TT-Mars: structural variants assessment based on haplotype-resolved assemblies.

TT-Mars: structural variants assessment based on haplotype-resolved assemblies.
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DOI:
10.1186/s13059-022-02666-2
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发表时间:
2022-05-06
期刊:
影响因子:
12.3
通讯作者:
--
中科院分区:
生物学1区
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变体基准测试通常通过将测试调用集与变体的金标准集进行比较来执行。在基因组的重复区域中,可能难以确定调用的真实性,例如,当不同的比对评分度量在相同数据上提供同等支持但不同的变体调用时。在这里,我们提供了一种替代方法,TT-Mars,它利用了最近生产的高质量的单倍型解析基因组组件,通过提供错误的发现率,基于他们的呼叫如何反映组件的内容,而不是比较呼叫本身。在线版本包含补充材料,可在(10.1186/s13059-022-02666-2)获得。
Variant benchmarking is often performed by comparing a test callset to a gold standard set of variants. In repetitive regions of the genome, it may be difficult to establish what is the truth for a call, for example, when different alignment scoring metrics provide equally supported but different variant calls on the same data. Here, we provide an alternative approach, TT-Mars, that takes advantage of the recent production of high-quality haplotype-resolved genome assemblies by providing false discovery rates for variant calls based on how well their call reflects the content of the assembly, rather than comparing calls themselves. The online version contains supplementary material available at (10.1186/s13059-022-02666-2).
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