-
Benchmarking CRISPR Whole-genome Drop-out Screen - B&S (2019-08-07)
Dataset
EGAD00001005233
-
Regulatory Genomics of Human Embryonic Development
Study
phs001226
-
Searching for variants associated with endometriosis
Study
EGAS00001001741
-
CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia
Study
EGAS00001004808
-
Single nuclei RNAseq data from HGSOC primary tumour samples
Study
EGAS50000000249
-
Transcriptome of CD4+ T cells and CD8+ T cells in glioblastoma multiforme
Dataset
EGAD50000000226
-
POT1_splice_site_mutant_analysis
Study
EGAS00001000571
-
Enrichment Data
Dac
EGAC50000000346
-
Somatic pseudogenes acquired during cancer development – RNAseq
Dataset
EGAD00001000639
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing
Study
EGAS00001004832
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing
Study
EGAS00001004833
-
Mosaic structural variation sample
Study
EGAS50000000460
-
Copy Number Abnormalities of Chr1 in Multiple Myeloma at the Single Cell Level
Study
phs004109
-
The DIRECT study: A roadmap for ctDNA-based risk prediction, molecular profiling and MRD detection in Diffuse Large B Cell Lymphoma
Study
EGAS50000000968
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
Human Brain Small Extracellular Vesicles Contain Selectively-Packaged, Full-Length mRNA
Dataset
EGAD50000000042
-
WES+WGS OSCCs Boot et al. 2018
Study
EGAS00001003131
-
Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor
Study
phs001507
-
NIH RECOVER: A Multi-Site Pathology Study of Post-Acute Sequelae of SARS-CoV-2 Infection
Study
phs003768
-
Tracking early lung cancer metastatic dissemination in TRACERx using ctDNA
Study
EGAS00001006923
-
Long-read-transcriptome-sequencing of CLL and MDS patients uncovers common molecular effects of SF3B1 mutations
Study
EGAS50000000053
-
Spatial heterogeneity of follicular lymphoma
Dataset
EGAD00001003553
-
Women's Environmental Cancer and Radiation Epidemiology (WECARE) Study
Study
phs003945
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
WXS files for paper titled 'Genomic Landscape of Pediatric Myelodysplastic Syndromes'
Dataset
EGAD00001003781
-
Somatic pseudogenes acquired during cancer development – Whole Genome sequencing
Dataset
EGAD00001000638
-
Somatic pseudogenes acquired during cancer development – Whole Exome sequencing
Dataset
EGAD00001000637
-
Andersen-Tawil Syndrome: Genotype-phenotype correlation and longitudinal study
Study
phs001289
-
HGG panel sequencing
Study
EGAS50000000221
-
Understanding Determinants of Racial Disparities in Lung Cancer Incidence
Study
phs003789
-
RNAseq of 76 samples from Uveal Melanoma tumors
Study
EGAS00001002932
-
ICGC Prostate Cancer Whole Genome Sequencing
Dataset
EGAD00001000891
-
Woodcock et al TenMenDeep Study EGA Dataset B
Dataset
EGAD00001005382
-
Woodcock et al TenMenDeep Study EGA Dataset A
Dataset
EGAD00001005381
-
AfricanNeo WGS aDNA Dataset
Dataset
EGAD00001011320
-
Molecular Features of Hepatocellular Carcinoma Associated with 18F-Fluorocholine PET/CT Imaging Phenotype
Study
phs001784
-
Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer
Study
EGAS50000000793
-
A non-canonical lymphoblast in refractory childhood T-cell leukaemia
Study
EGAS50000000767
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
-
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
-
National Institute of Neurological Disorders and Stroke (NINDS), Family Study of Essential Tremor (FASET), Identification of Susceptibility Genes for Essential Tremor
Study
phs000966
-
GWAS results from Danjou et al, Nature Genetics 2015
Dataset
EGAD00010001722
-
International Parkinson's Disease Genomics Consortium (IPDGC), NeuroX Dataset
Study
phs000918
-
HTAN Pilot Project: Single-Cell Transcriptomics Toolbox for Fresh and Frozen Human Tumors (Lung, Breast, Ovarian, Melanoma, Neuroblastoma, Sarcoma, Glioblastoma, Glioma, and Leukemia)
Study
phs001983
-
Somatic Mutations in Individual Skin Cells
Study
phs003683
-
Whole exome sequencing of SU- DIPG-XIII from different sites
Dataset
EGAD00001003563
-
Veilleux et al. Human Subsistance - chemosensory genes
Dataset
EGAD00001010918
-
SCLC study Peifer et al. - WES dataset
Dataset
EGAD00001000703
-
He et al. WGS data
Dataset
EGAD00001007133