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Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
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T-cell receptor sequencing of tumor-infiltrating lymphocytes (TIL) in breast cancer
Study
EGAS00001007125
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IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
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A transcriptomic approach to understand patient susceptibility to pneumonia after abdominal surgery
Study
EGAS00001007229
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cfDNA dataset from the urine supernatant of ovarian cancer patients and healthy controls
Study
EGAS00001007238
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Multi-omic analysis of the tumor microenvironment shows clinical correlations in Ph1 study of atezolizumab +/- SoC in MM
Study
EGAS00001007286
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Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
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Evaluation of somatic mutations in urine samples as a non-invasive method for the detection and molecular classification of endometrial cancer
Study
EGAS00001007396
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Regenerative effects of MSC treatment on busulfan-induced small intestine damaged organoids.
Study
EGAS00001007432
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Ultra-fast deep-learned pediatric CNS tumor classification.
Study
EGAS00001007475
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RNASeq Neoantigen Immunogenicity Landscape
Study
EGAS00001007509
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MethylationEPIC BeadChip samples of pre- and post-5ZA-treated head and neck cancer patients refractory to anto-PD-1 therapy
Study
EGAS00001007998
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Multi-Layered Molecular Profiling Informs the Diagnosis and Targeted Therapy of Desmoplastic Small Round Cell Tumor
Study
EGAS00001007934
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Transcriptomics-driven classification of ALAL
Study
EGAS00001007967
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Dynamics of circulating tumor DNA in acute myeloid leukemia (AML) patients who undergo allogeneic transplantation
Study
EGAS00001007969
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Whole genome sequencing of tumor samples from advanced pre-treated NSCLC patients recruited in a phase I/II single-arm trial utilising CVA21, an oncolytic coxsackie virus, in combination with pembrolizumab.
Study
EGAS00001008258
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European BestAgeing Study on microRNA candidates for cardiovascular disease
Study
EGAS00001008346
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Multi-omic analysis of Down Syndrome in thyroid
Study
EGAS00001007677
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A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Study
EGAS00001006547
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Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers
Study
EGAS00001007242
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H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa
Study
EGAS00001007250
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Tubulointerstitial fibrosis is the histological hallmark of chronic kidney disease (CKD). Hypoxia and inflammation (i.e., interleukin (IL)-1β signalling) are independent mediators of tubulointerstitial fibrosis. However, the physiological response of human kidney tubular cells to IL-1β/IL-1RI signalling under the hypoxic conditions of CKD is poorly understood and remains a clinical imperative for therapeutic targeting. This study reports that hypoxia and IL-1β act in synergy to trigger cell cycle arrest/cellular senescence of ex vivo patient-derived primary proximal tubular epithelial cells (PTECs).
Study
EGAS00001007904
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Identification of intronic sequences promoting natural skipping of ABCA4 exon 15 using long-read transcriptomics and midigene assays
Study
EGAS50000000071
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Blueprint Data Access Committee.
Dac
EGAC00001000135
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Integrating molecular imaging and transcriptomic profiling in advanced HER2-positive breast cancer receiving trastuzumab emtansine (T-DM1): an analysis of the ZEPHIR clinical trial
Study
EGAS50000000470
-
Genomic Profiling of Pediatric Tumors by Cell Free DNA Sequencing
Study
EGAS50000000072
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Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
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A prospective study identifies MisMatch Repair genes as candidate predisposing genes for uveal melanoma.
Study
EGAS50000000914
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Emirati Genome Project subset of 43,608 WGS samples for population-scale variant discovery and allele frequency mapping.
Study
EGAS50000001071
-
Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
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CDK4/6 inhibition in advanced chordoma: final results of the NCT PMO-1601
Study
EGAS00001007985
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mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
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Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
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First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
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Copy number profiling of primary samples and cell lines of retinoblastoma
Study
EGAS00001001715
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In this study, blood-brain barrier (BBB)-forming brain endothelial-like cells were generated from apolipoprotein E gene allele E4 (APOE4, high AD risk) and allele E3 (APOE3, lower AD risk) carrying patient-derived induced pluripotent stem cells (iPSCs). Cells were subsequently exposed to focused ultrasound and microbubbles (FUS+MB) to induce BBB opening and their transcriptome analysed. RNA sequencing (RNA-seq) results demonstrated minimal changes in the gene expression following FUS+MB suggesting safety of FUS+MB application in the clinical setting.
Study
EGAS00001005944
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Local In Time Statistics for processual research
Study
EGAS00001002520
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Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
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RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
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McGill Epigenomics Mapping Centre
Study
EGAS00001000995
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Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
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Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Polymorphisms in the mitochondrial genome are associated with bullous pemphigoid in Germans
Study
EGAS00001003932
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
-
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418