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Multiplex STR amplification sensitivity in a silicon microchip

The demand for solutions to perform forensic DNA profiling outside of centralized laboratories is increasing. We here demonstrate highly sensitive STR amplification using a silicon micro-PCR (µPCR) chip. Exploiting industry-standard semiconductor manufacturing processes, a device was fabricated that...

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Autores principales: Cornelis, Senne, Fauvart, Maarten, Gansemans, Yannick, Vander Plaetsen, Ann-Sophie, Colle, Frederik, Wiederkehr, Rodrigo S., Deforce, Dieter, Stakenborg, Tim, Van Nieuwerburgh, Filip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026139/
https://www.ncbi.nlm.nih.gov/pubmed/29959383
http://dx.doi.org/10.1038/s41598-018-28229-9
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author Cornelis, Senne
Fauvart, Maarten
Gansemans, Yannick
Vander Plaetsen, Ann-Sophie
Colle, Frederik
Wiederkehr, Rodrigo S.
Deforce, Dieter
Stakenborg, Tim
Van Nieuwerburgh, Filip
author_facet Cornelis, Senne
Fauvart, Maarten
Gansemans, Yannick
Vander Plaetsen, Ann-Sophie
Colle, Frederik
Wiederkehr, Rodrigo S.
Deforce, Dieter
Stakenborg, Tim
Van Nieuwerburgh, Filip
author_sort Cornelis, Senne
collection PubMed
description The demand for solutions to perform forensic DNA profiling outside of centralized laboratories is increasing. We here demonstrate highly sensitive STR amplification using a silicon micro-PCR (µPCR) chip. Exploiting industry-standard semiconductor manufacturing processes, a device was fabricated that features a small form factor thanks to an integrated heating element covering three parallel micro-reactors with a reaction volume of 0.5 µl each. Diluted reference DNA samples (1 ng–31 pg) were amplified on the µPCR chip using the forensically validated AmpFISTR Identifier Plus kit, followed by conventional capillary electrophoresis. Complete STR profiles were generated with input DNA quantities down to 62 pg. Occasional allelic dropouts were observed from 31 pg downward. On-chip STR profiles were compared with those of identical samples amplified using a conventional thermal cycler for direct comparison of amplification sensitivity in a forensic setting. The observed sensitivity was in line with kit specifications for both µPCR and conventional PCR. Finally, a rapid amplification protocol was developed. Complete STR profiles could be generated in less than 17 minutes from as little as 125 pg template DNA. Together, our results are an important step towards the development of commercial, mass-produced, relatively cheap, handheld devices for on-site testing in forensic DNA analysis.
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spelling pubmed-60261392018-07-09 Multiplex STR amplification sensitivity in a silicon microchip Cornelis, Senne Fauvart, Maarten Gansemans, Yannick Vander Plaetsen, Ann-Sophie Colle, Frederik Wiederkehr, Rodrigo S. Deforce, Dieter Stakenborg, Tim Van Nieuwerburgh, Filip Sci Rep Article The demand for solutions to perform forensic DNA profiling outside of centralized laboratories is increasing. We here demonstrate highly sensitive STR amplification using a silicon micro-PCR (µPCR) chip. Exploiting industry-standard semiconductor manufacturing processes, a device was fabricated that features a small form factor thanks to an integrated heating element covering three parallel micro-reactors with a reaction volume of 0.5 µl each. Diluted reference DNA samples (1 ng–31 pg) were amplified on the µPCR chip using the forensically validated AmpFISTR Identifier Plus kit, followed by conventional capillary electrophoresis. Complete STR profiles were generated with input DNA quantities down to 62 pg. Occasional allelic dropouts were observed from 31 pg downward. On-chip STR profiles were compared with those of identical samples amplified using a conventional thermal cycler for direct comparison of amplification sensitivity in a forensic setting. The observed sensitivity was in line with kit specifications for both µPCR and conventional PCR. Finally, a rapid amplification protocol was developed. Complete STR profiles could be generated in less than 17 minutes from as little as 125 pg template DNA. Together, our results are an important step towards the development of commercial, mass-produced, relatively cheap, handheld devices for on-site testing in forensic DNA analysis. Nature Publishing Group UK 2018-06-29 /pmc/articles/PMC6026139/ /pubmed/29959383 http://dx.doi.org/10.1038/s41598-018-28229-9 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cornelis, Senne
Fauvart, Maarten
Gansemans, Yannick
Vander Plaetsen, Ann-Sophie
Colle, Frederik
Wiederkehr, Rodrigo S.
Deforce, Dieter
Stakenborg, Tim
Van Nieuwerburgh, Filip
Multiplex STR amplification sensitivity in a silicon microchip
title Multiplex STR amplification sensitivity in a silicon microchip
title_full Multiplex STR amplification sensitivity in a silicon microchip
title_fullStr Multiplex STR amplification sensitivity in a silicon microchip
title_full_unstemmed Multiplex STR amplification sensitivity in a silicon microchip
title_short Multiplex STR amplification sensitivity in a silicon microchip
title_sort multiplex str amplification sensitivity in a silicon microchip
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026139/
https://www.ncbi.nlm.nih.gov/pubmed/29959383
http://dx.doi.org/10.1038/s41598-018-28229-9
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