-
Memorial Sloan Kettering (MSKCC) Single Cell Mutational Profiling in Myeloid Malignancies
Study
phs002049
-
Osteosarcoma Genomics
Study
phs000699
-
Genomics of Hepatocellular Carcinoma
Study
phs001106
-
Transformation of Dysplasia in Barrett's Esophagus
Study
phs002706
-
Heterogeneity in Lysosomal Storage Disorders
Study
phs003459
-
Re-Evaluation of Systemic Early Neuromuscular Blockade
Study
phs003929
-
Chromatin remodeling enhances MAP3K8 expression in HAM: a key pathogenesis for therapeutic intervention
Study
JGAS000835
-
Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Study
EGAS00001002743
-
Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment
Study
EGAS00001002485
-
Novel CNV contribution to schizophrenia from a genome wide study of 41,321 subjects
Study
EGAS00001001960
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002643
-
Cerebral organoid model reveals excessive proliferation of human caudal late interneuron progenitors in Tuberous Sclerosis Complex
Study
EGAS00001004586
-
Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002642
-
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Study
EGAS00001003870
-
5- FU treated organoids
Study
EGAS00001003592
-
MutWP1__CRUK_Grand_Challenge__matched_blood_Nanoseq
Study
EGAS00001006774
-
MutWP1__CRUK_Grand_Challenge__normal_kidney_Nanoseq
Study
EGAS00001005451
-
Machine Learning Signal Enrichment for Ultrasensitive Plasma Tumor Burden Monitoring
Study
EGAS00001007451
-
PD-L1 blockade immunotherapy rewires cancer-induced emergency myelopoiesis
Study
EGAS00001007873
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450
-
CYP2C19 long-read sequencing
Study
EGAS00001006929
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring
Study
EGAS00001007545
-
RRBS data (cfSort study) from noncancer tissue DNA
Dataset
EGAD00001010880
-
Somatic Mutations in Variant and IGHV4-34 Expressing Hairy Cell Leukemia
Study
phs000671
-
Tumor heterogeneity and acquired drug resistance in FGFR2 fusion-positive cholangiocarcinoma through rapid research autopsy
Study
phs001830
-
Single-cell genotype-to-phenotype mapping via co-capture of DNA mutations and mRNA transcripts
Dac
EGAC50000000833
-
RGB TGCT Data Access Committee
Dac
EGAC50000000959
-
Autosomal dominant macular dystrophy associated with THRB: identification of new families and variants 
Study
EGAS50000000861
-
Clinical and molecular features of early onset pancreatic cancer
Study
EGAS50000000362
-
Long-read Nanopore and Ion Torrent sequencing data for BRCA1/2 variant detection
Dac
EGAC50000000946
-
PDAC clinical phenotype data with CA19-9 and Lewis antigen status
Dataset
EGAD50000002254
-
Raw scTCR-seq data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Dataset
EGAD50000002191
-
Raw scRNA-seq data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Dataset
EGAD50000002190
-
scRNAseq dataset of circulating T cells in FL patient before and after Lenalidomide treatment
Dataset
EGAD50000001529
-
RNA-sequencing of PBMCs from COVID-19 patients experiencing different degrees of the disease (mild and critical), and control patients
Dataset
EGAD50000001405
-
NICOLA QUB Genetic
Dataset
EGAD00010002762
-
ETMR_Meth
Dataset
EGAD00010001669
-
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
-
Transcriptome (RNA-seq) data for the validation of the glioblastoma progression study (GBMatch).
Dataset
EGAD00001004076
-
Genomic (WGS) data for the validation of the glioblastoma progression study (GBMatch).
Dataset
EGAD00001004077
-
Delineate genomic and epigenomic changes in esophageal squamous cell carcinoma following radiotherapy
Dataset
EGAD00001003799
-
Whole genome sequencing data from whole genome amplified single cells and unamplified bulk samples
Dataset
EGAD00001004195
-
Whole genome sequencing of paired samples from primary and relapsed IDH-wt glioblastomas with matched blood controls
Dataset
EGAD00001004563
-
Exome data: Histone mutations in human Pre-Leukemic HSC and AML
Dataset
EGAD00001004436
-
Edinburgh Naevi Cohort (2018-08-03)
Dataset
EGAD00001004273
-
Whole genome sequencing of 40 gastric cancer tumours and matched normal samples from Singapore.
Dataset
EGAD00001004279
-
Whole Exome (WE) sequencing data files for H_NO-JB001
Dataset
EGAD00001001252