Cargando…
Using HPV-meta for human papillomavirus RNA quality detection
In the era of cervical cancer elimination, accurate and validated pipelines to detect human papillomavirus are essential to elucidate and understand HPV association with human cancers. We aimed to provide an open-source pipeline, “HPV-meta”, to detect HPV transcripts in RNA sequencing data, includin...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338075/ https://www.ncbi.nlm.nih.gov/pubmed/35906372 http://dx.doi.org/10.1038/s41598-022-17318-5 |
_version_ | 1784759888729079808 |
---|---|
author | Ure, Agustin Mukhedkar, Dhananjay Arroyo Mühr, Laila Sara |
author_facet | Ure, Agustin Mukhedkar, Dhananjay Arroyo Mühr, Laila Sara |
author_sort | Ure, Agustin |
collection | PubMed |
description | In the era of cervical cancer elimination, accurate and validated pipelines to detect human papillomavirus are essential to elucidate and understand HPV association with human cancers. We aimed to provide an open-source pipeline, “HPV-meta”, to detect HPV transcripts in RNA sequencing data, including several steps to warn operators for possible viral contamination. The “HPV-meta” pipeline automatically performs several steps, starting with quality trimming, human genome filtering, HPV detection (blastx), cut-off settlement (10 reads and 690 bp coverage to make an HPV call) and finishing with fasta sequence generation for HPV positive samples. Fasta sequences can then be aligned to assess sequence diversity among HPV positive samples. All RNA sequencing files (n = 10,908) present in the cancer genome atlas (TCGA) were analyzed. “HPV-meta” identified 25 different HPV types being present in 488/10,904 specimens. Validation of results showed 99.98% agreement (10,902/10,904). Multiple alignment from fasta files warned about high sequence identity between several HPV 18 and 38 positive samples, whose contamination had previously been reported. The “HPV-meta” pipeline is a robust and validated pipeline that detects HPV in RNA sequencing data. Obtaining the fasta files enables contamination investigation, a non very rare occurrence in next generation sequencing. |
format | Online Article Text |
id | pubmed-9338075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93380752022-07-31 Using HPV-meta for human papillomavirus RNA quality detection Ure, Agustin Mukhedkar, Dhananjay Arroyo Mühr, Laila Sara Sci Rep Article In the era of cervical cancer elimination, accurate and validated pipelines to detect human papillomavirus are essential to elucidate and understand HPV association with human cancers. We aimed to provide an open-source pipeline, “HPV-meta”, to detect HPV transcripts in RNA sequencing data, including several steps to warn operators for possible viral contamination. The “HPV-meta” pipeline automatically performs several steps, starting with quality trimming, human genome filtering, HPV detection (blastx), cut-off settlement (10 reads and 690 bp coverage to make an HPV call) and finishing with fasta sequence generation for HPV positive samples. Fasta sequences can then be aligned to assess sequence diversity among HPV positive samples. All RNA sequencing files (n = 10,908) present in the cancer genome atlas (TCGA) were analyzed. “HPV-meta” identified 25 different HPV types being present in 488/10,904 specimens. Validation of results showed 99.98% agreement (10,902/10,904). Multiple alignment from fasta files warned about high sequence identity between several HPV 18 and 38 positive samples, whose contamination had previously been reported. The “HPV-meta” pipeline is a robust and validated pipeline that detects HPV in RNA sequencing data. Obtaining the fasta files enables contamination investigation, a non very rare occurrence in next generation sequencing. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9338075/ /pubmed/35906372 http://dx.doi.org/10.1038/s41598-022-17318-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ure, Agustin Mukhedkar, Dhananjay Arroyo Mühr, Laila Sara Using HPV-meta for human papillomavirus RNA quality detection |
title | Using HPV-meta for human papillomavirus RNA quality detection |
title_full | Using HPV-meta for human papillomavirus RNA quality detection |
title_fullStr | Using HPV-meta for human papillomavirus RNA quality detection |
title_full_unstemmed | Using HPV-meta for human papillomavirus RNA quality detection |
title_short | Using HPV-meta for human papillomavirus RNA quality detection |
title_sort | using hpv-meta for human papillomavirus rna quality detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338075/ https://www.ncbi.nlm.nih.gov/pubmed/35906372 http://dx.doi.org/10.1038/s41598-022-17318-5 |
work_keys_str_mv | AT ureagustin usinghpvmetaforhumanpapillomavirusrnaqualitydetection AT mukhedkardhananjay usinghpvmetaforhumanpapillomavirusrnaqualitydetection AT arroyomuhrlailasara usinghpvmetaforhumanpapillomavirusrnaqualitydetection |