-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
Assessment of de novo copy number variations in Italian patients with schizophrenia.
Study
EGAS00001002159
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Study
EGAS00001004064
-
nanostring_gene_expression
Dataset
EGAD00010002654
-
Whole exome sequencing variant data for Mendelian disorders cohort
Dataset
EGAD50000002453
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Dataset
EGAD00001006291
-
Whole-exome sequences of ovarian clear cell carcinomas and paired normal DNA
Dataset
EGAD00001006004
-
Single-cell atlas of the human healthy airways
Dataset
EGAD00001005714
-
PacBio Rare Disease Study
Dataset
EGAD00001015611
-
Thirty cutaneous SCC WES tumour samples with matched normal
Dataset
EGAD00001002253
-
Glioblastoma CRISPR Screen (2017-04-27)
Dataset
EGAD00001003308
-
Sequencing data for ICGC Oesophageal Adenocarcinoma tissue samples - 100
Dataset
EGAD00001001071
-
Whole-exome sequencing of liver cancer organoids
Dataset
EGAD00001004205
-
Myeloid gene panel or whole exome sequencing data on blood and bone marrow of 15 individuals with germline RUNX1 mutations to characterize additional somatic mutations.
Dataset
EGAD00001006010
-
A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
Dataset
EGAD00001006190
-
National Cancer Institute (NCI) Prostate Cancer Genome-Wide Association Study for Uncommon Susceptibility Loci (PEGASUS)
Study
phs000882
-
eIMPACT Trial: Modernized Collaborative Care to Reduce the Excess CVD Risk of Older Depressed Patients
Study
phs003283
-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
LCLF1.0 Data
Study
phs003187
-
RB1 Gene Inactivation by Chromothripsis in Human Retinoblastoma
Study
EGAS00001000598
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - TGS
Dataset
EGAD00001010874
-
Whole Genome Sequencing of HCC
Dataset
EGAD00001003994
-
(RNA-seq) Shifted assembly and function of mSWI/SNF family subcomplexes underlie targetable dependencies in endometriod carcinomas
Dataset
EGAD50000001471
-
All counts
Dataset
EGAD50000001715
-
Long-read single-cell RNA-seq in COVID-19
Dataset
EGAD50000001836
-
Human lung cell atlas 10x and SS2 sequencing data (3 of 3)
Dataset
EGAD00001006128
-
Genomic and Transcriptomic Profile of Paired Primary-Metastasis Colorectal Tumors
Dataset
EGAD00001007686
-
Single nucleus RNA Seq of LUAD patient derived lung samples
Dataset
EGAD00001008955
-
Human lung cell atlas 10x and SS2 sequencing data (1 of 3)
Dataset
EGAD00001006126
-
MASQ targeted amplicon sequencing data of AML samples at presentation, remission, and relapse, and MASQ data demonstrating performance ranges of the method.
Dataset
EGAD00001005121
-
scRNAseq and scATACseq of MMR vaccinattion
Dataset
EGAD00001010012
-
Human lung cell atlas 10x and SS2 sequencing data (2 of 3)
Dataset
EGAD00001006127
-
pan-cancer plasma cfRNA
Dataset
EGAD00001009713
-
WES of breast and larynx cancer cases
Dataset
EGAD00001009081
-
Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy
Dataset
EGAD00001007787
-
CPC-GENE primary prostate benign and tumour tissue Hi-C sequencing reads
Dataset
EGAD00001008024
-
RNAseq of human fetal pancreas development
Dataset
EGAD00001004210
-
BLUEPRINT release August 2015, ChIP-Seq for germinal center B cell, on genome GRCh38
Dataset
EGAD00001001502
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000850
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000794
-
Effects of tobacco smoking on the tumor immune microenvironment in head and neck squamous cell carcinoma
Study
phs001994
-
Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation
Study
phs002143
-
Sensitive urothelial cancer detection via high volume urine DNA analysis
Study
EGAS50000000630
-
COVID-19-Induced Immune Alterations in Infants
Study
phs002655
-
Evolution of Structural Rearrangements in Prostate Cancer Intracranial Metastases
Study
phs003357
-
Whole genome sequencing data of paediatric T cell acute lymphoblastic leukemia (T-ALL)
Study
EGAS50000001387
-
Cardiogenics_re_sequencing
Study
EGAS00001000079
-
Chordoma_Sequencing_Project_RNAseq
Study
EGAS00001000410
-
Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns
Study
EGAS00001000043
-
Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns
Study
EGAS00001000050
