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Meningioma Exome
Dataset
EGAD00001000099
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Breast Cancer Exome Sequencing
Dataset
EGAD00001000110
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HER2 positive Breast Cancer
Dataset
EGAD00001000126
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DATA FILES FOR SJPHALL
Dataset
EGAD00001000163
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Tumor sample of a serious ovarian carcinoma
Dataset
EGAD00001000139
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Blood sample of serious ovarian carcinoma patient
Dataset
EGAD00001000140
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Xenograft Seqeuncing
Dataset
EGAD00001000143
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Deep sequencing of CTCs
Dataset
EGAD00001000220
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DNA sequencing of samples from normal tissue of colon biopsies
Dataset
EGAD00001000642
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DNA sequencing of samples from tumoural tissue of colon biopsies
Dataset
EGAD00001000643
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The FF bladder signature conservation set
Dataset
EGAD00001000833
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The paired FF/FFPE bladder set
Dataset
EGAD00001000832
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The paired FF/FFPE prostate set
Dataset
EGAD00001000830
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Strand-specific RNA Sequencing of paired initial and recurrent gliomas
Dataset
EGAD00001001613
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oceoadapto_seanomad
Dataset
EGAD00010001200
-
REL-2017-07-2016
Dataset
EGAD00010001366
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REL-2017-07-2007
Dataset
EGAD00010001348
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REL-2017-07-2008
Dataset
EGAD00010001350
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REL-2017-07-2009
Dataset
EGAD00010001352
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iOmics_genomic_data
Dataset
EGAD00010001309
-
REL-2017-07-2010
Dataset
EGAD00010001354
-
REL-2017-07-07
Dataset
EGAD00010001356
-
REL-2017-07-2014
Dataset
EGAD00010001362
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REL-2017-07-2015
Dataset
EGAD00010001364
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microRNA
Dataset
EGAD00010001406
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RHD_NC_HC24_Cases
Dataset
EGAD00010000957
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Southeast_Borneo_730K
Dataset
EGAD00010000944
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dataset1
Dataset
EGAD00010001012
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HMEC Non-label-retaining cells
Dataset
EGAD00010001966
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MCF10A 24h IL6 trans-signaling
Dataset
EGAD00010001969
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A3164_ClariomD
Dataset
EGAD00010001705
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native_american_pops_Axiom_Human_Origins
Dataset
EGAD00010001803
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tupiniquim_guarani_Axiom_InCor_BB
Dataset
EGAD00010001802
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MCF10A 12h IL6 trans-signaling
Dataset
EGAD00010001960
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Hydroxycarbamide effect on DNA methylation_CD34
Dataset
EGAD00010001941
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Finland-Immuno
Dataset
EGAD00010002048
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colon
Dataset
EGAD00010002200
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Genotype_controls
Dataset
EGAD00010002340
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PDAC-Microarray-Clariom-S-data
Dataset
EGAD00010002443
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FRONTIER DNA methylation
Dataset
EGAD00010002182
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Aboriginal Genetics and Health Studies based at the Telethon Kids Institute, Perth, Western Australia
Dac
EGAC00001000261
-
Methylation_WB_RA
Dataset
EGAD00010002610
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INCLIVA-CC-panel DAC
Dac
EGAC50000000061
-
Idiopathic Collapsing Glomerulopathy - Brazil
Dac
EGAC50000000012
-
This DAC takes care of requests for data for the Swiss epigenetic colorectal cancer cohort study, SWEPIC
Dac
EGAC00001003471
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Ultra-deep targeted sequencing for studying the accumulation of somatic mutations in cancer-free human skin
Study
EGAS00001004279
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A population specific reference genome defined from the analysis of 153 United Arab Emirates nationals.
