-
Extreme intratumor heterogeneity and driver evolution in mismatch repair deficient gastro-esophageal cancer
Study
EGAS00001003434
-
PBMC gene expression profiles in diet treated celiac disease upon oral gluten challenge
Study
EGAS00001004860
-
Biological and Therapeutic Implications of a Unique Subtype of NPM1 Mutated AML
Study
EGAS00001004872
-
Inherited CD28 deficiency in otherwise healthy patients with disseminated warts and giant horns
Study
EGAS00001004837
-
Single cell RNA sequencing of 33 primary colorectal cancer
Study
EGAS00001003779
-
CRISPR-based adenine editors correct nonsense mutations in a cystic fibrosis organoid biobank.
Study
EGAS00001003951
-
The whole genome landscape of Burkitt lymphoma subtypes
Study
EGAS00001003778
-
Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia'
Study
EGAS00001005171
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma
Study
EGAS00001004288
-
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia
Study
EGAS00001005820
-
Longitudinal Single Cell Atlas of COVID-19 Identifies an Early, Transient Prognostic Signature
Study
EGAS00001005545
-
Minor intron splicing efficiency increases with the development of lethal prostate cancer
Study
EGAS00001005546
-
Absolute copy number fitting from shallow whole genome sequencing data
Study
EGAS00001005601
-
WGS of iPSC from TOF patients with/without DG and healthy control
Study
EGAS00001006035
-
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Study
EGAS00001006280
-
CDK4 phosphorylation predicts high sensitivity of malignant pleural mesotheliomas to CDK4/6 inhibition
Study
EGAS00001006117
-
miRNA regulation of monocyte expressed inflammatory genes in patients with inflammatory bowel disease
Study
EGAS00001006157
-
Serum Proteome Profiling Identifies Early Markers of Therapeutic Response to Neoadjuvant Chemotherapy of Breast Cancer
Study
EGAS00001006228
-
Genomics characterization of BRAF-V600E colorectal cancer patients treated with anti-BRAF/EGFR
Study
EGAS00001006247
-
Genetic Determinants of Mannose-binding Lectin Activity Predispose to Thromboembolic Complications in Critical COVID-19
Study
EGAS00001006266
-
Comprehensive Whole-Genome Sequence Annotation to Resolve the Genetic Architecture of Cerebral Palsy
Study
EGAS00001006724
-
Whole genome sequencing dataset of 200 trio families from the CHILD cohort study.
Study
EGAS00001006725
-
Tertiary lymphoid structure signatures are associated with immune checkpoint inhibitor related acute interstitial nephritis
Study
EGAS00001006781
-
The genome-wide mutational consequences of DNA hypomethylation
Study
EGAS00001006845
-
Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells
Study
EGAS00001007026
-
Gene expression of neutrophils in response to Mtb infection in persons living with HIV
Study
EGAS00001007262
-
Healthy human B-lymphopoiesis RNA-Seq reference using FACS sorted bone marrow aspirates
Study
EGAS00001007305
-
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans
Study
EGAS00001007423
-
DAC - A standardised framework for robust fragmentomic feature extraction from cell-free DNA sequencing data
Dac
EGAC00001003530
-
CReATe Fertility Centre DAC
Dac
EGAC50000000646
-
Single-cell dissection of the immune response after a myocardial infarction
Study
EGAS00001007021
-
PCF SELECT data on liquid biopsy samples from 3 clinical studies on prostate cancer patients
Dac
EGAC50000000758
-
Human glioblastoma single cell DAC (Linnarsson)
Dac
EGAC50000000575
-
Human developing meninges single cell DAC (Linnarsson)
Dac
EGAC50000000576
-
Asan Medical Center Data Access Committee
Dac
EGAC50000000733
-
Induction Failure in Childhood and Young Adult T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001006411
-
Accessibility Over Transposable Elements Reveals Genetic Determinants of Stemness Properties in Normal and Leukemic Hematopoiesis
Study
EGAS00001007191
-
KOLF2.1J human induced pluripotent stem cells-derived differentiated dopaminergic neurons (iPSC) Garcia-Swinburn et al.
