasma concentration is related to its clinical effects. To identify the genetic basis of interindividual variability in methotrexate...

    Study Types: Cohort

  13. Study of Irish Amyotrophic Lateral Sclerosis (SIALS) dbGaP

    ID: phs000127.v2.p1

    Description: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by loss of motor neurons. Epidemiological studies indicate...

    Study Types: Case-Control

  14. A Prognostic Role of APC in Colorectal Cancers dbGaP

    ID: phs001111.v1.p1

    Description: Colorectal cancer (CRC) is a highly heterogeneous disease, for which prognosis has been relegated to clinic-pathologic staging for decades. There is a...

    Study Types: Case Set

  15. Genetics Consortium for Late Onset of Alzheimer's Disease (LOAD CIDR Project) dbGaP

    ID: phs000160.v1.p1

    Description: Multiplex Family StudyThe purpose of the NIA Genetics Initiative: Multiplex Family Study is to identify families with multiple members diagnosed wit...

  16. Functionally Active Copy Number Variants Associated with Prostate Cancer Risk dbGaP

    ID: phs000487.v2.p1

    Description: Prostate cancer is a leading cause of cancer death in males throughout the world and has the largest estimated effect of heritability among the most c...

    Study Types: Case-Control

  17. Exome Sequencing of Pleuropulmonary Blastoma dbGaP

    ID: phs000543.v1.p1

    Description: Pleuropulmonary blastoma (PPB) is a rare, aggressive pediatric cancer arising from the lung or pleural cavity. In this study, we sequenced and analyze...

  18. NHLBI TOPMed: Genes-environments and Admixture in Latino Asthmatics (GALA II) Study dbGaP

    ID: phs000920.v1.p1

    Description: This is a case-only pharmacogenetic study of bronchodilator drug response among racially admixed Latino children with asthma. The overall goal is to i...

    Study Types: Case Set

  19. NHLBI and NIA The New England Centenarian Study (NECS) dbGaP

    ID: phs000451.v1.p1

    Description: Supercentenarians (age 110+ years old) generally delay or escape age-related diseases and disability well beyond the age one hundred and this exceptio...

    Study Types: Case Set

  20. A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD) dbGaP

    ID: phs000421.v1.p1

    Description: Fuchs' Endothelial Corneal Dystrophy (FECD) is a common disease that results in loss of vision associated with progressive corneal edema and loss ...

Displaying 20 of 79,180 results for " "