-
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Study
EGAS00001004266
-
ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Study
EGAS00001006883
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT)
Study
phs001295
-
NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS
Study
phs000507
-
Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
Study
JGAS000052
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597
-
Genetic Epidemiology of COPD (COPDGene) Funded by the National Heart, Lung, and Blood Institute
Study
phs000179
-
National Institute of Dental and Craniofacial Research (NIDCR) Sjögren's International Collaborative Clinical Alliance (SICCA): Center for Inherited Disease Research (CIDR) Genome-Wide Genotyping
Study
phs000672
-
Therapeutic Trial of Potassium and Acetazolamide in Andersen-Tawil Syndrome
Study
phs001316
-
Assessing Neural Mechanisms of Injury in Inborn Errors of Urea Metabolism Using Structural MRI, Functional MRI, and Magnetic Resonance Spectroscopy
Study
phs001108
-
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Study
phs001591
-
Multiomic Landscape of Multiple Myeloma Precursor and Relapsed Disease
Study
phs003892
-
Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients
Study
EGAS00001001024
-
Whole Genome Sequence and RNASeq Samples for Lung Cancer
Study
EGAS00001007832
-
Benchmark and validation of whole exome sequencing of a trio and singleton for mobile element detection.
Dataset
EGAD00001000883
-
Genome-Wide Association Studies of Prematurity and Its Complications (African American)
Study
phs000353
-
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Study
phs001317
-
Ongoing Replication Stress Tolerance and Clonal T Cell Responses Distinguish Liver and Lung Recurrence and Patient Outcomes in Pancreatic Ductal Adenocarcinoma
Study
phs003597
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Gene expression profiling of SLE and healthy control samples
Study
EGAS00001005701
-
Bulk RNA-seq of Human Epiglottis and Subglottis
Dataset
EGAD50000001278
-
Single-nucleus RNA-sequencing of normal adrenal cortex and adrenocortical tumors
Dataset
EGAD50000000835
-
GBM cancer stem cell lines -RNA-seq and WGS data
Study
EGAS00001003700
-
Genomic characterization of pancreatic tumours and matched xenograft and organoid models - WGS mapped reads
Dataset
EGAD00001003586
-
Single cell and plasma RNA sequencing
Study
EGAS00001005194
-
Somatic SNVs and Indels for INSPIRE Tumor WES
Dataset
EGAD00001006569
-
DAC of "Gene expression adaptation of metastases to their host tissue"
Dac
EGAC50000000514
-
Scalable ultra-high-throughput multiplexed single-cell chromatin and RNA profiling reveals gene regulatory dynamics during stimulation time courses and CRISPR perturbation screens
Dac
EGAC50000000485
-
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Study
phs001672
-
RNA sequencing of skin tissue and peripheral blood mononuclear cells from patients with atopic dermatitis and healthy controls.
Study
JGAS000628
-
Total NF1 sequence in the patients with neurofaibromatosis type1
Study
JGAS000288
-
Data Access Committee for Maurice Lab - UMC Utrecht
Dac
EGAC50000000876
-
Waldenström Macroglobulinemia Single-Cell Data Access Committee
Dac
EGAC50000000863
-
TallFlow - multi-omics
Study
EGAS50000000358
-
Whole Exome Sequencing Data of indolent primary renal B-Cell lymphomas
Study
EGAS50000000774
-
SCANDARE HNSCC
Study
EGAS50000001158
-
Etiology of congenital thyroid dysfunction in Down Syndrome: a multi-omics investigation
Study
EGAS50000000264
-
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
Study
EGAS50000000303
-
snRNA-seq dataset and atlas from subcortical white matter MS lesions (CA & CI) and controls
Dataset
EGAD50000000521
-
DNA sequences from adolescent and young adult patients with melanoma treated with immunotherapy
Dataset
EGAD50000000353
-
NSCCG_CRC_GWAS
Dataset
EGAD00010002184
-
IMSGC and MultipleMS project MS patients from Germany, Mainz
Dataset
EGAD00010002484
-
IMSGC and MultipleMS project MS patients from Italy, Piedmont
Dataset
EGAD00010002490
-
IMSGC and MultipleMS project MS patients from Germany, TUM
Dataset
EGAD00010002489
-
IMSGC and MultipleMS project MS patients from Italy, OSR
Dataset
EGAD00010002486
-
SNP_array
Dataset
EGAD00010001667
-
Histone Acetylome-wide Association Study of Autism Spectrum Disorder
Study
EGAS00001001943
-
Single-cell T-cell receptor sequencing of intraepithelial gammadelta T-cells in celiac disease
Study
EGAS00001003897
-
Effect_of_FAM50_knockout_on_the_transcriptome
Study
EGAS00001004836