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Improved sequence variant analysis strategy by automated false positive removal
Sequence variant analysis (SVA) is critical in therapeutic protein development because it ensures the absence of genetic mutations of a production clone or high-level misincorporations during cell culture. While software for searching sequence variants from mass spectrometry data are available, effe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540081/ https://www.ncbi.nlm.nih.gov/pubmed/28590201 http://dx.doi.org/10.1080/19420862.2017.1336591 |
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author | Li, Wenzhou Wypych, Jette Duff, Robert J. |
author_facet | Li, Wenzhou Wypych, Jette Duff, Robert J. |
author_sort | Li, Wenzhou |
collection | PubMed |
description | Sequence variant analysis (SVA) is critical in therapeutic protein development because it ensures the absence of genetic mutations of a production clone or high-level misincorporations during cell culture. While software for searching sequence variants from mass spectrometry data are available, effectively distinguishing true positives from a large number of false positives in the reported hits or identifications found in the error tolerant search mode is a challenge. This verification process must be done manually and can take several days or even weeks to accomplish. We report here the use of a Perl-based script to evaluate every identified hit to remove the false positives from the search results of PepFinder™ (also known as MassAnalyzer) based on orthogonal criteria. Our data show that the false positives from PepFinder™ output were reduced ∼4-fold without loss of accuracy in the detection of true identifications, representing a more than 70% reduction in time compared with the manual data verification process. |
format | Online Article Text |
id | pubmed-5540081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-55400812017-09-01 Improved sequence variant analysis strategy by automated false positive removal Li, Wenzhou Wypych, Jette Duff, Robert J. MAbs Report Sequence variant analysis (SVA) is critical in therapeutic protein development because it ensures the absence of genetic mutations of a production clone or high-level misincorporations during cell culture. While software for searching sequence variants from mass spectrometry data are available, effectively distinguishing true positives from a large number of false positives in the reported hits or identifications found in the error tolerant search mode is a challenge. This verification process must be done manually and can take several days or even weeks to accomplish. We report here the use of a Perl-based script to evaluate every identified hit to remove the false positives from the search results of PepFinder™ (also known as MassAnalyzer) based on orthogonal criteria. Our data show that the false positives from PepFinder™ output were reduced ∼4-fold without loss of accuracy in the detection of true identifications, representing a more than 70% reduction in time compared with the manual data verification process. Taylor & Francis 2017-06-07 /pmc/articles/PMC5540081/ /pubmed/28590201 http://dx.doi.org/10.1080/19420862.2017.1336591 Text en © 2017 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Report Li, Wenzhou Wypych, Jette Duff, Robert J. Improved sequence variant analysis strategy by automated false positive removal |
title | Improved sequence variant analysis strategy by automated false positive removal |
title_full | Improved sequence variant analysis strategy by automated false positive removal |
title_fullStr | Improved sequence variant analysis strategy by automated false positive removal |
title_full_unstemmed | Improved sequence variant analysis strategy by automated false positive removal |
title_short | Improved sequence variant analysis strategy by automated false positive removal |
title_sort | improved sequence variant analysis strategy by automated false positive removal |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540081/ https://www.ncbi.nlm.nih.gov/pubmed/28590201 http://dx.doi.org/10.1080/19420862.2017.1336591 |
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