-
RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
-
Single-cell multidimensional profiling of tumor cell heterogeneity in supratentorial ependymomas
Study
EGAS50000001513
-
Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
-
DynaTag for efficient profiling of transcription factors in small samples and single cells
Study
EGAS50000001074
-
Whole exome sequencing of bladder tumors
Study
EGAS50000001248
-
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
-
TDP43 proteinopathy leads to divergent cryptic splicing in the cortex and spinal cord
Study
EGAS50000000575
-
UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
-
Kidney_transplant_nephrectomy_scRNAseq
Study
EGAS00001003935
-
Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES
Study
EGAS00001005734
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination
Study
EGAS00001005816
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
PDAC organoid genomic heterogeneity
Study
EGAS00001006782
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Study
EGAS00001005461
-
Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome
Study
EGAS00001007079
-
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Study
EGAS00001007766
-
Data Quality Control
Documentation
access/request-data/quality-control-reports
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
Transcriptome sequencing of neuroendocrine tumors of the small intestine
Dataset
EGAD50000000906
-
Broad utility of ultrasensitive analysis of circulating tumor DNA (ctDNA) dynamics across solid tumors treated with immunotherapy
Dataset
EGAD50000001813
-
Mid-frequency hearing loss is a characteristic clinical feature of OTOA-associated hearing loss
Study
JGAS000200
-
CEITEC DAC
Dac
EGAC50000000049
-
Oral microbiota composition assessed with 16S rRNA sequencing from adults aged over 65 years old.
Dataset
EGAD00001007705
-
CRUK Accelerator: Non-small cell lung cancer whole exome and RNA sequencing
Dataset
EGAD00001007934
-
Amplicon-based sequencing of drug resistant lung cancer cell lines (2017-07-05)
Dataset
EGAD00001003425
-
Single-cell RNA-seq data of bronchoalveolar lavage fluid and extramedullary relapse of a multiple myeloma patient with sarcoidosis-like reactions after anti-BCMA CAR T-cell therapy
Dataset
EGAD00001008649
-
Comprehensive RNA repository of tissue and plasma from patients with esophageal cancer or precursor lesions
Dataset
EGAD00001006857
-
Ultra-deep sequencing of cell-free DNA derived from reference materials and a patient with asymmetric overgrowth
Dataset
EGAD00001009784
-
DNA-seq BAM files from 16 carriers of the BMPR2 p.Arg491Gln mutation in a family affected by HPAH
Dataset
EGAD00001005757
-
Hip OA Functional Genomics RNAseq (2017-06-09)
Dataset
EGAD00001003354
-
ENU-LS-411N-TripleTherapy
Dataset
EGAD00001002051
-
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Dataset
EGAD00001002067
-
microRNA-seq of human serum from a longitudinal study of 66 women with no history of cancer
Dataset
EGAD00001004348
-
Melanoma-Til Study RNAseq
Dataset
EGAD00001000325
-
Whole exome sequencing of young onset Primary Sclerosing Cholangitis
Dataset
EGAD00001000671
-
RNASeq_EGAS00001001306
Dataset
EGAD00001001443
-
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
Study
EGAS00001007339
-
Clinical and genetic analysis of a rare syndrome associated with neoteny
Study
EGAS00001002419
-
120 individuals from the TEENAGE study (Ntalla et al., 2013) have been genotyped on the Illumina HumanCoreExome-12v1-1_A array. This is a population-based study of adolescents from the Attica region in Greece
Study
EGAS00001001733
-
A Platform Study of Combination Immunotherapy for the Neoadjuvant and Adjuvant Treatment of Patients with Surgically Resectable Adenocarcinoma of the Pancreas
Study
phs003002
-
A Genome-Wide Association Comparative Analysis of Response of AF Patients to Rate Control Therapy; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000439
-
Genetic Analysis of the Chiari I Malformation
Study
phs001795
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs001088
-
Multicenter International Lymphangioleiomyomatosis Efficacy of Sirolimus Trial (The MILES Trial)
Study
phs000605
-
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Study
phs000433
-
National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci
Study
phs000168