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
Whole-genome cfDNA TAPS sequencing data from 91 people with various types of cancer and from non-cancer controls
Dataset
EGAD50000000996
-
WGS data of paediatric B-other B cell acute lymphoblastic leukemia (set1)
Dataset
EGAD50000002157
-
BLUEPRINT release August 2016, Bisulfite-Seq for Mantle Cell Lymphoma, on genome GRCh38
Dataset
EGAD00001002505
-
Whole genome sequencing of HSPCs and pAML
Dataset
EGAD00001006338
-
Hi-C in endometrial healthy and tumor tissues
Dataset
EGAD00001010898
-
ChIP sequencing data to study therapeutic targeting of ependymoma
Dataset
EGAD00001003979
-
BLUEPRINT release August 2014, Bisulfite-Seq for alternatively activated macrophage
Dataset
EGAD00001000920
-
BLUEPRINT release August 2016, Bisulfite-Seq for Multiple Myeloma, on genome GRCh38
Dataset
EGAD00001002521
-
A Phase I Study of the Treatment of Recurrent Malignant Glioma with CAN-3110 (AKA rQNestin34.5v.2), a Genetically Engineered HSV-1 Virus
Study
phs003378
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Study
EGAS50000001327
-
A single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas
Study
EGAS50000000342
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Study
EGAS00001001234
-
Sequencing of Infant high grade gliomas
Study
EGAS00001003532
-
Correction of a Factor VIII genomic inversion with designer recombinases
Study
EGAS00001005496
-
RP-1843 Arcagen - Gastrointestinal rare cancers (GI)
Study
EGAS00001006299
-
RNA-Seq in Patients with Primordial Dwarfism
Dataset
EGAD00001000640
-
SNP array
Dataset
EGAD00010002597
-
scRNAseq and scTCRseq of three tumor lesions derived from one patient receiving adoptive TIL therapy
Dataset
EGAD50000000406
-
miRNAseq of paired FL and tFL samples
Dataset
EGAD50000001385
-
colorectal_epigenome
Dataset
EGAD00010002726
-
STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
Dataset
EGAD50000002172
-
Transcriptome analysis of human muscle/myofibers carrying the human nemaline myopathy type 6-associated KBTBD13-R408C variant.
Dataset
EGAD50000002408
-
Omics data of advanced bladder cancer
Dataset
EGAD00001005978
-
WGS and RNA-Seq data of 2 additional patients of newly diagnosed multiple myeloma (NDMM)
Dataset
EGAD00001009627
-
Neuroblastoma WGS samples used for detection of seismic amplification
Dataset
EGAD00001007807
-
Exome reads
Dataset
EGAD00001003797
-
BLUEPRINT release August 2016, Bisulfite-Seq for plasma cell, on genome GRCh38
Dataset
EGAD00001002322
-
Resolving the Full Spectrum of Human Genome Variation using Linked-Reads
Dataset
EGAD00001004319
-
Longitudinal sequencing of a recurrent paediatric high grade neuroepithelial tumour
Dataset
EGAD00001004118
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Dataset
EGAD00001004157
-
Congenital Heart Disease in UK Families
Dataset
EGAD00001000343
-
Leiden_melanomafamilies
Dataset
EGAD00001002186
-
BLUEPRINT September 2016, ChIPmentation Burkitt Lymphoma from lymph node, on Genome GRCh38
Dataset
EGAD00001002939
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Dataset
EGAD00001003417
-
Data for Paper: Combining transcription factor binding affinities with open chromatin data for accurate gene expression prediction
Dataset
EGAD00001002735
-
Single cell RNA sequencing of colorectal cancer
Dataset
EGAD00001005198
-
RNA sequencing of cytokine-induced T cell responses
Dataset
EGAD00001005291
-
scRNAseq of patients with chronic graft-versus-host-disease
Dataset
EGAD00001012121
-
Innate Immune Anti-Viral Deaminase Deregulation Fuels Pre-Leukemia Stem Cell Evolution
Study
phs002228
-
Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
Study
JGAS000231
-
Characterization of a human iPSC-derived islet differentiation model
Study
EGAS00001002721
-
Pharmacological improvement of CFTR function rescues airway epithelial homeostasis and host defense in children with cystic fibrosis
Dataset
EGAD50000000173
-
Single cell chromatin accessibility profiles from myelofibrosis patients
Dataset
EGAD50000000234
-
Arcagen - NET / NEC G3
Dataset
EGAD50000000913
-
Human CMV-specific CD8+ T cells
Dataset
EGAD50000000894
-
EM-seq datatset of primary human thymocyte subsets
Dataset
EGAD50000001600
-
WGS data of conditional knockout mouse model mammary tumours
Dataset
EGAD50000002036