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Biology subjects

Heath, L.

Publications and source records attributed to Heath, L..

2 recordsLinked to original sources

ARG-miner: A web platform for crowdsourcing-based curation of antibiotic resistance genes

Curation of antibiotic resistance gene (ARG) databases is a labor-intensive process that requires expert knowledge to manually collect, correct, and/or annotate individual genes. Correspondingly, updates to existing databases tend to be infrequent, commonly requiring years for completion and often containing inconsistences. Further, because of limitations of manual curation, most existing ARG databases contain only a small proportion of known ARGs (~5k genes). A new approach is needed to achieve a truly comprehensive ARG database, while also maintaining a high level of accuracy. Here we propose a new web-based curation system, ARG-miner, which supports annotation of ARGs at multiple levels, including: gene name, antibiotic category, resistance mechanism, and evidence for mobility and occurrence in clinically-important bacterial strains. To overcome limitations of manual curation, we employ crowdsourcing as a novel strategy for expanding curation capacity towards achieving a truly comprehensive, up-to-date database. We develop and validate the approach by comparing performance of multiple cohorts of curators with varying levels of expertise, demonstrating that ARG-miner is more cost effective and less time-consuming relative to traditional expert curation. We further demonstrate the reliability of a trust validation filter for rejecting confounding input generated by spammers. Crowdsourcing was found to be as accurate as expert annotation, with an accuracy >90% for the annotation of a diverse test set of ARGs. ARG-miner provides a public API and database available at http://bench.cs.vt.edu/argminer.

bioinformatics

Panaconda: Application of pan-synteny graph models to genome content analysis

MotivationWhole-genome alignment and pan-genome analysis are useful tools in understanding the similarities and differences of many genomes in an evolutionary context. Here we introduce the concept of pan-synteny graphs, an analysis method that combines elements of both to represent conservation and change of multiple prokaryotic genomes at an architectural level. Pan-synteny graphs represent a reference free approach for the comparison of many genomes and allows for the identification of synteny, insertion, deletion, replacement, inversion, recombination, missed assembly joins, evolutionary hotspots, and reference based scaffolding.\n\nResultsWe present an algorithm for creating whole genome multiple sequence comparisons and a model for representing the similarities and differences among sequences as a graph of syntenic gene families. As part of the pan-synteny graph creation, we first create a de Bruijn graph. Instead of the alphabet of nucleotides commonly used in genome assembly, we use an alphabet of gene families. This de Bruijn graph is then processed to create the pan-synteny graph. Our approach is novel in that it explicitly controls how regions from the same sequence and genome are aligned and generates a graph in which all sequences are fully represented as paths. This method harnesses previous computation involved in protein family calculation to speed up the creation of whole genome alignment for many genomes. We provide the software suite Panaconda, for the calculation of pan-synteny graphs given annotation input, and an implementation of methods for their layout and visualization.\n\nAvailabilityPanaconda is available at https://github.com/aswarren/pangenome_graphs and datasets used in examples are available at https://github.com/aswarren/pangenome_examples\n\nContactAndrew Warren anwarren@vt.edu

bioinformatics