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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...

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Detalles Bibliográficos
Autores principales: Li, Wenzhou, Wypych, Jette, Duff, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
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.
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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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