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泛基因组分析十年

Ten years of pan-genome analyses.

机构信息

Novartis (Hellas) S.A.C.I., 12th Km Athens-Lamia North Road, 14451 Metamorfossi, Athens, Greece.

Novartis Vaccines Research, Via Fiorentina 1, 53100 Siena, Italy.

出版信息

Curr Opin Microbiol. 2015 Feb;23:148-54. doi: 10.1016/j.mib.2014.11.016. Epub 2014 Dec 5.

Abstract

Next generation sequencing technologies have engendered a genome sequence data deluge in public databases. Genome analyses have transitioned from single or few genomes to hundreds to thousands of genomes. Pan-genome analyses provide a framework for estimating the genomic diversity of the dataset at hand and predicting the number of additional whole genomes sequences that would be necessary to fully characterize that diversity. We review recent implementations of the pan-genome approach, its impact and limits, and we propose possible extensions, including analyses at the whole genome multiple sequence alignment level.

摘要

下一代测序技术在公共数据库中产生了大量的基因组序列数据。基因组分析已经从单个或少数基因组转变为数百个到数千个基因组。泛基因组分析为估计手头数据集的基因组多样性并预测完全描述该多样性所需的额外全基因组序列数量提供了框架。我们回顾了泛基因组方法的最新实现、它的影响和局限性,并提出了可能的扩展,包括在全基因组多重序列比对水平上的分析。

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