Dac
EGAC50000000805
-
Hepatocellular Carcinoma Spatial transcriptomics Data Access Committee
Dac
EGAC50000000635
-
Pan Prostate Cancer Group Data Access Control Committee
Dac
EGAC50000000602
-
GenomeWideData_for_Present_Day_Peruvian_individuals_living_in_urban_areas
Dataset
EGAD00010002795
-
DAC SysMed
Dac
EGAC50000000089
-
Disturbed trophoblast transition links early fetal to maternal syndrome progression in pre-eclampsia
Study
EGAS00001005681
-
Genetic landscape of pediatric Retinoblastoma
Study
EGAS00001000346
-
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia
Study
EGAS00001005818
-
MOSAIC Window DAC
Dac
EGAC50000000398
-
X chromosome dosage and the impact on the methylation pattern across human tissues
Study
EGAS00001007020
-
Hypothesis Testing for Predictive Variables
Study
EGAS00001007763
-
DAC for Genetic and Microenvironmental Analysis of PTCL at Department of Hematology, University of Tsukuba
Dac
EGAC50000000600
-
Exome data for PDXs
Dataset
EGAD00001001863
-
dataset_CML_chipseq_pairend_bam
Dataset
EGAD00001002062
-
Exome reads
Dataset
EGAD00001003193
-
PPCG UK BAMs
Dataset
EGAD00001006742
-
dataset_CML_WGS_pairend_fastq
Dataset
EGAD00001002057
-
dataset_CML_chipseq_pairend_fastq
Dataset
EGAD00001002061
-
RNA sequencing reads
Dataset
EGAD00001004327
-
APL nanopore sequencing
Study
EGAS00001005618
-
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
-
CyclomicsSeq_IMCISION_Flongle
Dataset
EGAD00001010148
-
Real_time_ssRNAseq_flow_pilot
Study
EGAS00001006304
-
Epigenomic profile of diverse cancer
Study
EGAS00001004352
-
Paediatric Tumour Profiling
Study
EGAS00001003437
-
HCA_Heart_Adult_Wellcome_DNA
Study
EGAS00001006359
-
Genome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome
Study
EGAS00001006371
-
Finnish - THL Finrisk
Dataset
EGAD00001008580
-
ssCNV
Dataset
EGAD00001008997
-
SF10328
Dataset
EGAD00001008303
-
Lifelines-CH: processed somatic variant calls
Dataset
EGAD00001010144
-
Revision Experiments UMI
Dataset
EGAD00001010310
-
CyclomicsSeq_Healthy_Flongle
Dataset
EGAD00001010150
-
Sample sheet
Dataset
EGAD00001011166
-
Möebius
Dataset
EGAD00001001385
-
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001315
-
Integration of intra-sample contextual error modeling for improved detection of somatic mutations
Study
EGAS00001003806
-
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001314
-
Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001001316
-
Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC
Dac
EGAC00001003295
-
IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" Italian Cancer Center Data Access Committee
Dac
EGAC00001003223
-
IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" Italian Cancer Center Data Access Committee
Dac
EGAC00001003227
-
St. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee
Dac
EGAC00001000045
-
Sequencing component for the whole genome methylation analysis in PBMCs and cell subset pilot study DAC
Dac
EGAC00001000096
-
DEEP (Deutsches Epigenom Programm) DAC
Dac
EGAC00001000179
-
Department of Pathology and Tumor Biology, Kyoto University Data Access Committee
Dac
EGAC00001000352
-
The EMC-NICHE DAC considers appeals for hematopoietic/niche-related data sets.
Dac
EGAC00001000537
-
Data access policy for PDTX Breast Cancer data from Bruna et al (2016), Cell.
Dac
EGAC00001000540
-
CIR-RIMLS committee on data access to Immunological mechanisms for celiac disease database
Dac
EGAC00001000557
-
MSKCC Medical Donation Program Data Access Committee
Dac
EGAC00001000588
-
Data access committee for the pseudomyxoma peritonei exome sequencing vcf-files
Dac
EGAC00001000649
-
DAC for "A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors"
Dac
EGAC00001000675
-
DAC for Hungarian human exome team (Department of Medical Biology, University of Szeged, Hungary)
Dac
EGAC00001000838
-
Data access committee handling data access requests for biomarker data from the clinical trial IMvigor210.
Dac
EGAC00001000945
-
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness.
Dac
EGAC00001001054
-
DAC for study: "Circulating tumour DNA abundance and potential utility in de novo metastatic prostate cancer"
Dac
EGAC00001001099
-
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Dac
EGAC00001001138
-
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation Committee (part II)
Dac
EGAC00001001332
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Dac
EGAC00001001387
-
The University of Hong Kong Colon Cancer Organoids Genomics Study Data Access Committee
Dac
EGAC00001001405
-
Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC
Dac
EGAC00001001549
-
Data Access Committee - cfDNA fragmentation and personalized sequencing reveal ctDNA in urine and plasma of glioma patients
Dac
EGAC00001001593