-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Study
EGAS00001005053
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Study
EGAS00001005098
-
tFL with a PMBL GE signature
Study
EGAS00001005870
-
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Study
EGAS00001004455
-
Human liver NPCs single cell project
Study
EGAS00001007194
-
The Dutch Microbiome Project Batch 2
Dataset
EGAD00001007501
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
Convergent somatic mutations in effectors of insulin signalling in chronic liver disease
Dataset
EGAD00001006255
-
Precise reconstruction of the tumor microenvironment using bulk RNA-seq and a unique machine learning-based algorithm trained on artificial transcriptomes
Dataset
EGAD00001008776
-
UCSF Pediatric Bithalamic Glioma Genome Project
Dataset
EGAD00001005499
-
The scRNA dataset for TIGIT in MCL with CART
Dataset
EGAD00001010180
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Dataset
EGAD00001011048
-
Tagged-amplicon deep sequencing
Dataset
EGAD00001011058
-
Genomics of acral lentiginous melanoma
Dataset
EGAD00001010126
-
Dataset for urologic_cancer-RNA
Dataset
EGAD00001008851
-
Dataset for soft_tissue_tumor-EXON
Dataset
EGAD00001008897
-
RNAseq from blood CD34+ cells
Dataset
EGAD00001008194
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015455
-
RNA-sequencing of ex vivo exhausted human antigen-specific T cells
Dataset
EGAD00001009754
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Transcriptional consequences of SETBP1 variants in developmental disorders and malignancies
Dataset
EGAD00001015482
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015457
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015456
-
Sebaceous carcinoma tumor/normal exome sequencing and transcriptome sequencing. Transcriptome sequencing of
Dataset
EGAD00001004016
-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
APOBEC mutagenesis is a common process in normal human small intestine
Dataset
EGAD00001008764
-
Personalized Medicine Strategy for MPNSTs: Using Precision Oncology on PDOX Models to Inform Tumor Boards
Study
EGAS50000001502
-
Liquid biopsy for molecular characterization of diffuse large B-cell lymphoma and early assessment of minimal residual disease
Study
EGAS50000000215
-
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
-
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
Study
EGAS50000000481
-
Raw sequencing files from WGS and RNA-Seq
Study
EGAS50000000186
-
In vitro reconstitution of epigenetic reprogramming in the human germ line
Study
JGAS000690
-
The Cardiogenics study
Study
EGAS00001000411
-
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
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
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
-
Gut 16S rRNA/FINRISK 2002
Dataset
EGAD50000000287
-
A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk
Dataset
EGAD50000000518
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
NOUS-209 off-the-shelf immunotherapy has the potential to hit primary and metachronous colorectal and urothelial cancer in Lynch syndrome
Study
EGAS50000001336
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400