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Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing()
In forensic genetics mitochondrial DNA (mtDNA) is usually analyzed by direct Sanger-type sequencing (STS). This method is known to be laborious and sometimes prone to human error. Alternative methods have been proposed that lead to faster results. Among these are methods that involve mass-spectromet...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820008/ https://www.ncbi.nlm.nih.gov/pubmed/24054029 http://dx.doi.org/10.1016/j.fsigen.2013.05.007 |
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author | Eduardoff, Mayra Huber, Gabriela Bayer, Birgit Schmid, Dagmar Anslinger, Katja Göbel, Tanja Zimmermann, Bettina Schneider, Peter M. Röck, Alexander W. Parson, Walther |
author_facet | Eduardoff, Mayra Huber, Gabriela Bayer, Birgit Schmid, Dagmar Anslinger, Katja Göbel, Tanja Zimmermann, Bettina Schneider, Peter M. Röck, Alexander W. Parson, Walther |
author_sort | Eduardoff, Mayra |
collection | PubMed |
description | In forensic genetics mitochondrial DNA (mtDNA) is usually analyzed by direct Sanger-type sequencing (STS). This method is known to be laborious and sometimes prone to human error. Alternative methods have been proposed that lead to faster results. Among these are methods that involve mass-spectrometry resulting in base composition profiles that are, by definition, less informative than the full nucleotide sequence. Here, we applied a highly automated electrospray ionization mass spectrometry (ESI-MS) system (PLEX-ID) to an mtDNA population study to compare its performance with respect to throughput and concordance to STS. We found that the loss of information power was relatively low compared to the gain in speed and analytical standardization. The detection of point and length heteroplasmy turned out to be roughly comparable between the technologies with some individual differences related to the processes. We confirm that ESI-MS provides a valuable platform for analyzing mtDNA variation that can also be applied in the forensic context. |
format | Online Article Text |
id | pubmed-3820008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38200082013-12-01 Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() Eduardoff, Mayra Huber, Gabriela Bayer, Birgit Schmid, Dagmar Anslinger, Katja Göbel, Tanja Zimmermann, Bettina Schneider, Peter M. Röck, Alexander W. Parson, Walther Forensic Sci Int Genet Article In forensic genetics mitochondrial DNA (mtDNA) is usually analyzed by direct Sanger-type sequencing (STS). This method is known to be laborious and sometimes prone to human error. Alternative methods have been proposed that lead to faster results. Among these are methods that involve mass-spectrometry resulting in base composition profiles that are, by definition, less informative than the full nucleotide sequence. Here, we applied a highly automated electrospray ionization mass spectrometry (ESI-MS) system (PLEX-ID) to an mtDNA population study to compare its performance with respect to throughput and concordance to STS. We found that the loss of information power was relatively low compared to the gain in speed and analytical standardization. The detection of point and length heteroplasmy turned out to be roughly comparable between the technologies with some individual differences related to the processes. We confirm that ESI-MS provides a valuable platform for analyzing mtDNA variation that can also be applied in the forensic context. Elsevier 2013-12 /pmc/articles/PMC3820008/ /pubmed/24054029 http://dx.doi.org/10.1016/j.fsigen.2013.05.007 Text en © 2013 The Authors https://creativecommons.org/licenses/by-nc-sa/3.0/ Open Access under CC BY-NC-SA 3.0 (https://creativecommons.org/licenses/by-nc-sa/3.0/) license |
spellingShingle | Article Eduardoff, Mayra Huber, Gabriela Bayer, Birgit Schmid, Dagmar Anslinger, Katja Göbel, Tanja Zimmermann, Bettina Schneider, Peter M. Röck, Alexander W. Parson, Walther Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title | Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title_full | Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title_fullStr | Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title_full_unstemmed | Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title_short | Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing() |
title_sort | mass spectrometric base composition profiling: implications for forensic mtdna databasing() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820008/ https://www.ncbi.nlm.nih.gov/pubmed/24054029 http://dx.doi.org/10.1016/j.fsigen.2013.05.007 |
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