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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
-
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
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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
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
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A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Study
EGAS00001002272
-
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples
Study
EGAS00001002631
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Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678