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UK10K COHORT TWINSUK
Study
EGAS00001000108
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UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
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UK10K NEURO ASD BIONED
Study
EGAS00001000111
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Whole genome study of Hurthle cell thyroid carcinoma
Study
EGAS00001000940
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Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01
Study
EGAS00001000249
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Illumina HumanCoreExome genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Study
EGAS00001001001
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Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia
Study
EGAS00001001146
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The clonal and mutational evolution spectrum of primary triple negative breast cancers
Study
EGAS00001000132
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33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
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Combining transcription factor binding affinities with open chromatin data for accurate gene expression prediction
Study
EGAS00001002073
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Transcriptomic profiles of chronic lymphocytic leukemia before and after frontline therapy: 5-year results from the randomized CLL14 study
Study
EGAS00001006596
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T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
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Assessing mitochondrial bioenergetics in coronary artery disease: A translational left ventricular tissue study in humans (The AMBITION study).
Study
EGAS00001007351
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Whole exome sequencing data for paired non-serous endometrial and ovarian carcinomas from 27 patients with concurrent tumours.
Study
EGAS00001008259
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Molecular Attributes Underlying Central Nervous System and Systemic Relapse in Diffuse Large B-cell Lymphoma
Study
EGAS00001004057
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Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
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Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
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Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
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Platelet RNAseq data for SLFN14 K219N patients
Study
EGAS00001006339
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Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
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Spatio-temporal Profiling of a Rhabdoid Tumor Case Study
Study
EGAS00001008174
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Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
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Targeted sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas
Study
EGAS00001005680
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The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
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ICU_transcriptomics__Assessing_the_role_of_the_host_immune_response_in_patients_with_ventilator_associated_pneumonia
Study
EGAS00001003074
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Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
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Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
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Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Study
EGAS00001003452
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Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Study
EGAS00001003661
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Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
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Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Study
EGAS00001004145
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Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
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H3.3G34R/V-transformed interneuron progenitors co-opt PDGFRA for gliomagenesis
Study
EGAS00001004301