Improving metagenomic analysis with novel algorithms and technologies

利用新颖的算法和技术改进宏基因组分析

• 批准号: 10029180
• 负责人: Iman Hajirasouliha
• 金额: $ 42.18万
• 依托单位: WEILL MEDICAL COLL OF CORNELL UNIV
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-01 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10029180
• 关键词: Algorithms; Bar Codes; Benchmarking; Biological Assay; Chromium; Classification; Clinical; Clinical Research; Collaborations; Communities; Complex; Computing Methodologies; DNA Sequence; DNA sequencing; Data Set; Detection; Development; Ensure; Genes; Genomics; Health; Human; Industrialization; Ink; Laboratories; Link; Metagenomics; Methods; Microbe; Molecular; Operative Surgical Procedures; Organism; Pathogenicity; Pathology; Pilot Projects; Reagent; Recovery; Research; Sampling; Shotguns; Special Hospitals; System; Techniques; Technology; Work; clinically relevant; computerized tools; cost; high standard; improved; innovation; large scale data; metagenome; microbiome; microbiome research; nanopore; next generation sequencing; novel; novel strategies; whole genome

SUMMARY/ABSTRACT Microbiome research through sequencing is becoming increasingly important for clinical studies. The human commensal microbiomes have been shown to have a wide variety of potential health impacts. However, our ability to genetically assay microbes is still limited. Microbiomes are extremely complex and standard short-read sequencing technologies often do not provide sufficient basis for the recovery of relevant genes and organisms. Low-input and low-cost linked-read DNA sequencing technologies, such as the 10x Genomics chromium system, have recently emerged with unprecedented promise for de novo assembly of whole genome or metagenome samples. These technologies employ a novel molecular barcoding technique which offers long-range information over standard high-throughput short read, next-generation sequencing, while still at reasonable reagent and low-costs. We plan to develop several innovative novel algorithms to fully leverage barcoded reads in a fast manner to improve several integral and challenging applications, in particular: improving metagenome assembly and leveraging the increased sensitivity to low abundance genomic information in order to identify clinically relevant and potentially pathogenic organisms that can inform clinical decisions. All our proposed methods and computational tools will be made freely available with extensive documentations for the community to use. To ensure the utility of our methods we plan to extensively apply them to a wide range of research and clinical shotgun metagenome data sets, in my laboratory and through various established local, external and industrial collaborations. We also plan to collect control samples and sequence them using multiple platforms (Illumina, 10x Genomics, Loop Genomics Read Cloud, UTS TELL-SEQ, Oxford Nanopore) for benchmarking. We will also use our proposed methods to improve the detection and classification of low abundance organisms in clinical samples. We will launch two pilot projects in collaborations with our Department of Pathology and Hospital for Special Surgery (HSS). Successful completion of this project will provide fast and scalable computational methods that can be applied to large-scale data sets.

摘要/摘要 通过测序进行微生物组研究对于临床研究正变得越来越重要。 人类共生微生物群已被证明具有多种潜在的健康 影响。然而，我们对微生物进行基因检测的能力仍然有限。微生物群是 极其复杂和标准的短读测序技术通常无法提供 为恢复相关基因和生物体提供了充分的基础。 低投入、低成本的连锁阅读DNA测序技术，如10x基因组学 铬系统，最近出现了前所未有的前景，从头组装 全基因组或超基因组样本。这些技术使用了一种新的分子 一种条形码技术，通过标准的高吞吐量短数据提供远距离信息 阅读，下一代测序，同时仍以合理的试剂和低成本进行。我们计划 开发几种创新的新算法，以快速充分利用条形码读取 改进几个完整且具有挑战性的应用程序，特别是：改进元基因组 组装和利用对低丰度基因组信息的增加的敏感性 以确定临床上相关的和潜在的病原体，这些微生物可以为临床提供信息 决定。 我们建议的所有方法和计算工具都将免费提供给广泛的 供社区使用的文档。为了确保我们的方法的实用性，我们计划 将它们广泛应用于广泛的研究和临床猎枪元基因组数据集， 在我的实验室里，并通过各种建立起来的本地、外部和行业合作。 我们还计划收集控制样本并使用多个平台对它们进行测序(Illumina， 10倍基因组学、环路基因组学读云、UTS Tell-SEQ、牛津纳米孔) 标杆管理。我们还将使用我们提出的方法来改进检测和 临床标本中低丰度生物的分类。开展两个试点。 与我们的病理科和特殊外科医院(HSS)合作。 该项目的成功完成将提供快速和可扩展的计算方法， 可应用于大规模数据集。