-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study
Study
phs001398
-
Single Cell Analysis of Psoriasis Resolution following IL-23 Blockade
Study
phs003351
-
HiDEF-seq single-molecule sequencing of single-strand mismatches and damage
Study
EGAS50000000318
-
Whole Exome and RNA Sequencing of 22 Patient-Derived Xenografts from Estrogen Receptor-Positive Breast Cancers
Study
phs003324
-
A Phase II Study: CRS207/GVAX Plus Anti-PD1 and Anti-CTLA4 Recruits Mesothelin- and KRAS-Specific T cells into PDAC
Study
phs003798
-
Impact of cryopreservation on transcriptome analysis of peripheral blood mononuclear cells
Study
EGAS50000001196
-
Lessons learned from the exome sequencing of nine cases of infertility and the way forward
Study
EGAS50000001320
-
bulk RNAseq analysis of tumor from 3 non-muscle-invasive bladder cancer patients
Study
EGAS50000001383
-
Proteogenomic discovery of a novel class of cancer antigens by HLA ligandome analysis of colon cancer tissues
Study
JGAS000280
-
Whole genome sequencing data of paediatric patients with BCR::ABL1 acute lymphoblastic leukemia
Study
EGAS50000001512
-
A human induced pluripotent stem cell toolbox for studying sex chromosome effects -transcriptional landscape
Study
EGAS50000000931
-
Genome-wide evaluation of the maturation of the immune response to the tuberculin skin test from day 2 to day 7
Study
EGAS50000000822
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
ICGC Oesophageal adenocarcinoma - pilot samples
Study
EGAS00001000559
-
Identification_of_drug_resistance_genes_in_melanoma
Study
EGAS00001000617
-
Single-cell RNA-sequencing of CD34+ bone marrow cells from patients with SLE, healthy individuals and umbilical cord blood samples
Study
EGAS00001007317
-
Comprehensive analysis of the (epi)genome of pediatric atypical teratoid/rhabdoid tumours (AT/RTs)
Study
EGAS00001001297
-
ICGC Oesophageal adenocarcinoma - Barrett's samples
Study
EGAS00001000726
-
Multiregion Whole Exome sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001001436
-
Somatic point mutation data from microsatellite unstable colorectal cancers
Study
EGAS00001003101
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
RNA sequencing of undifferentiated sarcomas
Study
EGAS00001003291
-
Tumor microenvironment study of ovarian granulosa cell tumors
Study
EGAS00001006478
-
T cell reactivity of MHC epitopes
Study
EGAS00001006445
-
Identification and functional characterisation of a rare MTTP variant underlying familial non-alcoholic fatty liver disease
Study
EGAS00001005254
-
Duplexseq of the interstrand crosslinks_WGS
Dataset
EGAD00001010298
-
University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders)
Study
phs000436
-
Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Global Alliance to Prevent Prematurity and Stillbirth (GAPPS)
Study
phs003620
-
Resuscitation Outcomes Consortium (ROC) Trauma Epidemiologic Registry (Trauma Epistry) (ROC-Trauma Epistry-BioLINCC)
Study
phs003809
-
HeartShare - Extant Datasets - Harmonized Clinical Trials Collection
Study
phs003989
-
Transcriptomic analysis of liver CD8+ T cells
Study
EGAS00001006885
-
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Study
EGAS00000000056
-
Study of Adaptation to Hypoxia in Ethiopian Highlanders via Whole Genome Sequencing
Study
phs000647
-
IFN-γ and TNF-α drive a CXCL10+ CCL2+ Macrophage Phenotype Expanded in Severe COVID-19 Lungs and Inflammatory Diseases with Tissue Inflammation
Study
phs002780
-
Transcriptome of 2-Hydroxypropyl-Beta-Cyclodextrin Treatment in Niemann-Pick Disease Type C1
Study
phs002392
-
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Study
phs000678
-
University of Texas at Austin (UTA) Histone Modification and Gene Expression Profiling in 9 Primary Glioblastoma Multiforme, 2 Anaplastic Astrocytomas and Two Meningiomas
Study
phs001389
-
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
Study
phs001846
-
Methylation-Based Immune Deconvolution in Prostate Cancer Patients Before and After Radical Prostatectomy
Study
phs003660
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program - Neuroblastoma
Study
phs003163
-
Human papillomavirus integration induces oncogenic host gene fusions in oropharyngeal cancers
Study
EGAS50000000892
-
Epigenomics of Neurocognitive Function in Breast Cancer
Study
phs003959
-
Longitudinal single-cell transcriptomic study in patient-derived xenografts of pediatric T-ALL
Study
EGAS50000000582
-
Clonal Evolution and Transcriptional Plasticity Shape Metastatic Dissemination Routes in Prostate Cancer
Study
EGAS50000000927
-
APOL1 Risk Variants Induce Metabolic Reprogramming of Podocytes in Patient-Derived Kidney Organoids
Study
EGAS50000001223
-
Analysis of the co-occurrence of LOY and CHIP in Alzheimer's disease patients and control individuals using whole-exome sequencing (WES)
Study
EGAS00001008234
-
H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent.
