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Evaluation of taxonomic classification and profiling methods for long-read shotgun metagenomic sequencing datasets.

Authors :
Portik, Daniel M
Portik, Daniel M
Brown, C Titus
Pierce-Ward, N Tessa
Portik, Daniel M
Portik, Daniel M
Brown, C Titus
Pierce-Ward, N Tessa
Source :
BMC bioinformatics; vol 23, iss 1, 541; 1471-2105
Publication Year :
2022

Abstract

BackgroundLong-read shotgun metagenomic sequencing is gaining in popularity and offers many advantages over short-read sequencing. The higher information content in long reads is useful for a variety of metagenomics analyses, including taxonomic classification and profiling. The development of long-read specific tools for taxonomic classification is accelerating, yet there is a lack of information regarding their relative performance. Here, we perform a critical benchmarking study using 11 methods, including five methods designed specifically for long reads. We applied these tools to several mock community datasets generated using Pacific Biosciences (PacBio) HiFi or Oxford Nanopore Technology sequencing, and evaluated their performance based on read utilization, detection metrics, and relative abundance estimates.ResultsOur results show that long-read classifiers generally performed best. Several short-read classification and profiling methods produced many false positives (particularly at lower abundances), required heavy filtering to achieve acceptable precision (at the cost of reduced recall), and produced inaccurate abundance estimates. By contrast, two long-read methods (BugSeq, MEGAN-LR & DIAMOND) and one generalized method (sourmash) displayed high precision and recall without any filtering required. Furthermore, in the PacBio HiFi datasets these methods detected all species down to the 0.1% abundance level with high precision. Some long-read methods, such as MetaMaps and MMseqs2, required moderate filtering to reduce false positives to resemble the precision and recall of the top-performing methods. We found read quality affected performance for methods relying on protein prediction or exact k-mer matching, and these methods performed better with PacBio HiFi datasets. We also found that long-read datasets with a large proportion of shorter reads (< 2 kb length) resulted in lower precision and worse abundance estimates, relative to length-filtere

Details

Database :
OAIster
Journal :
BMC bioinformatics; vol 23, iss 1, 541; 1471-2105
Notes :
application/pdf, BMC bioinformatics vol 23, iss 1, 541 1471-2105
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391583996
Document Type :
Electronic Resource