BubbleGun: enumerating bubbles and superbubbles in genome graphs

Author:

Dabbaghie Fawaz12ORCID,Ebler Jana1,Marschall Tobias1ORCID

Affiliation:

1. Medical Faculty, Institute for Medical Biometry and Bioinformatics, Heinrich Heine University Düsseldorf , Düsseldorf 40225, Germany

2. Helmholtz Centre for Infection Research (HZI), Helmholtz Institute for Pharmaceutical Research Saarland (HIPS) , Saarbrücken 66123, Germany

Abstract

Abstract Motivation With the fast development of sequencing technology, accurate de novo genome assembly is now possible even for larger genomes. Graph-based representations of genomes arise both as part of the assembly process, but also in the context of pangenomes representing a population. In both cases, polymorphic loci lead to bubble structures in such graphs. Detecting bubbles is hence an important task when working with genomic variants in the context of genome graphs. Results Here, we present a fast general-purpose tool, called BubbleGun, for detecting bubbles and superbubbles in genome graphs. Furthermore, BubbleGun detects and outputs runs of linearly connected bubbles and superbubbles, which we call bubble chains. We showcase its utility on de Bruijn graphs and compare our results to vg’s snarl detection. We show that BubbleGun is considerably faster than vg especially in bigger graphs, where it reports all bubbles in less than 30 min on a human sample de Bruijn graph of around 2 million nodes. Availability and implementation BubbleGun is available and documented as a Python3 package at https://github.com/fawaz-dabbaghieh/bubble_gun under MIT license. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

German Federal Ministry for Research and Education

BMBF

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference16 articles.

1. A global reference for human genetic variation;1000 Genomes Project Consortium;Nature,2015

2. Compacting de Bruijn graphs from sequencing data quickly and in low memory;Chikhi;Bioinformatics,2016

3. Comparing variant call files for performance benchmarking of next-generation sequencing variant calling pipelines;Cleary;bioRxiv,2015

4. Computational pan-genomics: status, promises and challenges;Computational Pan-Genomics Consortium;Brief. Bioinform,2018

5. Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes;Ebler;Nat. Genet,2022

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3