-
Single-cell RNA sequencing of breast cancer lung metastasis and adjacent normal tissue
Dataset
EGAD00001015769
-
ESGI-Identification of novel genes and mechanisms leading to Primary Ciliary Dyskinesia
Dataset
EGAD00001001092
-
Multiregion Whole Exome sequencing of pHGG and DIPG
Dataset
EGAD00001004114
-
Role of Epigenetic Memory in Human Induced Pluripotent Stem Cells Pilot
Dataset
EGAD00001000828
-
Bulk RNA-seq dataset of Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Dataset
EGAD00001015508
-
Dichotomous regulation of lysosomes by MYC and TFEB controls hematopoietic stem cell fate
Dataset
EGAD00001006884
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
NICHD Genomic and Proteomic Network for Preterm Birth Research (GPN)
Study
phs000714
-
Type 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008
Study
phs000180
-
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Study
phs002313
-
RNA-Seq of Whole Blood from Patients with Intracranial Aneurysms
Study
phs003072
-
NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI)
Study
phs000279
-
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Study
phs001222
-
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Study
phs000345
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Geographical structure and differential natural selection among North European populations
Study
EGAS00000000033
-
Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
-
Multiomic spatial landscape of innate immune cells at central nervous system borders
Study
EGAS50000000030
-
Analysis of AR Gene Rearrangements in Prostate Cancer
Study
phs001223
-
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Study
phs000893
-
Genetic Effects on Gene Expression and Splicing during Human Neurogenesis
Study
phs002493
-
Nasopharynx Cancer Whole Exome Sequencing
Study
phs001244
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
Reproductive Health in Men and Women with Vasculitis
Study
phs001382
-
Genome-wide Identification of Variants Affecting Early Human Brain Development
Study
phs001122
-
High-Throughput LINE-1 Retrotransposon Discovery in Humans
Study
phs000273
-
NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Study
phs001941
-
Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal
Study
phs003003
-
NHLBI TOPMed: Pediatric Asthma Controller Trial (PACT)
Study
phs001730
-
Interpreting molecular role of DNA variants associated with Crohn's Disease through integrative analysis of open chromatin, epigenome and transcriptome data in diverse and relevant tissues and cells
Study
phs001418
-
Deep Sequencing Studies for Cannabis and Stimulant Dependence
Study
phs001458
-
Single-cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation
Study
phs001276
-
Somatic Mutations and Cell Lineage in the Human Brain
Study
phs001485
-
Rare Mendelian Disease in Old Order Amish and Mennonite Patients
Study
phs000623
-
Gut Microbiome and Types of Colorectal Polyps
Study
phs001381
-
The Genomic Landscape of Interval Colorectal Cancers
Study
phs003093
-
ALLELE Consortium Glioblastoma Project
Study
phs003000
-
Deterministic Evolution and Stringent Selection During Pre-Neoplasia
Study
phs003249
-
Unraveling the Genetic Architecture of Diabetic Retinopathy in South India
Study
phs002116
-
Type I Interferon Exacerbates Mycobacterium Tuberculosis Induced Human Macrophage Death
Study
phs003607
-
Integrative Analysis for Multi-Omics Data in Non-Small-Cell Lung Cancer
Study
phs003113
-
Ipilimumab and Decitabine in Treating Patients With Relapsed or Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia
Study
phs003015
-
Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer
Study
EGAS50000000297
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. WES
Study
EGAS50000000568
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. RNA-Seq
Study
EGAS50000000567
-
IL-17B uses IL-17RA and IL-17RB to induce Type-2 inflammation from human lymphocytes
Study
EGAS50000000579
-
Integrative Molecular Characterization of Breast Cancer
Study
phs002419
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Study
EGAS50000000471
-
MP2PRT: Genomic and Molecular Characterization of Biomarkers Associated with Tumor Angiogenesis, DNA Repair, and Immunologic Tolerance using Samples from the NRG Oncology Phase 3 Randomized Trial, GOG-0240 (NCT00803062)
Study
phs002293