File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Conference Paper: MegaPath-Nano: Accurate Compositional Analysis and Drug-level Antimicrobial Resistance Detection Software for Oxford Nanopore Long-read Metagenomics

TitleMegaPath-Nano: Accurate Compositional Analysis and Drug-level Antimicrobial Resistance Detection Software for Oxford Nanopore Long-read Metagenomics
Authors
Keywordspathogen detection
antimicrobial resistance prediction
MinION long reads
metagenomics
compositional analysis
Issue Date2020
PublisherIEEE. The Journal's web site is located at http://ieeexplore.ieee.org/xpl/conhome.jsp?punumber=1001586
Citation
Proceedings of IEEE International Conference on Bioinformatics and Biomedicine 2020 (IEEE BIBM 2020), Virtual Conference, Seoul, Korea, 16-19 December 2020, p. 329-336 How to Cite?
AbstractAccurate and sensitive taxonomic profiling is essential for any metagenomic analysis for revealing microbial community structure and for potential functional prediction. Antimicrobial resistance (AMR) detection is also a critical task in the clinical diagnosis of infection and antimicrobial therapy. By incorporating Oxford Nanopore Technologies (ONT) sequencing, users benefit from the high-confidence alignment of long reads for taxonomic classification, even among bacteria with similar genomes. Portable ONT devices, such as VolTRAX with MinION, allow short turnaround time for detection and can be used in a lightweight laboratory setting. However, error-prone ONT sequencing reads are still challenging for existing software for accurate taxonomic classification of microbes and detection of AMR down to the drug level. In this paper, we present MegaPath-Nano, the successor to NGS-based MegaPath. It is a high-precision compositional analysis software with drug-level AMR detection for ONT metagenomic sequencing data. MegaPath-Nano performs 1) thorough multi-level filtering against decoy and human reads, while removing noisy alignments, 2) alignment-based taxonomic classification with RefSeq down to strain-level, with an alignment-reassignment algorithm to tackle the challenge of non-unique alignments, based on global alignment distribution, and 3) comprehensive downstream drug-level AMR detection, integrating five AMR databases. In our benchmarks using the Zymo metagenomic datasets, MegaPath-Nano performed better than other existing software for taxonomic classification. We also sequenced five real patient isolates using MinION to benchmark the performance of AMR detection. MegaPath-Nano was the most accurate and provided the most comprehensive output at both the drug and class level of AMR prediction against other state-of-the-art software. MegaPath-Nano is open-source and available at https://github.com/HKU-BAL/MegaPath-Nano.
Persistent Identifierhttp://hdl.handle.net/10722/301413
ISBN

 

DC FieldValueLanguage
dc.contributor.authorLui, WW-
dc.contributor.authorLeung, WS-
dc.contributor.authorLeung, HCM-
dc.contributor.authorXin, Y-
dc.contributor.authorTeng, LL-
dc.contributor.authorWoo, PCY-
dc.contributor.authorLam, TW-
dc.contributor.authorLuo, R-
dc.date.accessioned2021-07-27T08:10:42Z-
dc.date.available2021-07-27T08:10:42Z-
dc.date.issued2020-
dc.identifier.citationProceedings of IEEE International Conference on Bioinformatics and Biomedicine 2020 (IEEE BIBM 2020), Virtual Conference, Seoul, Korea, 16-19 December 2020, p. 329-336-
dc.identifier.isbn9781728162164-
dc.identifier.urihttp://hdl.handle.net/10722/301413-
dc.description.abstractAccurate and sensitive taxonomic profiling is essential for any metagenomic analysis for revealing microbial community structure and for potential functional prediction. Antimicrobial resistance (AMR) detection is also a critical task in the clinical diagnosis of infection and antimicrobial therapy. By incorporating Oxford Nanopore Technologies (ONT) sequencing, users benefit from the high-confidence alignment of long reads for taxonomic classification, even among bacteria with similar genomes. Portable ONT devices, such as VolTRAX with MinION, allow short turnaround time for detection and can be used in a lightweight laboratory setting. However, error-prone ONT sequencing reads are still challenging for existing software for accurate taxonomic classification of microbes and detection of AMR down to the drug level. In this paper, we present MegaPath-Nano, the successor to NGS-based MegaPath. It is a high-precision compositional analysis software with drug-level AMR detection for ONT metagenomic sequencing data. MegaPath-Nano performs 1) thorough multi-level filtering against decoy and human reads, while removing noisy alignments, 2) alignment-based taxonomic classification with RefSeq down to strain-level, with an alignment-reassignment algorithm to tackle the challenge of non-unique alignments, based on global alignment distribution, and 3) comprehensive downstream drug-level AMR detection, integrating five AMR databases. In our benchmarks using the Zymo metagenomic datasets, MegaPath-Nano performed better than other existing software for taxonomic classification. We also sequenced five real patient isolates using MinION to benchmark the performance of AMR detection. MegaPath-Nano was the most accurate and provided the most comprehensive output at both the drug and class level of AMR prediction against other state-of-the-art software. MegaPath-Nano is open-source and available at https://github.com/HKU-BAL/MegaPath-Nano.-
dc.languageeng-
dc.publisherIEEE. The Journal's web site is located at http://ieeexplore.ieee.org/xpl/conhome.jsp?punumber=1001586-
dc.relation.ispartofIEEE International Conference on Bioinformatics and Biomedicine Proceedings-
dc.rightsIEEE International Conference on Bioinformatics and Biomedicine Proceedings. Copyright © IEEE.-
dc.rights©2020 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works.-
dc.subjectpathogen detection-
dc.subjectantimicrobial resistance prediction-
dc.subjectMinION long reads-
dc.subjectmetagenomics-
dc.subjectcompositional analysis-
dc.titleMegaPath-Nano: Accurate Compositional Analysis and Drug-level Antimicrobial Resistance Detection Software for Oxford Nanopore Long-read Metagenomics-
dc.typeConference_Paper-
dc.identifier.emailLeung, WS: amywingsze@connect.hku.hk-
dc.identifier.emailTeng, LL: llteng@hku.hk-
dc.identifier.emailLam, TW: twlam@cs.hku.hk-
dc.identifier.emailLuo, R: rbluo@cs.hku.hk-
dc.identifier.authorityLeung, HCM=rp00144-
dc.identifier.authorityTeng, LL=rp00277-
dc.identifier.authorityWoo, PCY=rp00430-
dc.identifier.authorityLam, TW=rp00135-
dc.identifier.authorityLuo, R=rp02360-
dc.description.naturepostprint-
dc.identifier.doi10.1109/BIBM49941.2020.9313313-
dc.identifier.scopuseid_2-s2.0-85100343310-
dc.identifier.hkuros323498-
dc.identifier.spage329-
dc.identifier.epage336-
dc.publisher.placeUnited States-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats