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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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Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
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The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
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TRACERx Renal 100
Study
EGAS00001002793
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Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors
Study
EGAS00001005106
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MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
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Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
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Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Study
EGAS00001005196
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Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Study
EGAS00001003791
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Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228