-
Mutational Study Committee of a Taiwanese Lung Cancer Cohort (MSCTLCC)
Dac
EGAC00001001614
-
A MITF germline mutation predisposes to melanoma and renal cell carcinoma
Study
EGAS00000000048
-
A body map of somatic mutagenesis in morphologically normal human tissues (WES)
Study
EGAS00001005459
-
Obesity and hyperinsulinemia drive adipocytes to activate a cell cycle program and senesce
Study
EGAS00001005770
-
Genomic Landscape of Follicular Lymphoma Across a Wide Spectrum of Clinical Behaviors
Study
EGAS00001007105
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001002303
-
DAC for Sarcopenia HNSCC
Dac
EGAC50000000420
-
Center for Technology Licensing at Cornell University for data associated with Nature Medicine 2024 paper
Dac
EGAC50000000207
-
Identification of biomarkers for prediction of efficacy of microtubule inhibitors and antifolates in non-small cell lung cancer
Study
JGAS000267
-
GoT2D WGS analysis files
Dataset
EGAD00010001185
-
Hi-C and promoter capture Hi-C data
Dataset
EGAD00001003257
-
DNAmet
Study
EGAS50000001051
-
miRNA seq
Study
EGAS50000001050
-
FASTQ files of the RNA-Seq data for the study "Genomic landscape of lung adenocarcinoma in East Asians"
Dataset
EGAD00001004421
-
FASTQ files of the Exome-Seq data for the study "Genomic landscape of lung adenocarcinoma in East Asians"
Dataset
EGAD00001004422
-
Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053
-
January 2016 update of RNA-Seq data 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
EGAD00001001885
-
ChIP-Seq (H3K4me3, H3K4me1, H3K9me3, H3K27ac, H3K27me3, H3K36me3, Input) data for HL60 cell line generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency.
Dataset
EGAD00001002238
-
Chromatin 3D interactions mediate genetic effects on gene expression (ChIP-seq)
Dataset
EGAD00001004871
-
Dataset for white blood cell and cell-free DNA analyses for detection of residual disease in gastric cancew
Dataset
EGAD00001005750
-
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
-
The dataset for Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Dataset
EGAD00001010891
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Phase 1/2 Study of the Indoleamine 2,3-Dioxygenase 1 Inhibitor Linrodostat Mesylate Combined With Nivolumab or Nivolumab and Ipilimumab in Advanced Solid Tumors or Hematologic Malignancies
Study
EGAS50000000710
-
DAC for study Screening for abnormal CGI methylation in primary colorectal tumours
Dac
EGAC00001000069
-
Data Access Committee for German Consortium for Translational Cancer Research (DKTK)
Dac
EGAC00001000217
-
Data Access Committee for COLO829 Somatic reference standard for cancer genome sequencing
Dac
EGAC00001000408
-
ATACseq
Study
EGAS00001007166
-
SNParray
Study
EGAS00001004979
-
WTCCC case-control study for Multiple Sclerosis
Study
EGAS00000000022
-
WTCCC case-control study for Breast cancer
Study
EGAS00000000024
-
WTCCC case-control study for Ankylosing Spondylitis
Study
EGAS00000000018
-
cfDNA dataset for cfDNA cohort
Dataset
EGAD50000000104
-
Targeted sequencing analysis for MDS with HSCT
Study
EGAS00001001949
-
A body map of somatic mutagenesis in morphologically normal human tissues (WGS)
Study
EGAS00001005458
-
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - WGS
Study
EGAS00001006843
-
EGAD00000000029
Dataset
EGAD00000000029
-
EGAD00000000028
Dataset
EGAD00000000028
-
Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation
Study
EGAS00001004934
-
20200819_EGA_Qld_Melanoma.radiomics
Dataset
EGAD00001006375
-
Chromosomal instability shapes the tumor microenvironment of oesophageal adenocarcinoma via a cGAS–chemokine–myeloid axis
Study
EGAS50000001561
-
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Study
EGAS50000000298
-
Transcriptome analysis of human iPSC-derived microglia in a novel human 3D cortical tissue model
Study
EGAS50000000469
-
RNAseq of 704 patients with soft tissue tumors
Dataset
EGAD50000002120
-
Chondrosarcoma Targeted Sequencing Study
Dataset
EGAD00001000265
-
Osteosarcoma Targeted Sequencing Study
Dataset
EGAD00001000266
-
Chordoma Targeted Sequencing Study
Dataset
EGAD00001000267
