利用下一代测序数据进行全基因组测序分析

Chi Kent Ho, Xiaohui Cui, Sharon Grubner, Christopher A. Larson, Ying Wei, Paul K. Flook
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引用次数: 1

摘要

下一代测序(NGS)技术已经彻底改变了生物科学,对发现基因功能及其与疾病状况的关系变得非常宝贵。NGS技术的快速创新使得以越来越低的成本生产大量序列数据成为可能。然而,不断增加的吞吐量加上这些技术的日益普及,给下游数据分析带来了重大挑战。在这里,我们概述了NGS方法和关键的二次分析管道,重点介绍了Illumina提供的技术。作为一个案例研究,我们强调了在癌症研究中的潜在应用。©2016 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole-Genome Sequencing Analysis Using Next-Generation Sequencing Data

Next-generation sequencing (NGS) technologies have revolutionized the biosciences and become invaluable to the discovery of gene function and its involvement in disease conditions. The fast pace of innovation in NGS technologies has enabled the production of huge volumes of sequence data at progressively lower cost. However, the increasing throughput combined with the growing accessibility of these technologies poses significant challenges for downstream data analysis. Here, we provide an overview of NGS methods and key secondary analysis pipelines with a focus on technology provided by Illumina. As a case study, we highlight potential applications in cancer research. © 2016 by John Wiley & Sons, Inc.

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