-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
Spatial Dynamics of the Developing Human Heart
Study
EGAS50000001122
-
HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Study
EGAS00001004723
-
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Study
EGAS00001002612
-
Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer
Study
EGAS50000000297
-
Peripheral blood DNA methylation and transcriptomics of vedolizumab and ustekinumab treatment response in patients with Crohn's disease
Study
EGAS50000000263
-
SeqControl: Process Control for DNA Sequencing
Study
EGAS00001000899
-
Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing
Study
EGAS00001001736
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
Using de novo assembly to identify structural variation of complex immune system gene regions
Study
EGAS00001005046
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
ARHGAP11A Maintains Cortical Progenitor Identity Through RHOA–ROCK Signalling During Human Brain Development
Study
EGAS00001008322
-
Centers for AIDS Research (CFAR) Network of Integrated Clinical Systems (CNICS)
Study
phs001788
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899
-
Multi-Ethnic Study of Atherosclerosis (Electrocardiogram Tracing Repository)
Study
phs003703
-
Cancer-Restricted Cryptic Antigens Are Targets for T Cell Recognition
Study
phs003887
-
Host-microbe interactions in a novel SARS-CoV-2 human challenge model
Study
EGAS50000001440
-
Identification of putative multiple myeloma (MM) susceptibility genes
Study
EGAS50000001259
-
A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy
Study
EGAS50000000228
-
A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Dataset
EGAD50000001712
-
Tamoxifen Response at Single Cell Resolution in Estrogen Receptor Positive Primary Human Breast Tumors
Study
phs003186
-
Prospective Procurement of Solid Tumor Tissue to Identify Novel Therapeutic Targets
Study
phs001003
-
Reference Profiles of ExRNAs in Normal Human Pregnancy
Study
phs003182
-
Single Cell Analysis Reveals Immune Dysfunction from the Earliest Stages of CLL that can be Reversed by Ibrutinib
Study
phs002705
-
Correlates of Human Nerve Repair
Study
phs001796
-
Epigenetic Damage in Women Living in LA Food-Desert Zip Codes
Study
phs003522
-
Elucidation of the association between viruses and autoimmune diseases and COVID-19
Study
JGAS000741
-
Analytical study of protein function and RNA expression involved in predicting treatment efficacy and adverse event development in lung cancer radiotherapy.
Study
JGAS000545
-
RNaseq of mantle cell lymphoma patient samples
Study
EGAS50000001086
-
Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes
Study
EGAS00001004165
-
Genomic landscape of aplastic anemia
Study
EGAS50000001516
-
Intratumor heterogeneity evaluation in primary HCC cells
Study
EGAS00001001135
-
Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans
Study
EGAS00001002736
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
scRNA-seq of total bone marrow mononuclear cells and CD3+ T cells of multiple myeloma patients and healthy donors
Study
EGAS00001006980
-
Neoantigen Landscape in a Hypermutated Glioblastoma Arising in a Patient with Germline POLE Deficiency Treated with Checkpoint Blockade Immunotherapy
Study
phs001663
-
Genome sequencing of biliary tract cancers
Study
JGAS000109
-
Genome sequencing of biliary tract cancers
Study
JGAS000389
-
CHEK2 molecular manuscript
Study
EGAS50000000080
-
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Study
EGAS00001000878
-
ScDNAseq in pediatric UBA1-mutated MDS
Study
EGAS50000001651
-
Mutation_burden_in_sun_exposed_eyelid__MSSE_
Study
EGAS00001002512
-
Whole genome sequencing of Japanese HCCs
Study
EGAS00001000671
-
Partially methylated domains across multiple cell types
Study
EGAS00001003157
-
Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Study
EGAS00001002626
-
Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients
Study
EGAS00001004413
-
Dac for "Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype"
Dac
EGAC50000000168
-
Single-cell RNA-sequencing for peripheral blood mononuclear cells and plasma proteomics data from COVID-19 patients and healthy controls of Japanese
Study
JGAS000783
-
ATAC-seq, H3K27ac CUT&Tag, and UMI-4C in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Study
EGAS50000000499
-
H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers
Study
EGAS00001006645
-
Whole genome and RNAseq analysis of pediatric osteosarcoma
Study
EGAS00001003201
-
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Study
phs001359
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Study
phs002094
-
Influence of age on molecular changes and treatment stratification in multimodal glioblastoma therapy
Study
EGAS00001008246
-
Bone marrow breakout lesions act as key sites for tumor-immune cell diversification and exhaustion in multiple myeloma
Study
EGAS50000000304
-
Monocyte and macrophage lipid accumulation results in downregulated type-I interferon responses
Study
EGAS00001005955
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
Chronic Renal Insufficiency Cohort (CRIC) Study Metabolomics and Proteomics
Study
phs003709
-
Mind Body Study: A Sub-Study on Psychosocial Factors and Microbiomes of Nurses in the Nurse's Health Study II
Study
phs003786
-
Establishing stable brain tumor stem cell lines and translational research for new treatments
Study
JGAS000657
-
DynaTag for efficient profiling of transcription factors in small samples and single cells
Study
EGAS50000001074
-
TDP43 proteinopathy leads to divergent cryptic splicing in the cortex and spinal cord
Study
EGAS50000000575
-
ARAF Mutations Confer Resistance to RAF Dimer Inhibitor Belvarafenib in NRAS- and BRAF- Mutant Melanoma
Study
EGAS00001005086
-
Investigating Genetics of Human Natural Short Sleepers (IGHNSS)
Study
phs001270
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
Gene Environment Association Studies (GENEVA): Genetics of Early Onset Stroke (GEOS) Study
Study
phs000292
-
Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older
Study
phs000287
-
OurHealth - Cardiovascular Disease in South Asians
Study
phs003821
-
McGill Epigenomics Mapping Centre
Study
EGAS00001000995
-
Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
HCA_Skin_Disease_WSSS_Spatial_NCL
Study
EGAS00001005278
-
HLA sequence data and final calls for VaccGene and 1000Gp3 African populations
Dataset
EGAD00001011379
-
Coronary Artery Risk Development in Young Adults (CARDIA-BioLINCC)
Study
phs003739
-
FEGA and European GDI: working together to improve human health
Blog
fega-and-gdi
-
Effects of tobacco smoking on the tumor immune microenvironment in head and neck squamous cell carcinoma
Study
phs001994
-
Genetics of Pigmentation in Eastern and Southern African Populations Study
Study
phs001396
-
Maternal-Fetal Immune Responses in Preterm Labor and Congenital Anomalies
Study
phs001693
-
Genomic and ecologic characteristics of the airway microbial-mucosal complex
Study
EGAS00001006689
-
Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome
Study
EGAS00001006982
-
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Study
EGAS00001003981
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk
Study
phs002566
-
Children's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study
Study
phs000199
-
Genetic Markers of Caries Risk in Diverse Underserved Children: CIDR
Study
phs003280
-
Collection: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Study
phs003650
-
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
Study
EGAS50000000481
-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686
-
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Study
phs000684
-
Mayo-Perlegen LEAPS (Linked Efforts to Accelerate Parkinson's Solutions) Collaboration
Study
phs000048
-
NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes
Study
phs000518
-
Plasma MicroRNA Signatures of Aging
Study
EGAS00001008117
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
Genomic and Transcriptomic Landscape of Fibrolamellar Hepatocellular Carcinoma
Study
phs000709
-
Inherited T Cell Defects: Diagnosis, Mechanisms and Treatments
Study
phs002968
-
Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi
Study
phs001320
-
Single-Cell Sequencing of Genomic DNA, RNA, and ADT in CRISPR-Edited Cells
Study
phs004042