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T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Assessing mitochondrial bioenergetics in coronary artery disease: A translational left ventricular tissue study in humans (The AMBITION study).
Study
EGAS00001007351
-
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
-
Spatio-temporal Profiling of a Rhabdoid Tumor Case Study
Study
EGAS00001008174
-
Epigenetic age deceleration reflects fitness improvements following a six-month endurance exercise intervention
Study
EGAS00001008221
-
Whole exome sequencing data for paired non-serous endometrial and ovarian carcinomas from 27 patients with concurrent tumours.
Study
EGAS00001008259
-
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
-
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
-
Genome-wide cell-free DNA termini in patients with cancer
Study
EGAS00001005738
-
Genome-wide cell-free DNA termini in patients with cancer
Study
EGAS00001005747
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Study
EGAS00001006879
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Genome-wide association study identifies common variants associated with breast cancer in South African Black women
Study
EGAS00001008032
-
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
-
Single cell RNA-seq mapping of nasal and tracheobronchial airways in human healthy volunteers
Study
EGAS00001004082