-
Controlling cell differentiation with precision through understanding the structure and dynamics of gene regulatory networks
Study
JGAS000121
-
Genomics characterization of primary central nervous system lymphoma
Study
JGAS000021
-
Establishment of xenogfafts and cultured cell lines from clinical samples
Study
JGAS000585
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Study
EGAS50000001328
-
Co-culture experiment (hashed samples)
Study
EGAS50000001252
-
Multimodal epigenetic sequencing analysis of cell-free DNA identifies biomarkers for ALS diagnosis and progression
Study
EGAS50000001267
-
TenK10K Phase 1: Single Cell
Study
EGAS50000001653
-
Long-read sequencing of saliva collected and stablized at room temperature in Oragene devices on the PacBio Revio
Study
EGAS50000001666
-
Raw human sequencing data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Study
EGAS50000001517
-
Genetic landscape of pediatric Retinoblastoma
Study
EGAS00001000346
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
Exome sequencing of samples taken at multipl time points to monitor therapy response in AML
Study
EGAS00001001948
-
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia
Study
EGAS00001001847
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
-
TRACERx: TRAcking non-small cell lung Cancer Evolution through therapy (Rx). Pilot Study. Multi-region sequencing of early-stage NSCLCs.
Study
EGAS00001000809
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Study
EGAS00001002248
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03
Study
EGAS00001002851
-
Whole genome characterisation of lung cancer organoids and tissue
Study
EGAS00001002899
-
Study the differences at the trascriptome level between iNKT and T cells
Study
EGAS00001003176
-
Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation
Study
EGAS00001000563
-
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Study
EGAS00001000840
-
Whole Genome Sequencing to track subclonal heterogeneity in 18 samples from 3 Chronic Lymphocytic Leukemia patients subjected to repeated cycles of therapy.
Study
EGAS00001000885
-
Splicing patterns in SF3B1 mutated uveal melanoma generate shared immunogenic tumor-specific neo-epitopes
Study
EGAS00001005226
-
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors.
Study
EGAS00001002335
-
Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Study
EGAS00001002567
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
Combination_Immune_Checkpoint_Inhibition_in_Australian_Rare_Cancers_WES
Study
EGAS00001005709
-
Vento_Placental_Cell_Atlas
Study
EGAS00001004187
-
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Study
EGAS00001003184
-
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch05
Study
EGAS00001003285
-
Forty-Five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor
Study
EGAS00001003361
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Short and long-read sequencing of Brugada syndrome samples
Study
EGAS00001004927
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
Genomic profiling of localized (lFL) and systemic follicular lymphoma (sFL) reveals novel insights into FL pathogenesis
Study
EGAS00001006927
-
Single cell multi-omic study of H3-K27M mutant diffuse midline glioma across age and location
Study
EGAS00001006994
-
Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors
Study
EGAS00001007550
-
Colorectal Microenvironment Spatial Mapping
Study
EGAS00001008254
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Breast cohort
Dataset
EGAD00001006293
-
Diverse mutational landscapes in human lymphocytes
Dataset
EGAD00001008107
-
Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer
Dataset
EGAD00001009863
-
Tracking the evolution of esophageal squamous cell carcinoma under dynamic immune selection by multi-omics sequencing
Dataset
EGAD00001009482
-
A DNA methylation atlas of normal human cell types
Dataset
EGAD00001009789
-
A Tumour Organoid Biobank for Mapping Cancer Cell Vulnerabilities - WGS
Dataset
EGAD00001015469
-
A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genes
Study
phs003348
-
High-Risk Breast Cancer GWAS
Study
phs000929
-
GSA bigbatch raw data
Dataset
EGAD00010002569
-
GSA pilot raw data
Dataset
EGAD00010002567
-
Data Access Committee of CiRA Foundation
Dac
EGAC50000000128
-
Genomic characterization of a patient with AGS and CdLS transcriptomic comparison of his monocytes against healthy and disease control samples
Study
EGAS00001007829
-
10X single cell RNA- and feature barcode sequencing of 38 AML samples
Dataset
EGAD50000001577
-
DFCI Gynecological Oncology Data Access Committee
Dac
EGAC50000000712
-
scRNA dataset for 15 samples
Dataset
EGAD50000001424
-
RNA sequencing of Notch inhibitor treated HCC PDX models across timepoints
Dataset
EGAD50000000737
-
Bulk RNA-sequencing datasets from Caco-2 cells under normal or inflamed conditions treated with 4HTBZ or vehicle.
