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SummonChimera infers integrated viral genomes with nucleotide precision from NGS data
BACKGROUND: Viral integration into a host genome is defined by two chimeric junctions that join viral and host DNA. Recently, computational tools have been developed that utilize NGS data to detect chimeric junctions. These methods identify individual viral-host junctions but do not associate chimer...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210586/ https://www.ncbi.nlm.nih.gov/pubmed/25331652 http://dx.doi.org/10.1186/s12859-014-0348-4 |
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author | Katz, Joshua P Pipas, James M |
author_facet | Katz, Joshua P Pipas, James M |
author_sort | Katz, Joshua P |
collection | PubMed |
description | BACKGROUND: Viral integration into a host genome is defined by two chimeric junctions that join viral and host DNA. Recently, computational tools have been developed that utilize NGS data to detect chimeric junctions. These methods identify individual viral-host junctions but do not associate chimeric pairs as an integration event. Without knowing the chimeric boundaries of an integration, its genetic content cannot be determined. RESULTS: Summonchimera is a Perl program that associates chimera pairs to infer the complete viral genomic integration event to the nucleotide level within single or paired-end NGS data. SummonChimera integration prediction was verified on a set of single-end IonTorrent reads from a purified Salmonella bacterium with an integrated bacteriophage. Furthermore, SummonChimera predicted integrations from experimentally verified Hepatitis B Virus chimeras within a paired-end Whole Genome Sequencing hepatocellular carcinoma tumor database. CONCLUSIONS: SummonChimera identified all experimentally verified chimeras detected by current computational methods. Further, SummonChimera integration inference precisely predicted bacteriophage integration. The application of SummonChimera to cancer NGS accurately identifies deletion of host and viral sequence during integration. The precise nucleotide determination of an integration allows prediction of viral and cellular gene transcription patterns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0348-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4210586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42105862014-10-29 SummonChimera infers integrated viral genomes with nucleotide precision from NGS data Katz, Joshua P Pipas, James M BMC Bioinformatics Software BACKGROUND: Viral integration into a host genome is defined by two chimeric junctions that join viral and host DNA. Recently, computational tools have been developed that utilize NGS data to detect chimeric junctions. These methods identify individual viral-host junctions but do not associate chimeric pairs as an integration event. Without knowing the chimeric boundaries of an integration, its genetic content cannot be determined. RESULTS: Summonchimera is a Perl program that associates chimera pairs to infer the complete viral genomic integration event to the nucleotide level within single or paired-end NGS data. SummonChimera integration prediction was verified on a set of single-end IonTorrent reads from a purified Salmonella bacterium with an integrated bacteriophage. Furthermore, SummonChimera predicted integrations from experimentally verified Hepatitis B Virus chimeras within a paired-end Whole Genome Sequencing hepatocellular carcinoma tumor database. CONCLUSIONS: SummonChimera identified all experimentally verified chimeras detected by current computational methods. Further, SummonChimera integration inference precisely predicted bacteriophage integration. The application of SummonChimera to cancer NGS accurately identifies deletion of host and viral sequence during integration. The precise nucleotide determination of an integration allows prediction of viral and cellular gene transcription patterns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0348-4) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-22 /pmc/articles/PMC4210586/ /pubmed/25331652 http://dx.doi.org/10.1186/s12859-014-0348-4 Text en © Katz and Pipas; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Software Katz, Joshua P Pipas, James M SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title | SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title_full | SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title_fullStr | SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title_full_unstemmed | SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title_short | SummonChimera infers integrated viral genomes with nucleotide precision from NGS data |
title_sort | summonchimera infers integrated viral genomes with nucleotide precision from ngs data |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210586/ https://www.ncbi.nlm.nih.gov/pubmed/25331652 http://dx.doi.org/10.1186/s12859-014-0348-4 |
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