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Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176
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Clonal origin of lineage switch leukemia following CAR-T cell and blinatumomab therapy
Dataset
EGAD00001009161
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DERMATLAS: Hidradenoma papilliferum_RNAseq
Dataset
EGAD00001015480
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Epigentic sequence data of monocytes and macrophages
Dataset
EGAD00001002201
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Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Dataset
EGAD00001009647
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The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments. (2019-06-10)
Dataset
EGAD00001005082
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PacBio Rare Disease Study
Dataset
EGAD00001015611
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DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Dataset
EGAD00001009668
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Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
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ESGI-Exome sequencing in Circulating Tumor Cells to determine therapy related markers
Dataset
EGAD00001001425
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RNAseq Atlas in HCC tumors
Dataset
EGAD00001015341
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Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - WGS
Dataset
EGAD00001009793
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Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - RNA-Seq
Dataset
EGAD00001009794
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Triple Negative Breast Cancer RNA Sequencing
Dataset
EGAD00001000390
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Chromatin 3D interactions mediate genetic effects on gene expression (ChIP-seq)
Dataset
EGAD00001004871
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Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Dataset
EGAD00001009847
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NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
FinHer Breast Cancer Study
Dataset
EGAD00001000871
-
Genomic Advances in Sepsis (GAinS) genotyping
Dataset
EGAD00001015369
-
Human Origins array data for 1510 individuals
Dataset
EGAD00001010015
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS)
Dataset
EGAD00001003130
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Dataset
EGAD00001003246
-
The molecular landscape of colorectal cancer reveals genetic mutations(17 cases)
Dataset
EGAD00001003224
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Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Dataset
EGAD00001003315
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Dataset of whole genome bisulfite data of 4 different monocyte samples
Dataset
EGAD00001003259
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Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
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Genetic factors underlying premature MI in Greek families without vessel disease
Dataset
EGAD00001002178
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (RNA-Seq for CD4-positive, alpha-beta T cell, on genome GRCh37)
Dataset
EGAD00001002671
-
Genetic profiling of mucosal melanoma
Dataset
EGAD00001003237
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)
Dataset
EGAD00001005017
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
GNAI1 CGH Array
Dataset
EGAD00001007742
-
Xenograft BC WGS Dataset
Dataset
EGAD00001001336
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Next gen seq of eye cancers (2019-08-14)
Dataset
EGAD00001005251
-
Congenital mesoblastic nephroma and infantile fibrosarcoma
Dataset
EGAD00001003885
-
Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884
-
February 2021 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001007919
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cells, (ChIP-Seq_H3K4me3 for mature neutrophil, on genome GRCh37)
Dataset
EGAD00001002711
-
Somatic mutations of 256 whole-genome sequenced colorectal cancer tumors.
Dataset
EGAD00001004329
-
September 2016 data update (bam/fastq/vcf) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001002724
-
BASIS RNAseq
Dataset
EGAD00001001264
-
Low coverage whole-genome sequencing of samples from the Cretan Greek isolate collection HELIC-MANOLIS
Dataset
EGAD00001001637
-
DNMT3A-R882 mutations intrinsically drive dysfunctional neutropoiesis from human haematopoietic stem cells
Dataset
EGAD00001015750
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
HSP90 inhibitor resistant K562 cells
Dataset
EGAD00001009051
-
Understanding the development of resident memory T cells (Trm) in the human small intestine using integrative multiomic approaches: Adult RNA (2025-10-14)
Dataset
EGAD00001015739
-
Balanced Ependymoma
Dataset
EGAD00001000350