Copy Number Variation Pattern for Discriminating MACROD2 States of Colorectal Cancer Subtypes

Copy number variation (CNV) is a common structural variation pattern of DNA, and it features a higher mutation rate than single-nucleotide polymorphisms (SNPs) and affects a larger fragment of genomes. CNV is related with the genesis of complex diseases and can thus be used as a strategy to identify...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Bioeng Biotechnol
Päätekijät: Zhang, ShiQi, Pan, XiaoYong, Zeng, Tao, Guo, Wei, Gan, Zijun, Zhang, Yu-Hang, Chen, Lei, Zhang, YunHua, Huang, Tao, Cai, Yu-Dong
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2019
Aiheet:
Bioengineering and Biotechnology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6930883/
https://ncbi.nlm.nih.gov/pubmed/31921812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fbioe.2019.00407
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