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一种从低覆盖度鸟枪法测序数据中进行阳性遗传鉴定和亲缘关系检测的计算方法。

A computational approach for positive genetic identification and relatedness detection from low-coverage shotgun sequencing data.

机构信息

Department of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.

Department of Ecology and Evolutionary Biology, University of California, Santa Cruz, Santa Cruz, CA, United States.

出版信息

J Hered. 2023 Aug 23;114(5):504-512. doi: 10.1093/jhered/esad041.

Abstract

Several methods exist for detecting genetic relatedness or identity by comparing DNA information. These methods generally require genotype calls, either single-nucleotide polymorphisms or short tandem repeats, at the sites used for comparison. For some DNA samples, like those obtained from bone fragments or single rootless hairs, there is often not enough DNA present to generate genotype calls that are accurate and complete enough for these comparisons. Here, we describe IBDGem, a fast and robust computational procedure for detecting genomic regions of identity-by-descent by comparing low-coverage shotgun sequence data against genotype calls from a known query individual. At less than 1× genome coverage, IBDGem reliably detects segments of relatedness and can make high-confidence identity detections with as little as 0.01× genome coverage.

摘要

有几种方法可以通过比较 DNA 信息来检测遗传相关性或同一性。这些方法通常需要在用于比较的位点上进行基因型调用,无论是单核苷酸多态性还是短串联重复。对于一些 DNA 样本,例如从骨碎片或无根毛发中获得的样本,通常不存在足够的 DNA 来生成足够准确和完整的基因型调用,以进行这些比较。在这里,我们描述了 IBDGem,这是一种快速而强大的计算程序,用于通过将低覆盖率鸟枪法序列数据与已知查询个体的基因型调用进行比较,来检测同系相关的基因组区域。在不到 1×基因组覆盖的情况下,IBDGem 可靠地检测到相关关系的片段,并且可以在低至 0.01×基因组覆盖的情况下进行高置信度的同一性检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50b7/10445519/eb42728c5048/esad041_fig1.jpg

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