-
Upper cortical layer-driven network impairment in schizophrenia
Study
EGAS00001006495
-
Human NXPE1 mediates variation in sialic acid O-acetylation in Colon Tissue
Study
EGAS00001007704
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
-
RNA sequencing from patient-derived intestinal organoids
Dataset
EGAD50000000492
-
Exome sequences of AL amyloidosis (ALA), multiple myeloma (MM) and ALA+MM hematological malignancies
Dataset
EGAD00001006047
-
Single cell transcriptomic data of human gut macrophages
Dataset
EGAD00001007765
-
Myeloma Genome Project Targeted Sequencing Panel - Oxford Data
Dataset
EGAD00001008735
-
Disease specific alterations in the olfactory mucosa of patients with Alzheimer’s disease
Dataset
EGAD00001008560
-
Clonal origin of lineage switch leukemia following CAR-T cell and blinatumomab therapy
Dataset
EGAD00001009161
-
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from 4 post-mortem neuropathologically-confirmed control individuals ( anterior prefrontal cortex & cerebellar cortex – 4 individuals, putamen- 3 individuals)
Dataset
EGAD00001009264
-
RNA-seq BAM files from newborn screening dried blood spot samples
Dataset
EGAD00001005009
-
The Natural History of Human Prostate Cancer
Dataset
EGAD00001000689
-
WGBS data (CancerLocator study) of cell-free DNA derived from human blood
Dataset
EGAD00001003168
-
The UCSD / O'Connor "TSP" (Twin/Sibling/Pedigree) Resource in Hypertension
Study
phs002230
-
Security Overview
Documentation
about/security
-
Parkinson's Disease Cognitive Genetics Consortium (PDCGC) Stage I, NeuroX Dataset
Study
phs001664
-
Genome-Wide associations of Lung Health Study (LHS)
Study
phs000335
-
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
-
Virginia PrIMeD Study
Study
phs003609
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
Primary Prostate Tumor Tissue DNA Methylation Profiles
Study
phs001921
-
Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)
Study
phs000361
-
Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Study
phs002632
-
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Study
phs001252
-
Transcriptomic Characterization of Human Innate T Cells
Study
phs002007
-
Whole Genome Sequencing in the Inner City Asthma Consortium (ICAC) Cohorts
Study
phs002921
-
Kids First: Whole Genome Sequencing of Nonsyndromic Craniosynostosis
Study
phs001806
-
NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Study
phs001467
-
Nanobody-Tethered Transposition Allows for Multifactorial Chromatin Profiling at Single-Cell Resolution
Study
phs003068
-
Genetic Epidemiology of Ovarian Cancer Histotypes
Study
phs003140
-
Genomics of Circulating Tumor Cells
Study
phs000717
-
KRT17High/CXCL8+ Tumor Cells Display Both Classical and Basal Features and Regulate Myeloid Infiltration in the Pancreatic Cancer Microenvironment
Study
phs003436
-
Human Blastocyst 10X Single Cell RNA Sequencing
Study
phs003122
-
Systems Analysis of Single-Cell Heterogeneity Underlying Glioma Drug Resistance
Study
phs003501
-
Novel immunodeficiency caused by homozygous mutations of SLC19A1
Study
EGAS50000000356
-
Programs, Origins, and Immunomodulatory Functions of Myeloid Cells in Gliomas
Study
phs003756
-
The taxonomic composition of the human microbiome of CRC patients and healthy donors
Study
EGAS50000000759
-
Transcriptomic hallmarks and RNA isoform diversity in human neurodegenerative disease
Study
EGAS50000000132
-
Immunogenetics of BCG Vaccination and Pediatric Tuberculosis
Study
phs003406
-
Mind Body Study: A Sub-Study on Psychosocial Factors and Microbiomes of Nurses in the Nurse's Health Study II
Study
phs003786
-
Defining Cutaneous Gene Expression Signatures in Juvenile Dermatomyositis
Study
phs003884
-
Omic Studies in Children's Respiratory and Environmental Workgroup (CREW) Cohorts
Study
phs004036
-
Biallelic loss of function PAX4 variants are a Novel Cause of Transient Neonatal Diabetes
Study
EGAS50000000857
-
Whole exome sequencing of bladder tumors
Study
EGAS50000001248
-
Effective screening strategy for deafness using a new-genetation sequencing platform: a consecutive analysis
Study
JGAS000032
-
MATISSE WES and bulk RNA-sequencing data
Study
EGAS50000001003
-
Global Anaplastic Thyroid Cancer Initiative
Study
EGAS00001002234
-
Duplexseq_of_the_interstrand_crosslinks_WGS
Study
EGAS00001006545
-
scRNA-seq of HSPC treated with gemcitabine and carbplatin
Study
EGAS00001004381