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MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
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Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Study
EGAS00001004019
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Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002607
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Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Study
EGAS00001002626
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Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
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We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670
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The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
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Alternative splicing isoforms in patient-derived hepatocellular carcinoma cells
Study
EGAS00001002697
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Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens
Study
EGAS00001005786
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Brain_Disease_Wellcome_Leap_Delta_Tissue_DNA
Study
EGAS00001005799