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Assessment of epigenetic variation in human iPS cells-Medip
Dataset
EGAD00001000827
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Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects.
Dataset
EGAD00001004124
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Sequencing component for the whole genome methylation analysis in PBMCs and cell subsets (pilot study)
Dataset
EGAD00001000394
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How upcycled prostate cancer sequences enabled key findings on telomeres length
Blog
prostate-cancer-sequences-enabled-key-findings-on-telomeres-length
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Tumor-specific expression of let-7i and miR-192 is associated with resistance to cisplatin-based chemoradiotherapy in patients with larynx and hypopharynx cancer
Study
EGAS00001004001
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Cystic Fibrosis Nasal Epithelium Gene Expression by RNAseq
Study
phs002254
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Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
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MP2PRT: Evaluation of an Inflammation Polygenic Risk Score (iPRS) to Predict Cancer Related Cognitive Impairment and Fatigue in Patients Receiving Chemotherapy for Non-Metastatic Breast Cancer in URCC0701 and URCC10055
Study
phs003688
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GA4GH
Documentation
about/projects-and-funders/ga4gh
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This committee is composed on individuals who have access to the data corresponding to this project:
Gut microbiome modulates response to anti PD-1 immunotherapy in melanoma patients
Dac
EGAC00001000758
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Dental Caries: Whole Genome Association and Gene x Environment Studies
Study
phs000095
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Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
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Unrelated Donor Reduced Intensity Bone Marrow Transplant for Children with Severe Sickle Cell Disease (BMT CTN-0601-BioLINCC)
Study
phs003470
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Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array
Study
EGAS00000000105
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Evaluating potential drug candidates for the treament of Henamgiopericytoma on patient derived cell line models
Study
EGAS50000000027
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RNAseq and ATACseq on HGSC lines, pre- and post-treatment with an epigenetic drug
Study
EGAS50000000047
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NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF)
Study
phs001032
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Genetic Susceptibility and Biomarkers of Platinum-Related Toxicities
Study
phs001621
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Washington University Coronary Artery Disease Study
Study
phs001227
-
Family-Based Study on Ulcerative Colitis with Whole Exome Sequencing
Study
phs001251
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Determinants of Asthma Following RSV Bronchiolitis in Early Life
Study
phs001009
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RareBliss: Rare Bipolar Loci Identification Through Sequencing Study
Study
phs001358
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Rapid Acceleration of Diagnostics - Digital Health Technologies' (RADx-DHT) Collection of General Research Use Datasets
Study
phs003666
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Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Dataset
EGAD00001009740
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WES of pleomorphic lung cancer
Dataset
EGAD50000000453
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Whole exome sequencing data of patients with resectable esophageal adenocarcinoma treated with neoadjuvant atezolizumab and chemoradiation (PERFECT)
Study
EGAS00001006504
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Clonal Evolution of PPM1D Mutations in the Spectrum of Myeloid Disorders
Study
EGAS50000000840
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Personalized Treatment of Sezary Syndrome through a CTLA4:CD28 Fusion
Study
phs000773
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DFCI Gynecological Oncology Data Access Committee
Dac
EGAC50000000712
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Whole genome sequence: cardiomyopathy, 1 myotonic dystrophy patient
Study
JGAS000706
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Paraganglioma Smart-Seq2 Single Nuclei Sequencing Data
Study
EGAS50000001184
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HNF1B induced three-dimentional genome analysis of patient-derived pancreas neoplasm organoids
Study
JGAS000514
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Gene expression analysis for nasal polyps
Study
JGAS000153
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Comprehensive genomic analysis of patient derived orthotopic xenograft model in primary central nervous system lymphoma
Study
JGAS000178
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The prevalence and clinical characteristics of TECTA-associated autosomal dominant hearing loss.
Study
JGAS000201
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Transcriptome analysis of adolescents and young adults with Acute Lymphoblastic Leukemia
Study
JGAS000047
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Identification of genetic mutations characteristic for recurrence and metastasis of colon and rectal cancer.
Study
JGAS000091
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Genomic Data from Patients with Advanced Rare Cancers Treated with Pembrolizumab
Study
EGAS50000001508
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Transcriptomic Data from Patients with Advanced Rare Cancers Treated with Pembrolizumab
Study
EGAS50000001509
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scRNA transcriptome and TCR sequencing data modeling treatment responses in eight renal cell carcinoma patient
Dataset
EGAD50000001934
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Genomic evolution of pancreatic cancer at single-cell resolution
Study
EGAS50000001351
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Multi-modal single-cell analysis of salivary glands from patients with Sjogren's syndrome
Study
JGAS000808
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The_evolution_of_CML
Study
EGAS00001005095
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Diseased_heart_analysis__RNA_Adult
Study
EGAS00001008302
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Whole exome sequencing from early stage non-small cell lung cancer patients at MDACC
Study
EGAS00001004026
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Abnormal_foetal_development_exome_trios
Study
EGAS00001000167
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TTV018_RORC_IBD_associated_genotype_effects_on_RORgT_expression_and_function_in_ex_vivo_T_cells
Study
EGAS00001001590
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Y_phylogeny_haplogroupDE
Study
EGAS00001002674
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Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Study
EGAS00001000712
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Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463