-
Genomic platform specific polygenic risk scores impact breast cancer risk stratification
Study
EGAS00001008439
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing
Study
EGAS00001004760
-
Sequencing data for oesophageal and related samples - ICGC DCC release 26 (WGS)
Dataset
EGAD00001003580
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
Anaplastic meingioma methylation
Dataset
EGAD00010001629
-
Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus
Study
phs001654
-
Expression data from the Neo-CheckRay trial
Dataset
EGAD50000002552
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
-
Evolution of Structural Rearrangements in Prostate Cancer Intracranial Metastases
Study
phs003357
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study
Study
phs001398
-
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Study
phs002033
-
RNAseq dataset
Dataset
EGAD50000001243
-
Pancreatic adenocarcinoma QCMG 20110901
Dataset
EGAD00001000049
-
Small‑scale mutations are infrequent as mechanisms of resistance in post‑PARP inhibitor tumour samples in high grade serous ovarian cancer
Study
EGAS50000000146
-
Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
Study
EGAS00001005071
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
H3Africa H3AChipDesign Phenotype
Dataset
EGAD00001005310
-
Heart and Vascular Health Study (HVH)
Study
phs001013
-
10x Genomics raw data of intestinal plasma cells
Dataset
EGAD50000000342
-
Prostate cancer datasets WES
Dataset
EGAD00001004467
-
A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data
Study
EGAS00001002428
-
Ischemic Stroke Genetics Study (ISGS)
Study
phs000102
-
BrainCloud: Data from human postmortem brain procurement for the neuropathology section
Study
phs000417
-
WGS data of patient derived organoids (PDO) generated from dMMR colorectal tumor subclones
Dataset
EGAD50000000427
-
Discovery and Characterization of Genetic Risk Loci in Sjogren's Syndrome
Study
phs002723
-
MicroRNAs, Hypertension and End Organ Damage in Humans
Study
phs002389
-
DNA Methylation in Prostate Tumor and Paired Benign Tissue for African and European Ancestry Men
Study
phs003516
-
Single cell RNA sequencing data of advanced melanoma patients treated with checkpoint inhibitor immunotherapy
Dataset
EGAD50000000493
-
Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Study
EGAS00001002390
-
Prostate cancer datasets WGS
Dataset
EGAD00001004466
-
Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis
Study
phs001743
-
Whole Exome Sequencing of Human Gastro-esophageal Cancer PDXs
Dataset
EGAD50000001407
-
Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn.
Study
EGAS00001002207
-
Prospective high-throughput genome profiling in advanced cancers:
Study
EGAS00001004554
-
A Retrospective and Cross-Sectional Analysis of Patients Treated for SCID Since January 1, 1968
Study
phs001326
-
WGS in insulinomas
Dataset
EGAD50000000464
-
Transcriptomic profiling of patient-derived xenografts and organoids in prostate cancer
Dataset
EGAD00001006404
-
National Cancer Institute (NCI) Early Onset Malignancies Initiative (EOMI): Molecular profiling of Breast, Colon, Kidney, Liver, Multiple Myeloma, and Prostate among Racially and Ethnically Diverse Populations
Study
phs001952
-
The Mutational Landscape of CTCL and Sezary Syndrome
Study
phs000994
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Dataset
EGAD00001009972
-
Heart Failure Network: Entresto(TM) in Advanced Heart Failure (HFN-LIFE-BioLINCC)
Study
phs004171
-
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Study
phs000433
-
National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci
Study
phs000168
-
Genes and Blood Clotting Study (GABC)
Study
phs000304
-
Mutation analysis of 17 genes in plasma DNA of CRC patients using the AVENIO ctDNA Targeted Kit
Dataset
EGAD00001006103
-
Neuroblastoma_MP-PCR_MultiplexPCR_TargetedSequencing_BAMs
Dataset
EGAD50000002260
-
ATACseq - Notch Signaling Maintains a Progenitor-Like Subclass of Hepatocellular Carcinoma
Study
EGAS50000000516
-
RNA sequencing from High-grade B-cell lymphoma, not otherwise specified: an LLMPP study
Dataset
EGAD50000001365
-
Sequencing data for oesophageal and related samples - OACs release 2 (RNA)
Dataset
EGAD00001003839