Evidence map›Paper›PMID 30967115›Full record

ArticleBMC genomics2019

Signal enrichment with strain-level resolution in metagenomes using topological data analysis.

Aldo Guzmán-Sáenz, Niina Haiminen, Saugata Basu, Laxmi Parida

Abstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Aldo Guzmán-SáenzComputational Biology Center, IBM T. J. Watson Research Center, Yorktown Heights, NY, USA.
Niina HaiminenComputational Biology Center, IBM T. J. Watson Research Center, Yorktown Heights, NY, USA.
Saugata BasuDepartment of Mathematics, Purdue University, West Lafayette, IN, USA.
Laxmi ParidaComputational Biology Center, IBM T. J. Watson Research Center, Yorktown Heights, NY, USA. parida@us.ibm.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA metagenome is a collection of genomes, usually in a micro-environment, and sequencing a metagenomic sample en masse is a powerful means for investigating the community of the constituent microorganisms. One of the challenges is in distinguishing between similar organisms due to rampant multiple possible assignments of sequencing reads, resulting in false positive identifications. We map the problem to a topological data analysis (TDA) framework that extracts information from the geometric structure of data. Here the structure is defined by multi-way relationships between the sequencing reads using a reference database.

resultsBased primarily on the patterns of co-mapping of the reads to multiple organisms in the reference database, we use two models: one a subcomplex of a Barycentric subdivision complex and the other a Čech complex. The Barycentric subcomplex allows a natural mapping of the reads along with their coverage of organisms while the Čech complex takes simply the number of reads into account to map the problem to homology computation. Using simulated genome mixtures we show not just enrichment of signal but also microbe identification with strain-level resolution.

conclusionsIn particular, in the most refractory of cases where alternative algorithms that exploit unique reads (i.e., mapped to unique organisms) fail, we show that the TDA approach continues to show consistent performance. The Čech model that uses less information is equally effective, suggesting that even partial information when augmented with the appropriate structure is quite powerful.

Indexed as

AlgorithmsData AnalysisMetagenomeBacteriaHigh-Throughput Nucleotide SequencingMetagenomicsSequence Analysis, DNAFalse positivesMetagenomicsMulti-mapping readsTopological data analysis

Identifiers

PMID30967115
PMCPMC6456948

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.