-
Meningioma Targeted Sequencing Study
Dataset
EGAD00001000273
-
Cholesterol homeostasis and lipid raft dynamics at the basis of tumor-induced immune dysfunction in chronic lymphocytic leukemia
Study
EGAS50000000933
-
DAC for access to anonymised study data for UK and Norwegian AAD families
Dac
EGAC00001000333
-
monozygotic twin discordant for schizophrenia
Dataset
EGAD00001000048
-
Dac for "Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)"
Dac
EGAC50000000072
-
WTCCC case-control study for Autoimmune Thyroid Disease
Study
EGAS00000000020
-
Genomic sequencing data for PNG15 and PNG16
Study
EGAS50000001105
-
WGS data for cfDNA cohort
Dataset
EGAD50000000102
-
WES dataset for cfDNA cohort
Dataset
EGAD50000000103
-
Validation for human early embryonic substitutions (2015_09_03)
Dataset
EGAD00001001600
-
Whole genome sequencing and transcriptome sequencing data for Burkitt lyphomas
Dataset
EGAD00001005781
-
Single-cell dissection of the immune response after a myocardial infarction
Study
EGAS00001007021
-
Biological and Therapeutic Implications of a Unique Subtype of NPM1 Mutated AML
Study
EGAS00001004872
-
CRISPR-based adenine editors correct nonsense mutations in a cystic fibrosis organoid biobank.
Study
EGAS00001003951
-
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS
Study
EGAS00001006800
-
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq
Study
EGAS00001006802
-
Study on longer adjuvant chemotherapy in Women with Early Breast Cancer
Study
phs000807
-
Genomic Analysis of Metastatic Brain Cancer
Study
phs002639
-
NHLBI TOPMed - NHGRI CCDG: Penn Medicine BioBank Early Onset Atrial Fibrillation Study
Study
phs001601
-
Elevated circulating tumor cells reflect high proliferation and genomic complexity in multiple myeloma - RNA validation cohort
Study
EGAS50000001212
-
Elevated circulating tumor cells reflect high proliferation and genomic complexity in multiple myeloma - WGS validation cohort
Study
EGAS50000001211
-
Extrachromosomal DNA-driven oncogene dosage heterogeneity determines therapy response in neuroblastoma
Study
EGAS50000001040
-
3D chromatin contacts of iPSC (controls) and mDAN (differentiated neurons) cells
Study
EGAS50000001578
-
single cell RNA-seq of small cell lung cancer tumors
Study
EGAS50000001400
-
Genomic profiling of Rare Tumors Release 2
Study
EGAS50000000615
-
PASCAL-MID Targeted amplicon sequencing of CD34+ HSPCs (CGD)
Dataset
EGAD50000001651
-
WES of Bipolar cases and controls performed at the Broad Inst on cohort from Cardiff, UK (Craddock)
Dataset
EGAD50000000547
-
A comprehensive DNA methylation landscape of human and mouse cell lines derived from hematological malignancies
Dataset
EGAD50000000888
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
Breast_cancer_sequential_sampling_study
Study
EGAS00001000300
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
Whole exome sequencing of trio with primary immunodeficiency (IL2RB)
Study
EGAS00001003599
-
HipSci_RNASEQ_Retinitis_Pigmentosa
Study
EGAS00001001996
-
Targeted_sequencing_of_cylindroma_patients
Study
EGAS00001002708
-
Tumor intrinsic and extrinsic mechanisms of response and resistance to blinatumomab in relapsed/refractory acute lymphoblastic leukemia
Study
EGAS00001004027
-
Whole-genome low pass sequencing of 3,514 Sardinian individuals
Study
EGAS00001002212
-
Melanoma C32 ENU Resistance to Single Agent Therapy
Dataset
EGAD00001003239
-
Hyperhaploid multiple myeloma
Dataset
EGAD00001004328
-
Genomic profiling of Rare Tumors
Study
EGAS00001007103
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
cfDNA
Dataset
EGAD00001006566
-
Genome and transcriptome sequence data from a peritoneal mesothelioma patient
Dataset
EGAD00001001310
-
Genome and transcriptome sequence data from a peritoneal mesothelioma patient
Dataset
EGAD00001001311
-
Genome and transcriptome sequence data from a parotid gland cancer patient
Dataset
EGAD00001001657
-
Trimmed bam-files from whole genome sequencing data from plasma DNA
Dataset
EGAD00001002254
-
Genome and transcriptome sequence data from a locally advanced breast cancer patient
Dataset
EGAD00001004897