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Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data
Motivation: CYP2D6 is highly polymorphic gene which encodes the (CYP2D6) enzyme, involved in the metabolism of 20–25% of all clinically prescribed drugs and other xenobiotics in the human body. CYP2D6 genotyping is recommended prior to treatment decisions involving one or more of the numerous drugs...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542776/ https://www.ncbi.nlm.nih.gov/pubmed/26072492 http://dx.doi.org/10.1093/bioinformatics/btv232 |
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author | Numanagić, Ibrahim Malikić, Salem Pratt, Victoria M. Skaar, Todd C. Flockhart, David A. Sahinalp, S. Cenk |
author_facet | Numanagić, Ibrahim Malikić, Salem Pratt, Victoria M. Skaar, Todd C. Flockhart, David A. Sahinalp, S. Cenk |
author_sort | Numanagić, Ibrahim |
collection | PubMed |
description | Motivation: CYP2D6 is highly polymorphic gene which encodes the (CYP2D6) enzyme, involved in the metabolism of 20–25% of all clinically prescribed drugs and other xenobiotics in the human body. CYP2D6 genotyping is recommended prior to treatment decisions involving one or more of the numerous drugs sensitive to CYP2D6 allelic composition. In this context, high-throughput sequencing (HTS) technologies provide a promising time-efficient and cost-effective alternative to currently used genotyping techniques. To achieve accurate interpretation of HTS data, however, one needs to overcome several obstacles such as high sequence similarity and genetic recombinations between CYP2D6 and evolutionarily related pseudogenes CYP2D7 and CYP2D8, high copy number variation among individuals and short read lengths generated by HTS technologies. Results: In this work, we present the first algorithm to computationally infer CYP2D6 genotype at basepair resolution from HTS data. Our algorithm is able to resolve complex genotypes, including alleles that are the products of duplication, deletion and fusion events involving CYP2D6 and its evolutionarily related cousin CYP2D7. Through extensive experiments using simulated and real datasets, we show that our algorithm accurately solves this important problem with potential clinical implications. Availability and implementation: Cypiripi is available at http://sfu-compbio.github.io/cypiripi. Contact: cenk@sfu.ca. |
format | Online Article Text |
id | pubmed-4542776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45427762015-08-25 Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data Numanagić, Ibrahim Malikić, Salem Pratt, Victoria M. Skaar, Todd C. Flockhart, David A. Sahinalp, S. Cenk Bioinformatics Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Motivation: CYP2D6 is highly polymorphic gene which encodes the (CYP2D6) enzyme, involved in the metabolism of 20–25% of all clinically prescribed drugs and other xenobiotics in the human body. CYP2D6 genotyping is recommended prior to treatment decisions involving one or more of the numerous drugs sensitive to CYP2D6 allelic composition. In this context, high-throughput sequencing (HTS) technologies provide a promising time-efficient and cost-effective alternative to currently used genotyping techniques. To achieve accurate interpretation of HTS data, however, one needs to overcome several obstacles such as high sequence similarity and genetic recombinations between CYP2D6 and evolutionarily related pseudogenes CYP2D7 and CYP2D8, high copy number variation among individuals and short read lengths generated by HTS technologies. Results: In this work, we present the first algorithm to computationally infer CYP2D6 genotype at basepair resolution from HTS data. Our algorithm is able to resolve complex genotypes, including alleles that are the products of duplication, deletion and fusion events involving CYP2D6 and its evolutionarily related cousin CYP2D7. Through extensive experiments using simulated and real datasets, we show that our algorithm accurately solves this important problem with potential clinical implications. Availability and implementation: Cypiripi is available at http://sfu-compbio.github.io/cypiripi. Contact: cenk@sfu.ca. Oxford University Press 2015-06-15 2015-06-10 /pmc/articles/PMC4542776/ /pubmed/26072492 http://dx.doi.org/10.1093/bioinformatics/btv232 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License(http://creativecommons.org/licenses/by-nc/3.0/),which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Numanagić, Ibrahim Malikić, Salem Pratt, Victoria M. Skaar, Todd C. Flockhart, David A. Sahinalp, S. Cenk Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title | Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title_full | Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title_fullStr | Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title_full_unstemmed | Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title_short | Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data |
title_sort | cypiripi: exact genotyping of cyp2d6 using high-throughput sequencing data |
topic | Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542776/ https://www.ncbi.nlm.nih.gov/pubmed/26072492 http://dx.doi.org/10.1093/bioinformatics/btv232 |
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