Identification of genetic variants using bar-coded multiplexed sequencing.

Identification of genetic variants using bar-coded multiplexed sequencing.
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DOI:
10.1038/nmeth.1251
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发表时间:
2008-10
期刊:
影响因子:
48
通讯作者:
Huentelman, Matthew J.
Huentelman, Matthew J.
中科院分区:
生物学1区
文献类型:
--
作者:
Craig, David W.;Pearson, John V.;Szelinger, Szabolcs;Sekar, Aswin;Redman, Margot;Corneveaux, Jason J.;Pawlowski, Traci L.;Laub, Trisha;Nunn, Gary;Stephan, Dietrich A.;Homer, Nils;Huentelman, Matthew J.

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我们开发了一种通用框架,用于在Illumina基因组分析仪上使用在测序之前连接到片段化DNA的简并索引DNA序列条形码对人类基因组的靶向区域进行多重重测序。使用这种方法,多个HapMap个体的DNA在几个ENCODE(DNA元件的ENCyclopedia)区域同时测序。然后,我们评估了使用贝叶斯因子从比对的测序读数中发现多态性并进行基因分型。如果我们要求预测的多态性是先前通过dbSNP鉴定的,或者在重新检查存档的ENCODE迹线时是视觉上明显的,我们观察到使用严格阈值(Ks> 1,000)预测变体的假阳性率为11.3%,使用宽松阈值(Ks>10)的假阳性率为69.6%。相反,假阴性率范围为10.8%至90.8%,其中更严格的临界值发生在较低的覆盖率(< 10个对齐读数)。这些结果表明,>90%的遗传变体是使用多重测序可检测的,只要在多态性碱基处提供足够的覆盖。
We developed a generalized framework for multiplexed resequencing of targeted regions of the human genome on the Illumina Genome Analyzer using degenerate indexed DNA sequence barcodes ligated to fragmented DNA prior to sequencing. Using this method, the DNA of multiple HapMap individuals was simultaneously sequenced at several ENCODE (ENCyclopedia of DNA Elements) regions. We then evaluated the use of Bayes factors for discovering and genotyping polymorphisms from aligned sequenced reads. If we required that predicted polymorphisms be either previously identified by dbSNP or be visually evident upon reinspection of archived ENCODE traces, we observed a false-positive rate of 11.3% using strict thresholds (Ks>1,000) for predicting variants and 69.6% for lax thresholds (Ks>10). Conversely, false-negative rates ranged from 10.8% to 90.8%, with those at stricter cut-offs occurring at lower coverage (< 10 aligned reads). These results suggest that >90% of genetic variants are discoverable using multiplexed sequencing provided sufficient coverage at the polymorphic base.
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