-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Vitamin-D-Kids Asthma
Study
phs004051
-
Long-read single-cell RNA sequencing uncovers cell-type specific transcript regulation in COVID-19
Study
EGAS50000001290
-
Multi-modal spatial characterization of tumor-immune microenvironments in diffuse large B-cell lymphoma
Study
EGAS50000001146
-
Ewing's Sarcoma RNA-Seq
Dataset
EGAD00001004188
-
Nasal MicroRNA during Bronchiolitis and Age 6y Asthma: MARC-35 Cohort
Study
phs003564
-
Single Chromatin Fiber Profiling in the Human Brain
Study
phs003771
-
Quantitative analysis of a novel DNA hypermethylation panel using bronchial specimen for lung cancer diagnosis
Dataset
EGAD00010002465
-
RNAseq of 76 samples from Uveal Melanoma tumors
Dataset
EGAD00001004398
-
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
-
NIH RECOVER: A Multi-Site Observational Study of Post-Acute Sequelae of SARS-CoV-2 Infection in Adults
Study
phs003463
-
Neoantigen Immunogenicity Landscapes and Evolution of Tumor Ecosystems During Immunotherapy with Nivolumab
Dataset
EGAD00001011302
-
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): A Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study
Study
phs003066
-
Epidemiologic Architecture for Genes Linked to Environment (EAGLE) MetaboChip Study
Study
phs002767
-
Germline Whole-Exome Sequencing of Lung Cancer in EAGLE
Study
phs002496
-
Cergentis FFPE-TLC
Study
EGAS50000000427
-
NIH RECOVER-Pediatric: Understanding the Long-Term Impact of COVID on Children and Families
Study
phs003461
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
10x genomics single cell RNA-seq and ATAC-seq from 10 pre-menopausal patients fimbriae and ampullary part of the fallopian tube
Study
EGAS50000000628
-
3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
Study
JGAS000159
-
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Study
phs000245
-
Center for Common Disease Genomics [CCDG] - Cardiovascular ATVB: Atherosclerosis Thrombosis and Vascular Biology
Study
phs001592
-
Somatic L1 Retrotransposition in Colorectal Tumors
Study
phs000536
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program - Neuroblastoma
Study
phs003163