-
Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ)
Study
phs000718
-
NIDDK IBD Genetics Consortium Repository Immunochip
Study
phs001721
-
Tandem DNA Repeats Activate hTERT Gene Transcription
Study
phs002428
-
PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Study
phs003475
-
DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia
Study
phs001963
-
Joint-Specific TF Regulation in RA
Study
phs003633
-
Pre-Existing Skin-Resident CD8 and γδ T Cell Circuits Mediate Immune Response in Merkel Cell Carcinoma and Predict Immunotherapy Efficacy
Study
phs003629
-
Chronic Renal Insufficiency Cohort (CRIC) - GWAS
Study
phs000524
-
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Study
JGAS000002
-
Genomic and Genetic Analysis of Brain Tumors and Analysis of Their Clinicopathological Significance
Study
JGAS000004
-
Emergence of oncofetal plasticity is ubiquitous in early colorectal cancers
Study
EGAS50000001532
-
Hematopoietic Tet2 inactivation enhances the response to checkpoint blockade immunotherapy
Study
EGAS50000001191
-
Patient-derived pediatric brain tumor organoids faithfully recapitulate primary tumors
Study
EGAS00001008305
-
Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Study
EGAS00001005268
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Myeloid cell networks govern re-establishment of original immune landscapes in recurrent ovarian cancer
Study
EGAS50000001069
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
-
Pooled scRNA-seq of iPSC-derived neural stem cells from ADHD and control individuals
Study
EGAS00001008169
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3
Study
EGAS00001004798
-
Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection
Study
EGAS00001006909
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
-
Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes
Dataset
EGAD00001006231
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
Genetic drivers of epigenetic and transcriptional variation of human immune responses to infection (RNA-seq, ATAC-seq and ChIPmentation)
Dataset
EGAD00001008422
-
A Tumour Organoid Biobank for Mapping Cancer Cell Vulnerabilities - WGS
Dataset
EGAD00001015469
-
Caregiving as a Natural Stressor in Studies of the Role of Genes That Affect Serotonin Function in Regulating Risk Factors for Coronary Heart Disease (CAREGIVER)
Study
phs001747
-
Characterization of a New Case of XMLV (Bxv1) Contamination in the Human Cell Line Hep2 (Clone 2B) Using High-Throughput DNA- and RNA-Seq
Study
phs001944
-
Impact of Mutated CTCF DNA binding sites of Topologically associating domains on nearby Cancer Gene Regulation: A Multi-Omics Analysis
Study
EGAS50000001686
-
Identification of fusion transcripts by RNA-sequencing and Whole genome sequencing of a METABRIC patient sample
Study
EGAS00001002475
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
16S rRNA gene V4 region sequencing data, ASV profiles, and sample metadata of human faecal samples predominantly from the Estonian population
Dataset
EGAD50000002306
-
SUM-seq data for spontaneously differentiated iPSCs to EBs
Dataset
EGAD50000001589
-
Single-Cell and Bulk RNA Sequencing of Oncolytic Measles Virus Treatment in Pediatric Medulloblastoma and ATRT
Dataset
EGAD50000001197
-
Long-read whole genome sequencing as a tool for variant detection in inherited retinal dystrophies
Dataset
EGAD50000001238
-
scRNA-seq of human follicular lymphoma and lymph node
Dataset
EGAD50000001143
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Dataset
EGAD50000000679
-
EGAD00010000766
Dataset
EGAD00010000766
-
Frequent mutation of the major cartilage collagen gene, COL2A1, in chondrosarcoma
Dataset
EGAD00001000358
-
Myelodysplastic Syndrome Follow Up Series
Dataset
EGAD00001000283
-
Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics
Dataset
EGAD00001003705
-
10x dataset of an obese human subject
Dataset
EGAD00001005101