-
Tandem DNA Repeats Activate hTERT Gene Transcription
Study
phs002428
-
Comprehensive gene analysis of colorectal cancer cases
Study
JGAS000128
-
Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins
Study
EGAS00001001240
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Androgen receptor blockade promotes response to BRAF/MEK-targeted therapy
Study
EGAS00001006196
-
Hexanucleotide repeat expansions in C9orf72 alter microglial responses and prevent a coordinated glial reaction in ALS
Study
EGAS00001006711
-
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis using bronchial specimens
Study
EGAS00001007089
-
Sample Multiplexing Oligo Comparison
Study
EGAS50000000153
-
Renal_Follow_Up_Series
Study
EGAS00001000095
-
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_Novaseq
Study
EGAS00001003433
-
National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease
Study
phs001172
-
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
Study
phs000239
-
C3 SNPs and outcome after lung transplantation
Study
EGAS00001003843
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Offspring Sex Impacts DNA Methylation and Gene Expression in Placentae from Women with Diabetes during Pregnancy
Study
phs001535
-
Rare germline sequence variants, copy number variations, expression alterations, methylation variations and disease susceptibility in familial melanoma
Study
phs001177
-
Genetics of Glucose Regulation in Gestation and Growth (Gen3G) Cohort - Placenta Transcriptomics RNA Sequencing
Study
phs003151
-
Cancer cell and tumor microenvironment biomarkers associated with disease-free survival with adjuvant nivolumab in the phase 3 CheckMate 274 trial
Study
EGAS50000000560
-
Relation between transcriptome, karyotype and age in cases of sex chromosome aneuploidies.
Study
EGAS50000001009
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - WGS data
Study
EGAS00001006610
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - Cancer Panel data
Study
EGAS00001006642
-
Relation between transcriptome, karyotype and age in cases of sex chromosome aneuploidies.
Study
EGAS00001007462
-
Research Study into The Molecular Genetics of Hereditary Neuropathies
Study
phs001351
-
Inherited Defect in ST6GalNAc1 Reveals Roles of Sialylation in Intestinal Homeostasis
Study
phs002598
-
Genomic and transcriptomic characterization of chordoma
Study
phs001643
-
Genomic Analysis of Bevacizumab-induced Hypertension
Study
phs001597
-
Genetic measurement of memory B-cell recall using antibody repertoire sequencing
Study
phs000656
-
Development of targeted DNA sequencing panel for brain tumors
Study
EGAS50000000699
-
RNA seq data of 2 lung cancer samples prepared using 2 different RNA-seq library preparation protocols
Study
EGAS50000001419
-
Clonal evolution of metastatic colorectal cancer under anticancer therapies
Study
EGAS50000001023
-
Targeted sequencing of breast cancers with germline BRCA1/2 mutations
Study
EGAS00001004182
-
Human_Colorectal_Cancer_Exome_Sequencing
Study
EGAS00001000077
-
RNASeq of PDX and CDX tumours treated with ADC
Study
EGAS00001004562
-
Whole Exome Sequencing of Calcitonin Producing Pancreatic Neuroendocrine Neoplasms (CT-pNENs) Indicates a Unique Molecular Signature
Study
phs003060
-
NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)
Study
phs001466
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Coronary Artery Risk Development in Young Adults Study (CARDIA)
Study
phs003045
-
Chromothripsis in human breast cancer (HIPO K26K/H017/A017)
Study
EGAS00001004662
-
Intratumoural heterogeneity and immune modulation in lung adenocarcinoma of female smokers and never smokers
Study
EGAS00001006331
-
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Dataset
EGAD00001000134
-
Long read whole genome sequencing data from brain postmortem tissue
Study
EGAS50000000921
-
Copy Number Variation using Affymetrix Optima Array
Study
EGAS00001006439
-
Single cell transcriptome atlas of immune cells in human small intestine and in Celiac disease
Dataset
EGAD00001005127
-
Geographic and age-related variations in mutational processes in colorectal cancer - patient metadata files (Mutographs)