Study
EGAS00001002976
-
Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors
Study
EGAS00001007877
-
Transcriptome Changes in ASD (NRXN1α+/-) iPSC-derived neurons
Study
EGAS00001005536
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Study
EGAS00001000400
-
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML
Study
EGAS00001003820
-
Conserved interferon-gamma signaling and decreased immune exclusion programs in responses to immune checkpoint blockade therapy
Study
EGAS00001004545
-
Reprogramming of stroma-derived chemokine networks drives the loss of tissue organization in nodal B cell lymphoma
Study
EGAS00001006986
-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Dataset
EGAD00001011349
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Breast cohort
Dataset
EGAD00001006293
-
Characterisation of the genomic landscape of CRLF2-d ALL
Dataset
EGAD00001002008
-
Characterisation of the genomic landscape of CRLF2-d ALL
Dataset
EGAD00001002007
-
ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer
Study
phs001221
-
Multiple Myeloma Genomic Study (MMGS)
Study
phs001323
-
PAK4 inhibition improves PD-1 blockade immunotherapy
Study
phs001919
-
T2D-GENES Project 2: San Antonio Mexican American Family Studies
Study
phs000462
-
Molecular characterization of invasive lobular carcinoma
Dataset
EGAD00001000288
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
Rare Disease Susceptibility Variant Study in Children with Crohn's Disease and Their Parents Using Targeted Gene Sequencing.
Study
phs001751
-
Whole Exome and Transcriptome Sequencing in Sporadic ALS
Study
phs000747
-
Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas
Study
phs002380
-
High response rate to anti PD-1 therapy in desmoplastic melanoma
Study
phs001469
-
Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure
Study
phs001501
-
Clinical Resistance to Crenolanib in Acute Myeloid Leukemia Due to Diverse Molecular Mechanisms
Study
phs001628
-
Methotrexate Clearance GWAS in Acute Lymphoblastic Leukemia (ALL) Patients
Study
phs000637
-
Efficacy of Bitter Taste Blockers on Flavor Acceptance in a Human Population
Study
phs000839
-
Genomic Analysis of Prostate Tumor Heterogeneity in Metastasis
Study
phs003404
-
Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases
Study
phs003005
-
HuBMAP: Single-Cell Multiplex Chromatin and RNA Interactions in Aging Human Brain
Study
phs003568
-
Programs, Origins, and Immunomodulatory Functions of Myeloid Cells in Gliomas
Study
phs003756
-
M116 Proteome Extracellular Vesicle Profiling
Dataset
EGAD50000001679
-
Adaptive Therapy Exploits Fitness Deficits in Chemotherapy-Resistant Ovarian Cancer to Achieve Long-Term Tumor Control Open Access
Study
EGAS50000001142
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
-
Changes in alternative splicing and associated neo-antigens due to therapy
Study
EGAS00001004524
-
An Atlas of Cells in the Human Tonsil
Study
EGAS00001006375
-
CM067 WES - Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Dataset
EGAD00001007573
-
Sleep Heart Health Study (SHHS-BioLINCC)
Study
phs003637
-
Multimodal Immune Profiling to Determine Mechanisms of COVID-19 Clinical Trajectory in Uganda
Study
phs003246
-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
Biomarkers in Transplant Recipients
Study
phs000960
-
Expression of Activation Induced Cytidine Deaminase and Risk of Transformation in Follicular Lymphoma
Study
phs002845
-
Extent and Significance of Bacterial DNA Integrations in the Human Cancer Genome
Study
phs001936
-
Single Cell RNA-Seq Reveals Malignant and Stromal Programs Associated with Metastasis in Head and Neck Cancer
Study
phs001474
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Study
EGAS00001003661
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Whole Tumor spatial heterogeneity in metastatic melanoma
Study
EGAS00001003292
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586