2017
DOI: 10.1101/225342
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High-throughput ANI Analysis of 90K Prokaryotic Genomes Reveals Clear Species Boundaries

Abstract: A fundamental question in microbiology is whether there is a continuum of genetic diversity among genomes or clear species boundaries prevail instead. Answering this question requires robust measurement of whole-genome relatedness among thousands of genomes and from diverge phylogenetic lineages. Whole-genome similarity metrics such as Average Nucleotide Identity (ANI) can provide the resolution needed for this task, overcoming several limitations of traditional techniques used for the same purposes. Although … Show more

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Cited by 535 publications
(717 citation statements)
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“…) and digital DNA–DNA hybridisation (dDDH; Fig. S3) comparisons, these isolates are mainly related to three genospecies of R. leguminosarum , gsE (27 strains), gsC (10 strains) and gsB (3 strains), that have been previously identified in European isolates (Kumar et al , ; Jain et al , ; Cavassim et al , ). Eight strains belonged to two other genospecies that were not observed in these previous studies.…”
Section: Resultsmentioning
confidence: 79%
“…) and digital DNA–DNA hybridisation (dDDH; Fig. S3) comparisons, these isolates are mainly related to three genospecies of R. leguminosarum , gsE (27 strains), gsC (10 strains) and gsB (3 strains), that have been previously identified in European isolates (Kumar et al , ; Jain et al , ; Cavassim et al , ). Eight strains belonged to two other genospecies that were not observed in these previous studies.…”
Section: Resultsmentioning
confidence: 79%
“…Contig sequences were aligned to raw data using BWA (Li & Durbin, ) and placed into taxonomic bins with MetaBat2 (Kang, Froula, Egan, & Wang, ) using a minimum contig length of 2,000 bp. The comparison and dereplication of recovered genomes bins were completed using dRep (Olm, Brown, Brooks, & Banfield, ) with minimum primary Average Nucleotide Identity (ANI) 60% (Varghese et al., ) and minimum secondary ANI 95% (Jain, Rodriguez‐R, Phillippy, Konstantinidis, & Aluru, ). CheckM (Parks, Imelfort, Skennerton, Hugenholtz, & Tyson, ) was used to determine completeness and contamination of the best genomes selected by dRep analysis.…”
Section: Methodsmentioning
confidence: 99%
“…The relatedness between the 15 reference genomes recruiting the highest portion of reads (Supporting Information Table S7) was then estimated based on Average Nucleotide Identity (ANI) and Mash genome distances using FastANI (ver. 1.1) (Jain et al ., ) and Mash (ver. 2.1) (Ondov et al ., ) (Supporting Information Fig.…”
Section: Methodsmentioning
confidence: 99%