4.7 Article

On the complexity of haplotyping a microbial community

期刊

BIOINFORMATICS
卷 37, 期 10, 页码 1360-1366

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btaa977

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资金

  1. Aberystwyth University Doctoral Career Development Scholarship
  2. IBERS Doctoral Programme
  3. Coleg Cymraeg Cenedlaethol Academic Staffing Scheme
  4. BBSRC Institute Strategic Programme Grant, Rumen Systems Biology [BB/E/W/10964A01]
  5. DAFM Ireland/DAERA Northern Ireland under the Meth-Abate project [R3192GFS]
  6. EC [818368]
  7. Erasmus+ Programme

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This study discusses the challenges of recovering genomic sequences from microbial communities, introducing the metagenomic individual haplotyping problem and providing software implementations for it. By extending the single individual haplotype problem to microbial communities, the authors have made progress in understanding the evolution and ecology of microbial ecosystems.
Motivation: Population-level genetic variation enables competitiveness and niche specialization in microbial communities. Despite the difficulty in culturing many microbes from an environment, we can still study these communities by isolating and sequencing DNA directly from an environment (metagenomics). Recovering the genomic sequences of all isoforms of a given gene across all organisms in a metagenomic sample would aid evolutionary and ecological insights into microbial ecosystems with potential benefits for medicine and biotechnology. A significant obstacle to this goal arises from the lack of a computationally tractable solution that can recover these sequences from sequenced read fragments. This poses a problem analogous to reconstructing the two sequences that make up the genome of a diploid organism (i.e. haplotypes) but for an unknown number of individuals and haplotypes. Results: The problem of single individual haplotyping was first formalized by Lancia et al. in 2001. Now, nearly two decades later, we discuss the complexity of 'haplotyping' metagenomic samples, with a new formalization of Lancia et al.'s data structure that allows us to effectively extend the single individual haplotype problem to microbial communities. This work describes and formalizes the problem of recovering genes (and other genomic subsequences) from all individuals within a complex community sample, which we term the metagenomic individual haplotyping problem. We also provide software implementations for a pairwise single nucleotide variant (SNV) co-occurrence matrix and greedy graph traversal algorithm.

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