Study
EGAS00001004537
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Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia
Study
EGAS00001003701
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Healthy_pleura
Dataset
EGAD00010002656
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Pleural_mesothelioma
Dataset
EGAD00010002657
-
Buccal sample methylation from breast cancer cases
Dataset
EGAD00010002635
-
Methylation_cfDNA_cancer
Dataset
EGAD00010002587
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Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia
Study
EGAS00001006878
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Illumina MethylationEPIC Repeatability dataset
Dataset
EGAD00010002501
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NanoString Panel Standard
Dataset
EGAD00010002431
-
NanoString Cancer
Dataset
EGAD00010002432
-
GWAS data of the AlpeDPD study
Dataset
EGAD00010002684
-
Dataset for the spanish node
Dataset
EGAD50000000884
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DAC Department of Neurology, TUM University Hospital, Technical University of Munich, School of Medicine and Health
Dac
EGAC00001003508
-
PBAT sequencing of cytotrophoblast and mural trophectoderm
Dac
EGAC50000000424
-
Preliminary Results from the Initiative for Molecular Profiling and Advanced Cancer Therapy 2 (IMPACT 2) Study
Study
EGAS00001004964
-
MutationalPatterns2: The one stop shop for the analysis of mutational processes: DNA repair deletions
Study
EGAS00001004789
-
Hepatocellular carcinoma xenografts established from needle biopsies preserve the characteristics of the originating tumors
Study
EGAS00001003396
-
Genomic insight into the origins and dispersal of the Brazilian Coastal Natives
Study
EGAS00001004036
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Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients
Study
EGAS00001004115
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High coverage sequencing of a single sample can account for the problem of intratumor heterogeneity
Study
EGAS00001004200
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: Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumours
Study
EGAS00001004239
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Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.
Study
EGAS00001004320
-
Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo
Study
EGAS00001004365
-
Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes
Study
EGAS00001004502
-
Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer
Study
EGAS00001005242
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Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Study
EGAS00001005401
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SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria
Study
EGAS00001005448
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IN UTERO ORIGIN OF MYELOFIBROSIS PRESENTING IN ADULT MONOZYGOTIC TWINS AFTER A PROLONGED DISEASE LATENCY
Study
EGAS00001005744
-
S3 Swedish schizophrenia case-control study
Study
EGAS00001006772
-
A capture-based next-generation sequencing panel for the molecular characterization of chronic lymphocytic leukemia
Study
EGAS00001006975
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Baseline RNAseq analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67
Study
EGAS00001007302
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The genomic echoes of the last Green Sahara on the Fulani and Sahelian people
Study
EGAS00001007499
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Neoantigen Peptides derived from V(D)J-recombined Immunoglobulins Drive Outgrowth of Cytolytic CD8+ T-cells
Study
EGAS00001008229
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Karolinska Institutet - Susanne Schlisio Lab
Dac
EGAC50000000603
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IRCC
Dac
EGAC50000000068
-
Institute of Pathology at the University Hospital of Lausanne CHUV
Dac
EGAC50000000314
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Transposable elements are co-opted as oncogenic regulatory elements by lineage-specific transcription factors in prostate cancer
Study
EGAS00001007188
-
Transcriptome analysis of leiomyosarcoma
Study
EGAS50000000594
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Transcriptomic profiling of prostate cancer metastasis xenograft models reveals conservation of bone microenvironment signatures
Study
EGAS00001004770
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BIOCLOCK Study Methylation Data
Dataset
EGAD00010002801
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SNParray_BadBRCA
Dataset
EGAD00010002734
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Epigenetic reprogramming shapes monocytes and heterologous T cell derived cytokine responses in BCG vaccination
Study
EGAS00001007498
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Homologous recombination DNA repair deficiency and activity of PARP inhibition in primary triple negative breast cancer
Study
EGAS00001004190
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Next Generation Sequencing Characterization of Hematopoietic Stem and Progenitors Cells in Human Systemic Lupus Eryhtematosus
Study
EGAS00001003679
-
Altered neutrophil and granulopoiesis biology underlie a poor outcome sepsis endotype
Study
EGAS00001006283
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Multi-modal analysis of pediatric pilocytic astrocytomas reveals tumor location-associated cellular and transcriptional heterogeneity
Study
EGAS00001008187
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Orolova hIPSC data access policy
Dac
EGAC50000000744
-
Oncolytic virotherapy mediated anti-tumor response in primary cutaneous B-cell lymphoma: a single-cell perspective
Study
EGAS00001004904
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Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells.
Study
EGAS00001006141
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IG-MYC rearrangement defines a high-risk subgroup of B-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001005111
-
Anaplastic_Meningioma_V3__cancer_gene_panel
Study
EGAS00001001155
-
PAGE2 Dataset Nov 2017 (Ref: PAGE2 GIM 2018)
Dataset
EGAD00001004842
-
RNA-seq PE
Study
EGAS00001006522
-
Bulk RNAseq of mCRC organoids
Study
EGAS00001006727