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AluScanCNV2: An R package for copy number variation calling and cancer risk prediction with next-generation sequencing data.
Hu T, Chen S, Ullah A, Xue H.
Genes Dis. 2018 Sep 8;6(1):43-46. doi: 10.1016/j.gendis.2018.09.001. eCollection 2019 Mar.
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