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VIRUSBreakend: Viral Integration Recognition Using Single Breakends.


ABSTRACT:

Motivation

Integration of viruses into infected host cell DNA can cause DNA damage and disrupt genes. Recent cost reductions and growth of whole genome sequencing has produced a wealth of data in which viral presence and integration detection is possible. While key research and clinically relevant insights can be uncovered, existing software has not achieved widespread adoption, limited in part due to high computational costs, the inability to detect a wide range of viruses, as well as precision and sensitivity.

Results

Here, we describe VIRUSBreakend, a high-speed tool that identifies viral DNA presence and genomic integration. It utilizes single breakends, breakpoints in which only one side can be unambiguously placed, in a novel virus-centric variant calling and assembly approach to identify viral integrations with high sensitivity and a near-zero false discovery rate. VIRUSBreakend detects viral integrations anywhere in the host genome including regions such as centromeres and telomeres unable to be called by existing tools. Applying VIRUSBreakend to a large metastatic cancer cohort, we demonstrate that it can reliably detect clinically relevant viral presence and integration including HPV, HBV, MCPyV, EBV and HHV-8.

Availability and implementation

VIRUSBreakend is part of the Genomic Rearrangement IDentification Software Suite (GRIDSS). It is available under a GPLv3 license from https://github.com/PapenfussLab/VIRUSBreakend.

Supplementary information

Supplementary data are available at Bioinformatics online.

SUBMITTER: Cameron DL 

PROVIDER: S-EPMC8504616 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Publications

VIRUSBreakend: Viral Integration Recognition Using Single Breakends.

Cameron Daniel L DL   Jacobs Nina N   Roepman Paul P   Priestley Peter P   Cuppen Edwin E   Papenfuss Anthony T AT  

Bioinformatics (Oxford, England) 20211001 19


<h4>Motivation</h4>Integration of viruses into infected host cell DNA can cause DNA damage and disrupt genes. Recent cost reductions and growth of whole genome sequencing has produced a wealth of data in which viral presence and integration detection is possible. While key research and clinically relevant insights can be uncovered, existing software has not achieved widespread adoption, limited in part due to high computational costs, the inability to detect a wide range of viruses, as well as p  ...[more]

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