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Displaying 20 of 79,180 results for " "
  1. International Standards for Cytogenomic Arrays dbGaP

    ID: phs000205.v6.p2

    Description: The International Standards for Cytogenomic Arrays (ISCA) Consortium is a rapidly growing group of clinical cytogenetics and molecular genetics labora...

    Study Types: Clinical Genetic Testing

  2. Genome-Wide Association Analysis of Serum Iron in the InCHIANTI and BLSA dbGaP

    ID: phs000215.v1.p1

    Description: The aim of this study was to identify gene(s) associated with serum iron concentrations. This dataset contains the results from a meta-analysis of 1...

  3. NHGRI Tumor Sequencing Project (Lung Adenocarcinoma) dbGaP

    ID: phs000144.v1.p1

    Description: The Tumor Sequencing Project (TSP) Consortium is a collaboration among participants at the Baylor College of Medicine Human Genome Sequencing Center...

    Study Types: Tumor vs. Matched-Normal

  4. Chromothripsis in Patient WHIM-09 dbGaP

    ID: phs000856.v1.p1

    Description: We are studying the natural history, pathogenesis and treatment of patients with WHIM syndrome, an immunodeficiency disorder characterized by warts, h...

    Study Types: Single Patient

  5. Alzheimer's Disease Sequencing Project (ADSP) dbGaP

    ID: phs000572.v3.p2

    Description: The overarching goals of the ADSP are to: (1) identify new genomic variants contributing to increased risk of developing AD, (2) identify new genomic ...

  6. Genetics of Human Developmental Brain Disorders dbGaP

    ID: phs000492.v1.p1

    Description: Developmental brain malformations are at the core of significant neurological diseases affecting many families in the United States and around the wor...

  7. Genomic Characterization of Pediatric Low-Grade Gliomas dbGaP

    ID: phs001054.v1.p1

    Description: Pediatric low-grade gliomas (PLGGs) are the most common pediatric brain-tumor, with more than ten histologic subtypes recognized by the World Health O...

    Study Types: Case Set

  8. NextGen/GENESiPS dbGaP

    ID: phs001139.v1.p1

    Description: Variability in induced pluripotent stem cell (iPSC) lines remains a roadblock for disease modeling and regenerative medicine. Through linear mixed mod...

    Study Types: Case-Control

  9. Genome-Wide Association Study of Anorexia Nervosa dbGaP

    ID: phs000679.v1.p1

    Description: Twin studies are consistent with substantial heritability in anorexia nervosa (AN), although detecting and confirming individual risk alleles has been...

    Study Types: Case-Control

  10. T1DGC: Genome-Wide Association Study in Type 1 Diabetes, 2008 dbGaP

    ID: phs000180.v2.p2

    Description: Cases with Type 1 Diabetes (T1D) in the UK, were part of the Wellcome Trust Case Control Consortium (WTCCC) - - that first rep...

    Study Types: Case Set

  11. Family Genomics of Bipolar Disorder dbGaP

    ID: phs000866.v1.p1

    Description: This study examined the segregation of variants with phenotype in pedigrees harboring bipolar disorder.

    Study Types: Family

  12. Genome-wide Analysis of Lymphoma dbGaP

    ID: phs000328.v1.p1

    Description: Diffuse Large B-cell Lymphoma (DLBCL) represents the most common form of B-cell non-Hodgkin Lymphoma (B-NHL), accounting for ~30% of the de-novo diag...

    Study Types: Tumor vs. Matched-Normal

  13. NINDS Parkinson's Disease dbGaP

    ID: phs000089.v3.p2

    Description: Epidemiological studies have estimated a cumulative prevalence of PD of greater than 1 per thousand. When prevalence is limited to senior population...

    Study Types: Case-Control

  14. Brain Metastases in Squamous Cell Lung Cancers dbGaP

    ID: phs000907.v1.p1

    Description: Putative oncogenic pathways in squamous cell lung cancer have been recently characterized, although their biologic repercussions in patients is largel...

    Study Types: Case Set

  15. CSER-MedSeq dbGaP

    ID: phs000958.v1.p1

    Description: Whole genome sequencing (WGS) and whole exome sequencing (WES) services are currently available to and being utilized by physicians and their patients...

    Study Types: Case-Control

  16. Cutaneous Microbiome in Psoriasis (HMP Demonstration Study) dbGaP

    ID: phs000251.v2.p2

    Description: Psoriasis, a highly prevalent disease of humans of unknown cause, is a chronic inflammatory disorder primarily involving skin, with distinctive clinic...

    Study Types: Case-Control

  17. Natural Variation in Fish Transcriptomes: Comparative Analysis of the Fathead Minnow (Pimephales promelas) and Zebrafish (Danio rerio) OmicsDI

    ID: E-GEOD-60202

    Date Released: 08-19-2015

    Description: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

  18. Dazl is required for TET-mediated reprogramming to a naïve pluripotent state (I) OmicsDI

    ID: E-GEOD-69055

    Date Released: 08-19-2015

    Description: Embryonic stem cell (ESC) cultures display a heterogeneous gene expression profile, ranging from a pristine naïve pluripotent state to a primed epibl...

  19. Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells [time-course microarray] OmicsDI

    ID: E-GEOD-69321

    Date Released: 08-19-2015

    Description: Transcription factor-mediated reprogramming is a powerful method to study cell fate changes. In this work, we demonstrate that the transcription facto...

  20. E. histolytica and E. invadens OmicsDI

    ID: E-GEOD-67232

    Date Released: 08-19-2015

    Description: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

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