Department of Microbiology, Oregon State University, Corvallis, OR 97331, United States.
Curr Opin Microbiol. 2012 Oct;15(5):605-12. doi: 10.1016/j.mib.2012.07.001. Epub 2012 Jul 23.
Since nucleic acids were first extracted directly from the environment and sequenced, metagenomics has grown to one of the most data-rich and pervasive techniques for understanding the taxonomic and functional diversity of microbial communities. In the last decade, cheaper sequencing has democratized the application of metagenomics and generated billions of reads, revealing staggering microbial diversity and functional complexity. However, cheaper sequencing has come at the cost of reduced sequence length, resulting in poor gene annotation and overestimates of bacterial richness and abundance. Recent improvements in sequencing technology are beginning to provide reads of sufficient length for accurate annotation and assembly of whole operons and beyond, that will once again enable experimental testing of gene function and re-capture the early successes of metagenomic investigations.
自从直接从环境中提取并测序核酸以来,宏基因组学已发展成为最具数据丰富性和普及性的技术之一,用于了解微生物群落的分类和功能多样性。在过去的十年中,更便宜的测序技术使宏基因组学的应用民主化,并产生了数十亿个读数,揭示了惊人的微生物多样性和功能复杂性。然而,更便宜的测序是以降低序列长度为代价的,这导致基因注释不佳,并且细菌丰富度和丰度的估计过高。最近测序技术的改进开始提供足够长度的读取,以便对整个操纵子及其以外的基因进行准确注释和组装,这将再次使基因功能的实验测试成为可能,并重新获得宏基因组研究的早期成功。