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Exome sequencing in HIV+ Viremic Non-Progressors (VNPs) and HIV+ Progressors
Study
EGAS50000000079
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000158
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000160
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000162
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Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
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A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing
Study
EGAS00001003127
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Improved detection of colibactin-induced mutations by genotoxic E. coli in organoids and colorectal cancer
Study
EGAS50000000212
-
Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer
Study
EGAS50000000297
-
Somatic mutations of non-malignant T cells
Study
EGAS50000000237
-
Human Brain Small Extracellular Vesicles Contain Selectively-Packaged, Full-Length mRNA
Study
EGAS50000000029
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
Single-cell RNA sequencing of human skin tumors (BCC, SCC and Melanoma)
Study
EGAS50000000365
-
FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
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A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart
Study
EGAS00001003996
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Single cell chromatin accessibility allows analysis of the transposable element landscape, revealing shared features of immune tissue-residency
Study
EGAS50000000350
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Study
EGAS50000000471
-
Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes
Study
EGAS50000000536
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. WES
Study
EGAS50000000568
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. RNA-Seq
Study
EGAS50000000567
-
Genome sequencing identifies splice-disrupting variants in childhood heart disease
Study
EGAS50000000586
-
High number of somatic mutations found in the healthy blood compartment of a 115-year-old woman reveals oligoclonal hematopoiesis
Study
EGAS00001000660
-
Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Study
EGAS00001003363
-
Spatial atlas of human atherosclerosis highlights role of the microvasculature in disease
Study
EGAS50000000660
-
Ultra-sensitive ctDNA monitoring required for predicting response and resistance to immunotherapy in advanced melanoma
Study
EGAS50000000550
-
Oncogenic FOXL2C134W has gain-of-function chromatin remodeling activity that reprograms glucocorticoid receptor occupancy to promote ovarian granulosa cell tumor growth
Study
EGAS50000000622
-
MutWP6__CRUK_Grand_Challenge_Mutographs_of_Cancer__alkylating_agents
Study
EGAS00001003637
-
MutWP6__CRUK_Grand_Challenge_Mutographs_of_Cancer__oncology_agents
Study
EGAS00001004125
-
Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
-
IL-17B uses IL-17RA and IL-17RB to induce Type-2 inflammation from human lymphocytes
Study
EGAS50000000579
-
Epstein-Barr Virus status drives morphological and molecular intra-tumour heterogeneity in gastric cancer: insights from a case report and literature review
Study
EGAS50000000706
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
Nivolumab plus chemotherapy or ipilimumab in gastroesophageal cancer: CheckMate 649 biomarker analyses
Study
EGAS50000000747
-
Pyjacker identifies enhancer hijacking events in acute myeloid leukemia including MNX1 activation via deletion 7q
Study
EGAS50000000743
-
Single cell sequencing data of PBMC and CSF from a cohort of Multiple Sclerosis patients and other neurological disease controls
Study
EGAS50000000739
-
SeqControl: Process Control for DNA Sequencing
Study
EGAS00001000899
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia
Study
EGAS00001004808
-
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Study
EGAS00001001002
-
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Study
EGAS00001001018
-
Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
-
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Study
EGAS00001001190
-
Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer
Study
EGAS00001004486
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas
Study
EGAS00001001284
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Study
EGAS00001001310