Evidence map›Paper›PMID 33828908›Full record

ArticlePeerJ2021

LINflow: a computational pipeline that combines an alignment-free with an alignment-based method to accelerate generation of similarity matrices for prokaryotic genomes.

Long Tian, Reza Mazloom, Lenwood S Heath, Boris A Vinatzer

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In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

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5citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Meta-analysis of theMicrobial genomics · 2022
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  2. Genomic insights intoMicrobiology spectrum · 2026
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Long Tian *School of Plant and Environmental Sciences, Virginia Tech, Blacksburg, VA, USA.
Reza Mazloom *Department of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Lenwood S HeathDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.ORCID 0000-0003-1608-431X
Boris A VinatzerSchool of Plant and Environmental Sciences, Virginia Tech, Blacksburg, VA, USA.ORCID 0000-0003-4612-225X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComputing genomic similarity between strains is a prerequisite for genome-based prokaryotic classification and identification. Genomic similarity was first computed as Average Nucleotide Identity (ANI) values based on the alignment of genomic fragments. Since this is computationally expensive, faster and computationally cheaper alignment-free methods have been developed to estimate ANI. However, these methods do not reach the level of accuracy of alignment-based methods.

methodsHere we introduce LINflow, a computational pipeline that infers pairwise genomic similarity in a set of genomes. LINflow takes advantage of the speed of the alignment-free sourmash tool to identify the genome in a dataset that is most similar to a query genome and the precision of the alignment-based pyani software to precisely compute ANI between the query genome and the most similar genome identified by sourmash. This is repeated for each new genome that is added to a dataset. The sequentially computed ANI values are stored as Life Identification Numbers (LINs), which are then used to infer all other pairwise ANI values in the set. We tested LINflow on four sets, 484 genomes in total, and compared the needed time and the generated similarity matrices with other tools.

resultsLINflow is up to 150 times faster than pyani and pairwise ANI values generated by LINflow are highly correlated with those computed by pyani. However, because LINflow infers most pairwise ANI values instead of computing them directly, ANI values occasionally depart from the ANI values computed by pyani. In conclusion, LINflow is a fast and memory-efficient pipeline to infer similarity among a large set of prokaryotic genomes. Its ability to quickly add new genome sequences to an already computed similarity matrix makes LINflow particularly useful for projects when new genome sequences need to be regularly added to an existing dataset.

Indexed as

Average nucleotide identityComparative genomicsGenome-based taxonomyGenomic similarityPhylogenomicsProkaryotes

Identifiers

PMID33828908
PMCPMC8000461

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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.