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Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
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Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Study
EGAS00001001018
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GEL_WGS_Comparison
Study
EGAS00001000649
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Genomic study of an AT-AML
Study
EGAS00001004392
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GIST_SSGXVIII_trial_targeted_gene_sequencing
Study
EGAS00001001054
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genome-wide cfDNA methylation analysis
Study
EGAS00001003958
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Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
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Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Study
EGAS00001001084
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Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci
Study
EGAS00001001085
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Sequencing of cell-free DNA from breast cancer patients
Study
EGAS00001004960