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The Nordic Centre of Excellence Programme in Molecular Medicine Data Access Committee
Dac
EGAC00000000006
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005346
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Germany
Study
EGAS00001005858
-
A cycling, progenitor-like cell population at the root of atypical teratoid rhabdoid tumor subtype differentiation trajectories
Study
EGAS00001008123
-
Precise reconstruction of the tumor microenvironment using bulk RNA-seq and a unique machine learning-based algorithm trained on artificial transcriptomes
Study
EGAS00001006272
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005355
-
The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling
Study
EGAS00001006960
-
500FG DNA methylation data
Dataset
EGAD00010002769
-
Mexican_Biobank_Genotypes
Dataset
EGAD00010002361
-
EGAD00010000518
Dataset
EGAD00010000518
-
The UCSF Low Grade Glioma Genome Project #1
Dataset
EGAD00001000714
-
Datasets 929/938
Dataset
EGAD00001004457
-
Cell Line Dataset
Dataset
EGAD00001001349
-
Capture Hi-C
Dataset
EGAD00001001243
-
qDNAseq CLUC dataset
Dataset
EGAD00001002071
-
DAC monitoring the usage of ultra-low-coverage MinION nanopore sequencing results of NA12877 and NA12878 from NIGMS Human Genetic Cell Repository.
Dac
EGAC00001000876
-
Azienda Ospedaliero-Universitaria di Parma Data Accessibility
Dac
EGAC50000000239
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cambridge, UK
Study
EGAS00001005854
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Dublin, Ireland.
Study
EGAS00001005844
-
Whole Exome Sequencing of Bipolar cases and controls performed at the Broad Institute on a cohort from Cardiff, UK (Craddock)
Study
EGAS00001005845
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from London, UK
Study
EGAS00001005851
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Umea, Sweden.
Study
EGAS00001005842
-
Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease
Study
EGAS00001005348
-
PEVOsq WES data
Dataset
EGAD50000001013
-
preQC Genotypes
Dataset
EGAD00010002437
-
Gentoypes_SouthAfrica
Dataset
EGAD00010002467
-
GLASS-NL DNA-Methylation
Dataset
EGAD00010002647
-
EGA_PBC_phased
Dataset
EGAD00010001533
-
Determining the quality and complexity of NGS data without a reference genome
Dataset
EGAD00001000759
-
PEARL-CF Study
Dac
EGAC50000001012
-
BC WGS Dataset 3
Dataset
EGAD00001001351
-
BC WGS Dataset 4
Dataset
EGAD00001001353
-
Biomarker data
Dataset
EGAD00001009415
-
Mutational Landscape of Grey Zone Lymphoma
Study
EGAS00001004482
-
Prostate WGS data (early onset)
Dataset
EGAD00001003256
-
Prostate WGS data (late onset)
Dataset
EGAD00001003290
-
Japanese RIKEN liver cancer WGS
Dataset
EGAD00001001881
-
McGill EMC Community projects Release 7 for cell line "hTERT RPE1"
Dataset
EGAD00001007680
-
Whole-exome sequencing of glioblastomas with long-term relapse interval
Dataset
EGAD00001008568
-
Bulk ATAC-Seq HiSeq2500 v4 reagents (100M reads)
Dataset
EGAD00001010909
-
ChIP-seq bulk
Dataset
EGAD00001011136
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (Owen)
Study
EGAS00001005855
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Edinburgh, Scotland, UK.
Study
EGAS00001005843
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (O'Donovan)
Study
EGAS00001005852
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Landen, Stockholm, Sweden.
Study
EGAS00001005838
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Stockholm, Sweden (Pedersen)
Study
EGAS00001005856
-
Elucidating the heterogeneity of immunotherapy response and immune-related toxicities by longitudinal ctDNA and immune cell compartment tracking in lung cancer
Study
EGAS00001007291
-
Study2OrangeFiber
Dataset
EGAD00010002191
-
Study1PeaFiber
Dataset
EGAD00010002192
-
SolomonIslands.Dataset
Dataset
EGAD00010002306
-
SEAsia.Oceania.Australia
Dataset
EGAD00010002302
-
Present-day genomics from the Eurasian steppe
Dataset
EGAD00010001538
-
Bacteria Lateral sclerosis
Dataset
EGAD00001004458
-
Hessequa-descendants mitogenomes
Dataset
EGAD00001007676
-
Application of targeted long-read methylation sequencing to dissected breast cancer tissues
Study
JGAS000758
-
Building a Database of Genomic Structural Variants in Japanese population
Study
JGAS000580
-
_WGS__Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001004464
-
Neversmoker lung adenocarcinoma
Study
EGAS50000000232
-
Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer
Study
EGAS50000000284
-
Liquid-based genomic profiling in high-risk localized prostate cancer.