Dataset
EGAD00001015437
-
Geographic and age-related variations in mutational processes in colorectal cancer - copy number variants (Mutographs)
Dataset
EGAD00001015487
-
Autosomal recessive CD70 deficiency is associated with combined immunodeficiency and EBV viremia
Study
phs001245
-
Alcohol Dependence: Sequencing from Multiplex Families
Study
phs001775
-
Genome-Wide Association Study of Lung Cancer Susceptibility in Never-Smoking Women in Asia
Study
phs000716
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
ABIS_1_MeDIP-seq
Study
EGAS00001001099
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Honolulu Heart Program (HHP-BioLINCC)
Study
phs003907
-
NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD)
Study
phs000366
-
Involvement of the FGF8/FGF Receptor Signaling Pathway in the Maintenance and Progression of Fusion-Positive Rhabdomyosarcoma
Study
phs004009
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
Histone chaperone CHAF1A promotes proliferation and tumorigenicity in gastric cancer and impacts prognosis via context-depedent regulation of gene expression
Study
EGAS00001003064
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations
Study
EGAS00001006034
-
Genomic Analysis of Peripheral T-Cell Lymphomas
Study
phs000689
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
The Multiomics Blueprint of the Individual with the Most Extreme Lifespan
Study
EGAS50000000884
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
single-stranded DNA study
Study
EGAS00001005093
-
Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation
Study
EGAS00001007237
-
Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study
Study
phs000383
-
Whole Genome Sequencing of Neuroblastoma
Study
EGAS00001000222
-
Molecular Characterization of Hemimegalencephaly
Study
phs002156
-
Genomic and Phenotypic Profile of Sickle Cell Disease in Human Population in Cameroon
Study
phs003748
-
Platelet RNAseq data for SLFN14 K219N patients
Study
EGAS00001006339
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
Exome Sequencing of Statin-Induced Myopathy Cases
Study
phs001342
-
Epi_Tax_targeted_sequencing
Study
EGAS00001000587
-
RNA-Seq datasets in human islets cultured in high glucose conditions
Dataset
EGAD00001005207
-
A Pilot Study Using Next Generation Sequencing in Advanced Cancers: Feasibility and Challenges
Study
phs000657
-
A comprehensive genetic map of cytokine responses in Lyme borreliosis
Study
EGAS50000000024
-
Copy number profile of ctDNA in ovarian cancer patients
Study
EGAS00001008226
-
Presence of bacterial infection in brains of patients with Huntington's disease (HD)
Study
EGAS00001003678
-
GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Study
EGAS00001002477
-
Single-cell T-cell receptor sequencing of intraepithelial gammadelta T-cells in celiac disease
Study
EGAS00001003897
-
Presence of bacterial infection in brains of patients with Parkinson's disease (PD)
Study
EGAS00001003643
-
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Study
phs001246
-
Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases in the Czech Republic
Dataset
EGAD50000000640
-
DAC for "Transcriptome analysis of human iPSC-derived microglia in a novel human 3D cortical tissue model"
Dac
EGAC50000000303
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
VRK3 depletion in Pontine Diffuse Midline Glioma DMG-K27 altered cells
Dataset
EGAD00001010097
-
Variant Calling used in ABB project
Dataset
EGAD00001004132
-
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Dataset
EGAD00001005950
-
TREM2+ Cells in Human Basal Cell Carcinomas
Study
phs003242
-
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Dataset
EGAD00001009740
-
The role of the mammalian SWI/SNF chromatin remodeling complex in neuroendocrine prostate cancer
Study
EGAS00001004177
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.
Study
EGAS00001004671
-
TCR β-chain repertoire characterization of regulatory and conventional T cells in peripheral blood from breast cancer patients and healthy individuals.
Study
EGAS00001002699
-
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Study
EGAS00001005981