-
Framingham Heart Study-Cohort (FHS-Cohort) - Imaging
Study
phs003593
-
The Human Virome in Children and its Relationship to Febrile Illness
Study
phs000264
-
Genome-Wide Association Study of Anorexia Nervosa (Price Foundation, Klarman Family Foundation, Center for Applied Genomics at the Children's Hospital of Philadelphia, Scripps Translational Sciences Institute Clinical Translational Science Award)
Study
phs000679
-
Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma)
Study
phs000328
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
Converging and evolving immuno-genomic routes towards immune escape in breast cancer
Dac
EGAC50000000074
-
Thoracic Patient-Derived Xenografts
Study
phs001192
-
TOPARP-B patient cell-free DNA WGS
Study
EGAS50000000280
-
Exome_sequencing_Parkinson_s_disease_patients
Study
EGAS00001000151
-
McGill EMC Release 4 in tissue "skeletal muscle tissue"
Dataset
EGAD00001001288
-
Premalignant SOX2 in ovarian cancer patients
Dataset
EGAD00001002734
-
Exome_NanoSeq__Thyroid_
Study
EGAS00001007175
-
Targeted_NanoSeq___Thyroid
Study
EGAS00001007647
-
BCG-Flu_Challenge_Study_RNAseq_Human_01
Study
EGAS50000001677
-
LLDeep DAG2+ scRNA-seq in PBMCs
Dataset
EGAD00010001315
-
Enhancing OSCC Prediction: The Prognostic Power of WPOI and Tumor Budding, and the Limited Impact of Molecular Resection Margins
Study
EGAS50000000074
-
Genomic Sequencing of Solitary Fibrous Tumors
Study
phs000568
-
Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform
Study
phs002123
-
Washington University Coronary Artery Disease Study
Study
phs001227
-
RareBliss: Rare Bipolar Loci Identification Through Sequencing Study
Study
phs001358
-
Whole Exome Sequencing of Six Signet Ring/Plasmacytoid Variant Bladder Tumors
Study
phs001064
-
DCLRE1B/Apollo germline mutations associated with renal cell carcinoma
Study
EGAS50000000216
-
PDX gene expression
Study
EGAS50000000084
-
scRNA-seq dataset, RCC
Dataset
EGAD50000000566
-
Sex Differences in MAGEL2 Gene Promoter Methylation in High Functioning Autism - Trends from a Pilot Study Using Nanopore Cas9 Targeted Long Read Sequencing
Study
EGAS50000000508