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  1. LungCT-Diagnosis TCIA

    ID: LungCT-Diagnosis

    Date Released: 12-30-2014

  2. Soft-tissue-Sarcoma TCIA

    ID: Soft-tissue-Sarcoma

    Date Released: 06-01-2015

  3. TCGA-THCA TCIA

    ID: TCGA-THCA

    Date Released: 12-31-2014

  4. PROSTATEx TCIA

    ID: PROSTATEx

    Date Released: 03-30-2017

  5. TCGA-BLCA TCIA

    ID: TCGA-BLCA

    Date Released: 01-30-2017

  6. TCGA-SARC TCIA

    ID: TCGA-SARC

    Date Released: 12-30-2014

  7. TCGA-COAD TCIA

    ID: TCGA-COAD

    Date Released: 10-14-2014

  8. TCGA-LUAD TCIA

    ID: TCGA-LUAD

    Date Released: 01-30-2017

  9. RIDER Breast MRI TCIA

    ID: RIDER Breast MRI

    Date Released: 11-08-2011

  10. TCGA-ESCA TCIA

    ID: TCGA-ESCA

    Date Released: 12-09-2014

  11. TCGA-KICH TCIA

    ID: TCGA-KICH

    Date Released: 05-21-2014

  12. CBIS-DDSM TCIA

    ID: CBIS-DDSM

    Date Released: 08-31-2016

  13. TCGA-UCEC TCIA

    ID: TCGA-UCEC

    Date Released: 04-29-2015

  14. Phantom FDA TCIA

    ID: Phantom FDA

    Date Released: 08-04-2014

  15. QIN GBM DCE-MRI TCIA

    ID: QIN GBM DCE-MRI

    Date Released: 08-14-2015

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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


Displaying 20 of 79,251 results for " "