-
Follicular lymphoma shallow whole genome sequencing and targeted sequencing of lymphoma panel
Dataset
EGAD00001008385
-
NLG-LBC-05 ctDNA project sequencing data
Dataset
EGAD00001009337
-
sWGS of OV04 patient samples for ACN rascal study
Dataset
EGAD00001008121
-
Dataset for hematopoietic_malignancy-RNA
Dataset
EGAD00001008860
-
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Dataset
EGAD00001007997
-
Variation and transmission of the human gut microbiota across generations - shotgun data
Dataset
EGAD00001008207
-
Targeted Validation Samples
Dataset
EGAD00001010934
-
RNA sequencing in primary inflammatory (TPP) macrophages treated with a MEK1/2 inhibitor
Dataset
EGAD00001011337
-
Sequence data from stage I of the CCTG BR.36 ctDNA-directed, multi-center phase II study of molecular response adaptive immunotherapy in non-small cell lung cancer
Dataset
EGAD00001011359
-
Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Dataset
EGAD00001011360
-
RCC genomic data
Dataset
EGAD00001009866
-
WGS short read and 10X linked read sequencing of HR Deficient breast cancers
Dataset
EGAD00001010326
-
Machine Learning Guided Signal Enrichment for Plasma Tumor-burden Monitoring Dataset
Dataset
EGAD00001011352
-
Identifying autosomal recessive mutations causing neurological disorders
Dataset
EGAD00001000340
-
Identification of rare variants associated with cardiovascular traits in Cilento isolates
Dataset
EGAD00001002195
-
WTS data of patients diagnosed with NKTL
Dataset
EGAD00001005230
-
VariantMedium: Sensitive and generalizable somatic point mutation calling with 3D DenseNets trained and evaluated on experimental confirmation data
Study
EGAS50000001661
-
Effects of Metformin on Transcriptomic and Metabolomic Profiles in Breast Cancer Survivors Enrolled in the Randomized Placebo-Controlled MetBreCS Trial
Study
EGAS50000000874
-
How to use the EGA search box
Documentation
discovery/metadata/search-box
-
How upcycled prostate cancer sequences enabled key findings on telomeres length
Blog
prostate-cancer-sequences-enabled-key-findings-on-telomeres-length
-
Advancing fast in the analysis of circulating tumour DNA
Blog
advancing-fast-in-the-analysis-of-circulating-tumour-dna
-
Reading about genomic analysis of pan-neuroblastoma
Blog
genomic-analysis-of-pan-neuroblastoma
-
Youth-GEMs, the project using data to define the mental health trajectories of young people
Blog
youth-gems-mental-health
-
Breast Cancer Follow Up Series
Study
EGAS00001000002
-
Illumina Human Exome (ExomeChip) genotype data from the Pomak villages in Greece (HELIC Pomak Isolate). 1040 samples all >=16 years old.
Study
EGAS00001000658
-
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Study
EGAS00000000129
-
DO NOT USE - Whole genome sequencing of SI-NETs from five patients
Study
EGAS00001004435
-
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Study
EGAS00000000097
-
Department of Human Genetics, Radboud University Nijmegen Medical Centre, Data Access Committee
Dac
EGAC00001000076
-
Frequent mutation of the major cartilage collagen gene, COL2A1, in chondrosarcoma
Dataset
EGAD00001000358
-
13K T2D-GENES analysis files
Dataset
EGAD00010001188
-
Counts: Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Dataset
EGAD00010001457
-
UK_RCC_GWAS
Dataset
EGAD00010002310
-
GSA QCed data
Dataset
EGAD00010002568