Study
EGAS50000001712
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
Partially methylated domains across multiple cell types
Study
EGAS00001003157
-
Whole Exome Sequencing of cohorts of Mutant Braf mouse model melanoma DNA and germline DNA.
Study
EGAS00001000729
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001003488
-
Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse
Study
EGAS00001005615
-
Multiregion Whole Exome and Smart-Seq3 single cell RNA sequencing of Breast Tumors
Study
EGAS00001006851
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
Genome and transcriptome sequence data from a colorectal adenocarcinoma patient (Response to Angiotensin Blockade with Irbesartan in a Patient with Metastatic Colorectal Cancer)
Dataset
EGAD00001001876
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Dataset
EGAD00001007502
-
Single-nucleus Transcriptome of Down Syndrome Brains (short-read)
Dataset
EGAD00001008287
-
Whole-exome sequencing laser capture micro-dissected biopsies of human renal cell carcinoma
Dataset
EGAD00001008029
-
Spatial transcriptome sequence data from HER2-positive human breast tumors (n=8, with 3 or 6 sections from each)
Dataset
EGAD00001008031
-
TK-EPN862 - Patient-derived xenograft model of Posterior Fossa A Ependymoma - RNAseq
Dataset
EGAD00001009870
-
IFN-γ and TNF-α drive a CXCL10+ CCL2+ Macrophage Phenotype Expanded in Severe COVID-19 Lungs and Inflammatory Diseases with Tissue Inflammation
Study
phs002780
-
Exome sequencing of samples taken at multipl time points to monitor therapy response in AML
Study
EGAS00001001948
-
hereditary BrEAst Case CONtrol study (BEACCON)
Dataset
EGAD00001007025
-
Data access committee (DAC) in the Graduate School of Medical Science and Engineering (GSMSE) at Korea Advanced Institute of Science and Technology (KAIST)
Dac
EGAC00001001643
-
DAC of The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals
Dac
EGAC00001002517
-
UTSW KCP DAC
Dac
EGAC50000000203
-
Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths
Study
EGAS00001007402
-
TSO500 on DNA
Dataset
EGAD50000000270
-
MiRNA_Validation
Dataset
EGAD00010002752
-
MiRNA_TrainTest
Dataset
EGAD00010002754
-
Gentoypes_Lesotho
Dataset
EGAD00010002468
-
Baka_saliva_450K
Dataset
EGAD00010001251
-
RNA Editing AZIN1 amplicon sequencing
Dataset
EGAD00001000708
-
Tracing the origins of relapse in AML to stem cells
Dataset
EGAD00001003234
-
IRF5 HL RNASeq dataset
Dataset
EGAD00001001417
-
Landscape of AL mutations
Dataset
EGAD00001001861
-
Exome sequencing Parkinson's disease patients
Dataset
EGAD00001000405
-
AI_NF1glioma_WES
Dataset
EGAD00001004375
-
ICR MOPOPGEN UK exome control series
Dataset
EGAD00001004396
-
Metadata file
Dataset
EGAD00001008792
-
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions
Study
EGAS50000000436
-
Genome and transcriptome sequence data from a metastatic adenocarcinoma of the lung patient
Dataset
EGAD00001004708
-
Genome and transcriptome sequence data from a adenocarcinoma of the liver patient
Dataset
EGAD00001004706
-
Genome and transcriptome sequence data from a metastatic squamous cell carcinoma of the esophagus patient
Dataset
EGAD00001005835
-
Genome and transcriptome sequence data from a metastatic squamous cell carcinoma of the lung patient
Dataset
EGAD00001005850
-
Genome and transcriptome sequence data from a metastatic cancer to the breast patient
Dataset
EGAD00001010959
-
Semmelweis University - Biophysics Data Access Committee
Dac
EGAC50000000053