-
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis
Study
phs000589
-
Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression
Study
phs000713
-
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Study
phs000486
-
Blood Transcriptome Profiling Following Seizures
Study
phs003460
-
Investigating Delayed-Onset Drug Hypersensitivity Reactions Prospectively
Study
phs003344
-
Sequencing of 3D Organoids Derived From Colorectal Cancer Patients
Study
phs003965
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Study
phs001489
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
Single_cell_measurements_to_characterise_B_cell_repopulation_in_SLE_after_rituximab_therapy__a_pilot_study
Study
EGAS00001006798
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
Genetic Determinants of Viral Clearance in HCV-Infected Populations
Study
phs000248
-
Genomic Analyses in Neoadjuvant Immunotherapy-Treated Head and Neck Cancers
Study
phs002864
-
Chromatin remodeling enhances MAP3K8 expression in HAM: a key pathogenesis for therapeutic intervention
Study
JGAS000835
-
Inherited chromosomally-integrated human herpesvirus 6A/B (HHV-6A/B) genome sequences in the Japanese population
Study
JGAS000240
-
Treg cell subset-specific gene expression patterns in human head and neck cancer
Study
JGAS000135
-
Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Study
EGAS00001002443
-
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Study
EGAS00001003893
-
Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq
Study
EGAS00001002877
-
This study generated Oxford Nanopore long read sequencing data of cancer cell line mixtures for validating long-read variant calls in cancer genomics
Study
EGAS00001008107
-
Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000871
-
Comparison of Custom Capture for Targeted Next Generation DNA Sequencing
Study
phs000811
-
Chromoanasynthesis as a Cause of Jacobsen Syndrome
Study
phs002036
-
A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC
Study
phs001111
-
Genome-Wide Discovery of Novel Colon Cancer Predisposing Mutations
Study
phs000824
-
eMERGE Geisinger eGenomic Medicine (GeM) Abdominal Aortic Aneurysm Project (AAAP)
Study
phs000387
-
Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study
Study
phs000472
-
Single-Cell DNA and RNA Sequencing over A 29-Year Period of A CLL Patient Demonstrating Evolution of Multiple Cell Clones
Study
phs001181
-
The Cardiopulmonary Effects of Particulate Exposure
Study
phs000968
-
CPTAC: Microscaled Proteogenomic Methods for Precision Oncology
Study
phs001907
-
Functionally Active Copy Number Variants Associated with Prostate Cancer Risk
Study
phs000487
-
NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy)
Study
phs000581
-
Epigenome Wide DNA Methylation Study for Osteoporosis Risk
Study
phs001960
-
Epigenetic Landscape of Human Parathyroids
Study
phs003302
-
Circulating, Cell-Free DNA Methylation Patterns Indicate Cellular Sources of Allograft Injury after Liver Transplant
Study
phs003610
-
Whole Genome Sequencing Consortium on Frontotemporal Dementia With Underlying TDP-43 Pathology
Study
phs003309
-
Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer
Study
EGAS50000000923
-
10x Multiome from Human Fetal Heart
Study
phs003778
-
dbGaP Collection: NIH Autism -omics Studies
Study
phs000764
-
Health Information National Trends Survey-SEER (HINTS-SEER)
Study
phs004065
-
Whole genome sequencing data of pediatric B-other subtype acute lymphoblastic leukemia
Study
EGAS50000001497
-
Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Study
EGAS00001003853
-
CD36 defines CML cells less sensitive to imatinib
Study
EGAS00001002421
-
Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
-
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585