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Multi-institutional collaboration to characterize 5hmC in prostate cancer, both tumor biopsies and cfDNA.
Study
EGAS00001004942
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Dataset
EGAD50000000679
-
Scalable Whole-Exome Sequencing of Cell-Free DNA Reveals High Concordance with Metastatic Tumors
Study
phs001417
-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
-
T cell receptor repertoire in cell-free DNA as a proxy for tumor infiltrates in patients treated with pembrolizumab
Study
EGAS50000001306
-
Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring
Study
EGAS00001004406
-
Methylome sequencing of cell-free DNA and RRBS of solid tissue
Study
EGAS00001006020
-
The effect of pre-analytical and physiological variables on cell-free DNA fragmentation
Study
EGAS00001005748
-
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Study
phs001359
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001238
-
NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001345
-
The Human Phenotype Project (HPP) is a large-scale deep-phenotype prospective longitudinal and ethnically diverse cohort
Study
EGAS00001008040
-
prostate cancer plasma cfRNA
Dataset
EGAD50000001805
-
Copy number profiling of tissue and plasma samples from high grade serous epithelial ovarian cancer patients
Dataset
EGAD00001006422
-
Single Cell Transcriptomics of peripheral immune cells pre- and post-Immune Checkpoint Blockade
Dataset
EGAD00001007942
-
cfDNA methylation profiling in Metastatic Cancer and Cancer of Unknown Primary
Dataset
EGAD00001011178
-
Children's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study
Study
phs000199
-
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
Study
EGAS00001002622
-
mFAST-SeqS
Study
EGAS00001001133
-
Platinum Genomes
Study
phs001224
-
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Study
phs002033
-
Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors
Study
EGAS00001004878
-
Single_Cell_Sequencing_of_Sperm__scSperm_
Study
EGAS00001000935
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
A mathematical model of cell-free DNA fragment size reveals cancer-specific fragmentomic patterns
Study
EGAS50000001560
-
Paired FastQ files from deep targeted DNA sequencing
Dataset
EGAD50000001267
-
IMpower133 (GO30081) clinical data and biomarker data
Dataset
EGAD50000000195
-
DNA methylation-based classification of sinonasal tumors [Proteomics data]
Dataset
EGAD00010002381
-
Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's or Parkinson's disease correlate with disease status and features of pathology
Study
phs000727
-
A prospective multicenter study of plasma ctDNA versus archival tumor tissue to guide FGFR-targeted therapy in metastatic urothelial cancer - Targeted
Study
EGAS50000001450
-
ERBB2/HER2 alterations in ctDNA and metachronous tissues of patients with metastatic urothelial cancer - WGS
Study
EGAS50000001082
-
ERBB2/HER2 alterations in ctDNA and metachronous tissues of patients with metastatic urothelial cancer - Targeted
Study
EGAS50000001081
-
Whole genome sequencing data of paediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001079
-
Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer
Study
EGAS50000000793
-
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
-
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Study
EGAS00001006913
-
RNA sequencing data of pediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001799
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Dataset
EGAD00001006888
-
Aligned Low pass whole genbome sequencing of cell free and tumour DNA from 5 patients with high grade serous ovarian cancer. Samples have been aligned to hg19 and bam files uploaded
Dataset
EGAD50000001632
-
Effects of Metformin on Transcriptomic and Metabolomic Profiles in Breast Cancer Survivors Enrolled in the Randomized Placebo-Controlled MetBreCS Trial
Dataset
EGAD50000001274
-
Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models: validation cohort
Study
EGAS00001006582
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
Tumor Fraction Guided Cell-Free DNA Profiling in Metastatic Cancer Patients
Study
phs002290
-
Circulating, Cell-Free DNA Methylation Patterns Indicate Cellular Sources of Allograft Injury after Liver Transplant
Study
phs003610
-
Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer
Study
EGAS50000000923
-
Copy number variations and fragmentation features in cell-free DNA predict response in advanced non-small cell lung cancer patients under anti-PD-(L)1 therapy
Study
EGAS50000000441
-
Cancer cell and tumor microenvironment biomarkers associated with disease-free survival with adjuvant nivolumab in the phase 3 CheckMate 274 trial
Study
EGAS50000000560
-
All you need to know about our new DAC Portal v2
Blog
new-dac-portal-v2
-
WGS data of paediatric hyperdiploid B cell acute lymphoblastic leukemia (set2)
Dataset
EGAD50000002426