-
Genome of the Netherlands
Study
EGAS00001000644
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Study
EGAS00001002117
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Tissue-specific mutation accumulation in human adult stem cells during life
Study
EGAS00001001682
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Study
EGAS00001007573
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Study
EGAS00001002272
-
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
-
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples
Study
EGAS00001002631
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
Whole genome study of Hurthle cell thyroid carcinoma
Study
EGAS00001000940
-
H3.3G34R/V-transformed interneuron progenitors co-opt PDGFRA for gliomagenesis
Study
EGAS00001004301
-
The spatio-temporal evolution of lymph node spread in early breast cancer
Study
EGAS00001002947
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01
Study
EGAS00001000249
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
ICU_transcriptomics__Assessing_the_role_of_the_host_immune_response_in_patients_with_ventilator_associated_pneumonia
Study
EGAS00001003074
-
Whole Tumor spatial heterogeneity in metastatic melanoma
Study
EGAS00001003292
-
Exploiting evolutionary steering in cancer therapy
Study
EGAS00001003200
-
Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Study
EGAS00001003452
-
Genome-wide study of the effect of blood collection tubes on the cell-free DNA methylome
Study
EGAS00001004271
-
Long-read trio sequencing of unsolved patients with intellectual disability
Study
EGAS00001004319
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia
Study
EGAS00001001146
-
Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Study
EGAS00001004467
-
The clonal and mutational evolution spectrum of primary triple negative breast cancers
Study
EGAS00001000132
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Combining transcription factor binding affinities with open chromatin data for accurate gene expression prediction
Study
EGAS00001002073
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia
Study
EGAS00001003975
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia
Study
EGAS00001004325
-
Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Study
EGAS00001003964
-
Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Study
EGAS00001004538
-
Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells.
Study
EGAS00001002983
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235
-
DNA methylation analysis on PBL obtained from male patients with UC-PSC, UC and HC
Study
EGAS00001005832
-
Predictive value of chromosome 18q11.2-q12.1 loss for benefit from bevacizumab in metastatic colorectal cancer; a post-hoc analysis of the randomized controlled trial AGITG-MAX
Study
EGAS00001005453
-
A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma
Study
EGAS00001004709
-
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
-
A Dose Escalation Study of Efmarodocokin Alfa (UTTR1147A) in Healthy Volunteers and Patients with Ulcerative Colitis
Study
EGAS00001006172
-
Single_cell_characterization_of_T_cell_lymphoma_
Study
EGAS00001005750
-
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Study
EGAS00001003497
-
Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Study
EGAS00001006118
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Study
EGAS00001003973
-
Whole-genome sequencing of normal Singaporean volunteers
Study
EGAS00001004007
-
Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models: validation cohort
Study
EGAS00001006582
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Atypical B cells and impaired SARS-CoV-2 neutralisation following heterologous vaccination in the elderly
Study
EGAS00001007385
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Study
EGAS00001007555
-
Genome-wide association study identifies common variants associated with breast cancer in South African Black women
Study
EGAS00001008032
-
WGS and WES data of invasive micropapillary carcinoma of breast
Dataset
EGAD00001008450
-
cfMethyl-seq data (cfSort study) from serial plasma samples of NSCLC patients
Dataset
EGAD00001010881
-
The long term effects of chemotherapy on normal blood - WGS dataset
Dataset
EGAD00001015339
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
Osteosarcoma 3D patient derived cultures to test genome-informed personalized treatment options; a feasibility study
Study
EGAS50000001583
-
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
-
Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors
Study
EGAS00000000074
-
Further details about data access are available at KNIH DAC.
Dac
EGAC00001000487
-
Pharmacological improvement of CFTR function rescues airway epithelial homeostasis and host defense in cystic fibrosis children
Study
EGAS50000000128
-
Systemic Lupus Erythematosus Serum Stimulation of Human Intestinal Organoids Induces Barrier Leakiness and Changes in Goblet Cell Differentiation
Study
EGAS50000000012
-
Carboxylesterase 1 mediates a distinctive metabolic profile of dendritic cells to attain an inflammatory phenotype
Study
EGAS50000000230
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
Circulating tumor DNA dynamics reveal KRAS G12C mutation heterogeneity and response to treatment with the KRAS G12C inhibitor divarasib in solid tumors
Study
EGAS50000000315
-
Lactate metabolism in cancer stem cell fate regulation
Study
EGAS50000000063
-
Tumor Evolution Analysis Uncovered Immune-Escape Related Mutations in Relapsed Diffuse Large B-Cell Lymphoma
Study
EGAS50000000032
-
Surgery in combination with immune checkpoint therapy as an effective treatment for patients with metastatic cancer.
Study
EGAS00001005667
-
Impact of Glycolysis Inhibition on the Epigenome of Synovial Fluid T Cells in Juvenile Idiopathic Arthritis
Study
EGAS50000000808
-
Circulating Tumor DNA Analysis in ERBB2-Amplified Colorectal Cancer: Biomarker Analysis of the MyPathway Trial
Study
EGAS50000000916
-
Nanopore sequencing of blood, saliva, buccal mucosa samples of patients with inherited retinal disorders
Study
EGAS50000000440
-
PCR-free shallow whole genome sequencing for chromosomal copy number detection from plasma of cancer patients is an efficient alternative to the conventional PCR-based approach
Study
EGAS00001004692
-
Coding and regulatory somatic profiling of triple-negative breast cancer in Sub-Saharan African patients
Study
EGAS50000001013
-
Whole-genome and transcriptome versus panel sequencing in precision oncology: A translational-clinical comparison
Study
EGAS50000000431
-
Mutational signatures in normal tissues of patients treated with clinical stage G-quadruplex binder CX5461
Study
EGAS50000001145
-
Transcriptome profiling of megakaryocytes and platelets: application to GP9- and IKZF5-related thrombocytopenia
Study
EGAS50000001276
-
Complex genotype-phenotype relationships shape the response to treatment of Down Syndrome Childhood Acute Lymphoblastic Leukaemia
Study
EGAS50000001287
-
Heterogeneity of IKZF1 genomic alterations and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS50000000106
-
Case Report: Pre-Clinical Combination Targeting VEGF and PI3K in a Rare, Aggressive Mixed Endometrial Carcinoma
Study
EGAS50000001665
-
An autoinflammatory RIG-I variant causing Singleton-Merten Syndrome associates with small non-coding Y-RNAs
Study
EGAS50000001660
-
Sequencing and analysis of a South Asian-Indian personal genome
Study
EGAS00001000328
-
Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing
Study
EGAS00001000850
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001585
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001598
-
Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoids
Study
EGAS00001008227