Barely Significant
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A comprehensive survey of the mutagenic impact of common cancer cytotoxics.

Genome Biol · 2016 · PMC4862131 · PMID 27161042

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highly significantp <0.001actually significant
The most likely explanation for the highly significant reduction of SNV numbers at genes versus intergenic regions ( p <0.001 in case of both cisplatin and cyclophosphamide, χ 2 test) is the activity of transcription-coupled repair (TCR), which can remove single strand lesions in an error-free manner [ 40 ].

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