PRAWNS: compact pan-genomic features for whole-genome population genomics

被引:1
作者
Javkar, Kiran [1 ,2 ]
Rand, Hugh [3 ]
Strain, Errol [4 ]
Pop, Mihai [1 ]
机构
[1] Univ Maryland, Dept Comp Sci, College Pk, MD 20742 USA
[2] Univ Maryland, Joint Inst Food Safety & Appl Nutr, College Pk, MD 20740 USA
[3] US FDA, Ctr Food Safety & Appl Nutr, College Pk, MD 20740 USA
[4] US FDA, Ctr Vet Med, Laurel, MD 20708 USA
基金
美国国家卫生研究院;
关键词
ANTIBIOTIC-RESISTANCE; MULTIPLE ALIGNMENT; ALGORITHM; SEQUENCE;
D O I
10.1093/bioinformatics/btac844
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Scientists seeking to understand the genomic basis of bacterial phenotypes, such as antibiotic resistance, today have access to an unprecedented number of complete and nearly complete genomes. Making sense of these data requires computational tools able to perform multiple-genome comparisons efficiently, yet currently available tools cannot scale beyond several tens of genomes. Results: We describe PRAWNS, an efficient and scalable tool for multiple-genome analysis. PRAWNS defines a concise set of genomic features (metablocks), as well as pairwise relationships between them, which can be used as a basis for large-scale genotype-phenotype association studies. We demonstrate the effectiveness of PRAWNS by identifying genomic regions associated with antibiotic resistance in Acinetobacter baumannii. Availability and implementation: PRAWNS is implemented in C++ and Python3, licensed under the GPLv3 license, and freely downloadable from GitHub (https://github.com/KiranJavkar/PRAWNS.git). Contact: mpop@umd.edu Supplementary information: Supplementary data are available at Bioinformatics online.
引用
收藏
页数:8
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