-
Genomics of acral lentiginous melanoma
Dataset
EGAD00001010126
-
Tagged-amplicon deep sequencing
Dataset
EGAD00001011058
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Dataset
EGAD00001011048
-
RNA-seq dataset: Single-cell spatial analysis of pediatric high-grade glioma reveals a novel population of immunosuppressive and tumor-promoting SPP1+/GPNMB+ myeloid cells
Dataset
EGAD00001015450
-
Transcriptional consequences of SETBP1 variants in developmental disorders and malignancies
Dataset
EGAD00001015482
-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
Personalized Medicine Strategy for MPNSTs: Using Precision Oncology on PDOX Models to Inform Tumor Boards
Study
EGAS50000001502
-
APOBEC mutagenesis is a common process in normal human small intestine
Dataset
EGAD00001008764
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk
Study
phs002566
-
Aurora US Metastatic Breast Cancer Retrospective Project
Study
phs002622
-
In vitro reconstitution of epigenetic reprogramming in the human germ line
Study
JGAS000690
-
Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Study
EGAS00001002443
-
Antisense long non-coding RNAs are deregulated in skin tissue of patients with systemic sclerosis
Study
EGAS00001002751
-
Similarity and diversity of the tumor microenvironment in multiple metastases: critical implications for overall and progression-free survival of high-grade serous ovarian cancer.
Study
EGAS00001002065
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
Study
EGAS00001002622
-
Liquid biopsy for molecular characterization of diffuse large B-cell lymphoma and early assessment of minimal residual disease
Study
EGAS50000000215
-
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
Study
EGAS50000000481
-
Raw sequencing files from WGS and RNA-Seq
Study
EGAS50000000186
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
The Cardiogenics study
Study
EGAS00001000411
-
Integrated analysis of relapsed B-cell precursor Acute Lymphoblastic Leukemia identifies subtype-specific cytokine and metabolic signatures
Study
EGAS00001002856
-
Intratumoural heterogeneity and immune modulation in lung adenocarcinoma of female smokers and never smokers
Study
EGAS00001006331
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
NOUS-209 off-the-shelf immunotherapy has the potential to hit primary and metachronous colorectal and urothelial cancer in Lynch syndrome
Study
EGAS50000001336
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
TSO500 STJAN33, BRAF mutated CUP
Dataset
EGAD50000000689
-
A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk
Dataset
EGAD50000000518
-
Gut 16S rRNA/FINRISK 2002
Dataset
EGAD50000000287
-
EGAD00010000282
Dataset
EGAD00010000282
-
Sequencing data for oesophageal and related samples - ICGC DCC release 27 earmarked (WGS)
Dataset
EGAD00001004028
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Dataset
EGAD00001001691
-
Analysis of the B cell receptor repertoire in six immune-mediated diseases
Dataset
EGAD00001005431
-
Single-cell gene expression data from CD8+ T cells from two Austrian COVID19 patients stimulated with wildtype and mutant SARS-Cov-2 peptides
Dataset
EGAD00001006995
-
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Dataset
EGAD00001007794
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Dataset
EGAD00001006888
-
Dataset for head_and_neck_cancer-EXON
Dataset
EGAD00001008880
-
Dataset for hepatopancreaticobiliary_malignancy-EXON
Dataset
EGAD00001008883
-
Dataset for hepatopancreaticobiliary_malignancy-WHOLE_GENOME
Dataset
EGAD00001008884
-
Dataset for neuroendocrine_adrenal_tumor-WHOLE_GENOME
Dataset
EGAD00001008893
-
Bulk RNA sequencing of Singapore colorectal cancer patients (SG-BULK)
Dataset
EGAD00001008512
-
Southern African Prostate Cancer Study (SAPCS) Ethnic Disparity
Dataset
EGAD00001009067
-
Upper cortical layer-driven network impairment in schizophrenia - 10x genomics v3 snRNA-seq and Visium spatial transcriptomics datasets
Dataset
EGAD00001009173
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Multiomic analysis of CD4+ T cells from blood, lymph node and tumor of NSCLC patients
Dataset
EGAD50000000424
-
Enrichment of Lung Microbiome with Supraglottic Taxa which is Associated with Increased Pulmonary Inflammation
Study
phs000633
-
Genomic Analysis of Pediatric Low Grade Gliomas
Study
phs000614
-
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Study
phs002653