Dataset
EGAD50000001759
-
Single Cell Multiome ATAC + Gene Expression sequencing
Dataset
EGAD50000001515
-
PRO-SPeCT: PROstate cancer heterogeneity deconvolution through Single cell Profiling of Chromatin accessibility and Transcriptomic output
Dataset
EGAD50000000745
-
scRNA transcriptome and TCR sequencing data modeling treatment responses in eight renal cell carcinoma patient
Dataset
EGAD50000001934
-
A single-cell atlas of the early COPD lung - Nanopore long-read
Dataset
EGAD50000001002
-
EM-seq data from plasma cfDNA samples of ALS patients, control and C9-carriers
Dataset
EGAD50000001808
-
Common origin and somatic mutation patterns of composite lymphomas and leukemias
Dataset
EGAD50000001486
-
Single Cell RNASeq for ARMS tumors
Dataset
EGAD50000002241
-
Genomic Variant Dataset of 5,309 Jeju Residents: Integrated WGS and SNP Array Analysis
Dataset
EGAD50000002451
-
Variant calling for LUNG-NSCLC2 cohort
Dataset
EGAD50000002235
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (ChIP-Seq for CD14-positive, CD16-negative classical monocyte, on genome GRCh37)
Dataset
EGAD00001002672
-
Test dataset with ligh-weight files
Dataset
EGAD00001009826
-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Dataset
EGAD00001005356
-
BRCA2, ATM, and CDK12 defects differentially shape prostate tumor driver genomics and clinical aggression
Dataset
EGAD00001006733
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Dataset
EGAD00001006796
-
MutWP5: CRUK Mutographs of Cancer: Breast: BRCA Carriers (Exome) (2020-01-29)
Dataset
EGAD00001005921
-
MutWP5: CRUK Mutographs of Cancer: Breast: Cancer Mastectomy (Targeted) (2020-01-29)
Dataset
EGAD00001005923
-
Targeted Germline Sequencing of the Leeds Melanoma Cohort
Dataset
EGAD00001007520
-
Whole Exome Sequencing data of glioma from the Chinese Glioma Genome Atlas (CGGA) project
Dataset
EGAD00001006445
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (ChIP-Seq for CD4-positive, alpha-beta T cell, on genome GRCh37)
Dataset
EGAD00001002673
-
Genetic regulation of RNA splicing in human pancreatic islets
Dataset
EGAD00001009102
-
scRNA-seq dataset of patient and healthy donors
Dataset
EGAD00001008372
-
Cell-free DNA and bone marrow samples from myelodysplastic syndromes
Dataset
EGAD00001008567
-
WGS of tissues from members of family with germline POLD1 L474P variant
Dataset
EGAD00001009282
-
T cell transcriptional gradient
Dataset
EGAD00001009677
-
Whole-genome plasma DNA sequencing in CRC patients under anti-EGFR therapy
Dataset
EGAD00001000748
-
H3K27ac/H3K27me3 landscape of medulloblastoma
Dataset
EGAD00001009709
-
MutWP5: CRUK Mutographs of Cancer: Breast: BRCA Carriers (Targeted) (2020-01-29)
Dataset
EGAD00001005920
-
High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder
Dataset
EGAD00001004082
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (RNA-Seq for CD14-positive, CD16-negative classical monocyte, on genome GRCh37)
Dataset
EGAD00001002674
-
The British Autozygosity Populations BioResource (2018-06-06)
Dataset
EGAD00001004150
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Dataset
EGAD00001003783
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Dataset
EGAD00001006797
-
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
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002697