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During the last 10 years, considerable progress has been made in cancer genetics and many cancer diagnoses now rely on molecular biology. Chromosomal abnormalities have been first studied by karyotype analysis then fluorescence in situ hybridisation (FISH), and now new techniques are available, like comparative genomic hybridisation and single nucleotide polymorphism (SNP) arrays, that are becoming more and more affordable in molecular pathology labs. New technologies for genome-wide DNA sequencing are now revealing specific and unbiased information on cancer initiation …
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Provenance and peer review Commissioned; internally peer reviewed.
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