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Risk-Stratified Therapy for Acute Myeloid Leukemia in Down Syndrome
Study
phs004081
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Measles oncolytic virus as an immunotherapy for recurrent/refractory pediatric medulloblastoma and atypical teratoid rhabdoid tumor
Study
EGAS50000000811
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Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
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Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
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Searching for variants associated with endometriosis
Study
EGAS00001001741
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Single cell RNA sequencing and Whole Genome Sequencing on different cells from the same sample for a triple negative patient derived xenograft and ovarian cancer cell lines.
Study
EGAS00001003387
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We describe a method to culture organoids from adult human kidney tissue and describe applications for the culture system.
Study
EGAS00001002729
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RNA-seq profiling of NKX6.1 reporter iPSC lines for isolation and analysis of functionally relevant neuronal and pancreas populations
Study
EGAS00001002802
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Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
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Adult human kidney organoids originate from CD24+ cells and represent an advanced model for adult polycystic kidney disease
Study
EGAS00001006551
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A clinically applicable connectivity signature for glioblastoma includes the tumor network driver CHI3L1
Study
EGAS00001007611
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Distribution of ctDNA levels in plasma of early-stage non-small cell lung cancer patients measured using personalised ctDNA analysis
Dataset
EGAD00001006230
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WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001009049
-
WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001010135
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Whole genome analyses of the childhood cancer neuroblastoma
Dataset
EGAD00001000282
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Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: SAFER-COVID - Integration of Testing and Digital Health
Study
phs002540
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Enrichment of PTPRT and JAK2 mutations in lung cancer from African Americans and evidence for increased GI and HRD in LUSC
Study
phs001895
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A National Translational Science Network of Precision-Based Immunotherapy for Primary Liver Cancer (PLC)
Study
phs003074
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Center for Common Disease Genomics (CCDG)-Cardiovascular: University of Pennsylvania Cohort
Study
phs001502
-
EOSC4Cancer Longitudinal Synthetic Colorectal Cancer Genomic data developed at BSC
Dataset
EGAD50000000276
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TIRE-seq: an Integrated Sample Extraction and Transcriptomics Workflow for High Throughput Perturbation Studies
Study
EGAS50000000867
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NGS sequencing data of archival FFPE tumor tissue
Dataset
EGAD50000001371
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Allogeneic induced pluripotent stem (iPS) cell-derived cartilage transplantation for articular cartilage damage in knee joints: a phase I, first-in-human study
Study
EGAS50000001167
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Generation of hypoimmunogenic induced pluripotent stem cells by CRISPR-Cas9 system and detailed evaluation for clinical application
Study
EGAS50000001194
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Integrated Methylation and Copy Number Analysis for Non-invasive Bladder Cancer Detection in Urine
Study
EGAS50000001350
-
ATAC-seq iPSC cells or smNPC cells for allelic imbalance
Study
EGAS50000001579
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Personalized analysis of ctDNA for detection of molecular residual disease and recurrence in a cohort of surgically treated patients with head and neck squamous cell carcinoma
Study
EGAS50000001018
-
Tools
Documentation
tools
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Fixative optimisation study for BRITROC project
Study
EGAS00001001433
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
A Comparative Analysis of Algorithms for Somatic SNV Detection in Cancer
Study
EGAS00001000927
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Whole-genome sequences of single-cell derived clonal samples and bulk blood samples from human
Dataset
EGAD00001007032
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Bulk-tissue paired-end RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Dataset
EGAD00001007698
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Postmortem Single Nuclei and Bulk RNA-seq data of the Motor Cortex and Spinal Cord for Healthy, C9ALS and sALS Patients
Dataset
EGAD00001009686
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PELICAN33 Phenomic Dataset
Dataset
EGAD00001007800
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Platelets contain a repertoire of DNA fragments that map over the human nuclear genome, including tumour-derived DNA in patients with active malignancy.
Dataset
EGAD00001009856
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RNA sequencing of end-stage kidney disease patients with COVID-19
Dataset
EGAD00001009752
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Rare Disease Synthetic Dataset
Dataset
EGAD00001008392
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Dataset
EGAD00001001691
-
RNA-seq profiling of NKX6.1 reporter iPSC lines for isolation and analysis of functionally relevant neuronal and pancreas populations
Dataset
EGAD00001003911
-
Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
-
Investigation of mutational signatures associated with DNMT3A deficiency (2019-04-03)
Dataset
EGAD00001004889
-
Functional genomics approaches to understand osteoarthritis (2019-08-01)
Dataset
EGAD00001005215
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Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease
Study
EGAS00001005342
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Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia
Study
EGAS00001003627
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Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA
Study
EGAS00001003849
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DAC - Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Dac
EGAC00001002549
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Data Access Committee for data from EGAS00001002864: Genome analysis of oesophageal cancer and Barretts oesophagus
Dac
EGAC00001000863
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This DAC is to control access to data contained within dataset EGAS00001001147, for Myeloma XI clinical trial patients.
Dac
EGAC00001000307
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Centre for Genomic Regulation - Beta Cell Genome Regulation Lab
Dac
EGAC00001000853