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SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy

机译:小鼠细胞系的SNP阵列分析可鉴定其起源菌株并揭示交叉污染和广泛的非整倍性

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摘要

BackgroundThe crisis of Misidentified and contaminated cell lines have plagued the biological research community for decades. Some repositories and journals have heeded calls for mandatory authentication of human cell lines, yet misidentification of mouse cell lines has received little publicity despite their importance in sponsored research. Short tandem repeat (STR) profiling is the standard authentication method, but it may fail to distinguish cell lines derived from the same inbred strain of mice. Additionally, STR profiling does not reveal karyotypic changes that occur in some high-passage lines and may have functional consequences. Single nucleotide polymorphism (SNP) profiling has been suggested as a more accurate and versatile alternative to STR profiling; however, a high-throughput method for SNP-based authentication of mouse cell lines has not been described.
机译:背景误识别和污染细胞系的危机困扰着生物研究界数十年。一些存储库和期刊已经听取了对人类细胞系进行强制认证的呼吁,尽管对小鼠细胞系的错误识别在赞助研究中很重要,但很少受到关注。短串联重复序列(STR)分析是标准的验证方法,但可能无法区分源自同一近交系小鼠的细胞系。此外,STR分析不能揭示某些高通量谱系中发生的核型变化,并且可能具有功能性后果。有人提出单核苷酸多态性(SNP)分析是STR分析的一种更准确和通用的替代方法。但是,尚未描述用于基于SNP的小鼠细胞系验证的高通量方法。

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