Computational challenges in microbiome research

Mihai Pop
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Abstract

Millions of bacteria make our bodies their home. They help keep us healthy, and disruptions in the normal microbiota are believed to contribute to a number of diseases. Cost-effective sequencing technologies have made it possible to sequence the genomes of human-associated microbial communities, leading to the birth of a new scientific discipline - metagenomics. Analyzing the resulting data, however, poses significant computational challenges, in part due to the sheer size of the data-sets, and in part due to the fact that most of the existing computational framework has been established for single organisms. In my talk I will outline several analytical challenges posed by metagenomic applications, and will describe recent results from my lab in the development of tools for analyzing metagenomic data. In particular I will discuss insights from our analysis of diarrheal disease in developing countries, as well as the effective use of co-abundance approaches for linking together data from two large metagenomic studies.
微生物组研究中的计算挑战
数以百万计的细菌以我们的身体为家。它们有助于保持我们的健康,而正常微生物群的破坏被认为是导致许多疾病的原因。具有成本效益的测序技术使得对人类相关微生物群落的基因组进行测序成为可能,从而催生了一门新的科学学科——宏基因组学。然而,分析结果数据带来了重大的计算挑战,部分原因是数据集的绝对规模,部分原因是大多数现有的计算框架都是为单个生物体建立的。在我的演讲中,我将概述宏基因组应用带来的几个分析挑战,并将描述我的实验室在开发分析宏基因组数据的工具方面的最新成果。特别是,我将讨论我们对发展中国家腹泻病分析的见解,以及有效使用共同丰度方法将两个大型宏基因组研究的数据联系在一起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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