-
Cancer Research UK Manchester Institute/ Cancer Research UK National Biomarker Centre Data Access Committee
Dac
EGAC50000000795
-
Nivolumab and Tumor Infiltrating Lymphocytes (TIL) in Advanced Non-Small Cell Lung Cancer
Study
phs002486
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Study
EGAS00001003190
-
Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT-BioLINCC)
Study
phs003654
-
WES data of one tumor of B-cell lymphoma
Dataset
EGAD00001006060
-
Million Veteran Program (MVP) Summary Results from Non-Sensitive Omics Studies
Study
phs002453
-
Data access committee for study - The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program "CASCADE".
Dac
EGAC00001000574
-
Clinical cancer panel sequencing (UCSF500) analysis of TERT promoter duplication in GBM.
Dataset
EGAD00001009286
-
Study of Cutaneous Biology of Cutaneous T Cell Lymphoma
Study
phs002717
-
Summarized somatic variant calls from CMMRD-associated high-grade gliomas
Dataset
EGAD50000002180
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RNAseq sample
Dataset
EGAD00001005747
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
SDR-seq_06_BCL
Study
EGAS50000000374
-
Platelet_collagen_defect
Study
EGAS00001000105
-
Whole-exome sequencing of the transposition of the great arteries
Study
EGAS00001004175
-
the Yemeni-Somali 5 million SNP array dataset
Study
EGAS00001003425
-
MCO colorectal cancer genomics at UNSW
Study
EGAS00001003450
-
Small Intestine Adenocarcinoma Subtyping Data Access Committee
Dac
EGAC50000000663
-
Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis-associated Variants
Study
phs001306
-
CLDN14 mutation identifed from Japanese sensorineural hearing loss patient.
Study
JGAS000191
-
Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis
Study
phs001743
-
NCI's Collection of Datasets for Health, Medical, and Biomedical Research Purposes
Study
phs003044
-
Familial adult myoclonic epilepsy type 1 in Sri Lankan and Indian families
Dataset
EGAD00001005777
-
ITER-FIISC Data Access Committee
Dac
EGAC50000000180
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
Data Access Committee for the DNA sequencing data included in the study "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes”
Dac
EGAC00001003111
-
Tumor Profiler DAC
Dac
EGAC50000000199
-
ITER-FIISC Data Access Committee (FPF)
Dac
EGAC50000000473
-
GenomeEUtwin Data Access Committee
Dac
EGAC00000000007
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
Data Access Committee for Translational analyses from a phase II study of pembrolizumab and epigenetic modification with azacitidine in platinum-resistant epithelial ovarian cancer
Dac
EGAC50000000697
-
Beta-Blocker Evaluation in Survival Trial (BEST-BioLINCC)
Study
phs003730
-
Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED-BioLINCC)
Study
phs004020
-
Transcriptome and epigenomic landscape of cytotrophoblasts from normal and HDP placentas
Study
JGAS000667
-
ITER-FIISC Data Access Committee (Sepsis)
Dac
EGAC50000000641
-
INdiana GENomics: Implementing an Opportunity for the Under Served (INGENIOUS)
Study
phs001701
-
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients.
Study
JGAS000166
-
Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
-
Single-cell RNA-seq of human kidney tumors
Study
EGAS00001006534
-
Complex structural variation patterns in pediatric solid tumors
Study
EGAS00001007565
-
mRNA-seq data from ALL patients with NUP214::ABL1 disease
Dataset
EGAD50000001395
-
Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer
Study
EGAS50000000284
-
Comprehensive genetic analysis of pediatric germ cell tumors
Study
JGAS000204
-
Hyperfibrinolysis
Study
EGAS00001000104
-
Bleeding
Study
EGAS00001000106
-
Various_Platelet_Disorders
Study
EGAS00001000107
-
Evaluation of capture and amplicon-based targeted sequencing methods on formalin-fixed tumours
Study
EGAS00001004965
-
WGS data for MMML for Study EGAS00001002199
Dataset
EGAD00001003274