Performance of four modern whole genome amplification methods for copy number variant detection in single cells

Abstract Whole genome amplification (WGA) has become an invaluable tool to perform copy number variation (CNV) detection in single, or a limited number of cells. Unfortunately, current WGA methods introduce representation bias that limits the detection of small CNVs. New WGA methods have been introd...

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Autores principales: Lieselot Deleye, Laurentijn Tilleman, Ann-Sophie Vander Plaetsen, Senne Cornelis, Dieter Deforce, Filip Van Nieuwerburgh
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:914070b89b484e859bf641aa7e3176362021-12-02T12:31:47ZPerformance of four modern whole genome amplification methods for copy number variant detection in single cells10.1038/s41598-017-03711-y2045-2322https://doaj.org/article/914070b89b484e859bf641aa7e3176362017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03711-yhttps://doaj.org/toc/2045-2322Abstract Whole genome amplification (WGA) has become an invaluable tool to perform copy number variation (CNV) detection in single, or a limited number of cells. Unfortunately, current WGA methods introduce representation bias that limits the detection of small CNVs. New WGA methods have been introduced that might have the potential to reduce this bias. We compared the performance of PicoPLEX DNA-Seq (Picoseq), DOPlify, REPLI-g and Ampli-1 WGA for aneuploidy screening and copy number analysis using shallow whole genome massively parallel sequencing (MPS), starting from single or a limited number of cells. Although the four WGA methods perform differently, they are all suited for this application.Lieselot DeleyeLaurentijn TillemanAnn-Sophie Vander PlaetsenSenne CornelisDieter DeforceFilip Van NieuwerburghNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Lieselot Deleye
Laurentijn Tilleman
Ann-Sophie Vander Plaetsen
Senne Cornelis
Dieter Deforce
Filip Van Nieuwerburgh
Performance of four modern whole genome amplification methods for copy number variant detection in single cells
description Abstract Whole genome amplification (WGA) has become an invaluable tool to perform copy number variation (CNV) detection in single, or a limited number of cells. Unfortunately, current WGA methods introduce representation bias that limits the detection of small CNVs. New WGA methods have been introduced that might have the potential to reduce this bias. We compared the performance of PicoPLEX DNA-Seq (Picoseq), DOPlify, REPLI-g and Ampli-1 WGA for aneuploidy screening and copy number analysis using shallow whole genome massively parallel sequencing (MPS), starting from single or a limited number of cells. Although the four WGA methods perform differently, they are all suited for this application.
format article
author Lieselot Deleye
Laurentijn Tilleman
Ann-Sophie Vander Plaetsen
Senne Cornelis
Dieter Deforce
Filip Van Nieuwerburgh
author_facet Lieselot Deleye
Laurentijn Tilleman
Ann-Sophie Vander Plaetsen
Senne Cornelis
Dieter Deforce
Filip Van Nieuwerburgh
author_sort Lieselot Deleye
title Performance of four modern whole genome amplification methods for copy number variant detection in single cells
title_short Performance of four modern whole genome amplification methods for copy number variant detection in single cells
title_full Performance of four modern whole genome amplification methods for copy number variant detection in single cells
title_fullStr Performance of four modern whole genome amplification methods for copy number variant detection in single cells
title_full_unstemmed Performance of four modern whole genome amplification methods for copy number variant detection in single cells
title_sort performance of four modern whole genome amplification methods for copy number variant detection in single cells
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/914070b89b484e859bf641aa7e317636
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AT sennecornelis performanceoffourmodernwholegenomeamplificationmethodsforcopynumbervariantdetectioninsinglecells
AT dieterdeforce performanceoffourmodernwholegenomeamplificationmethodsforcopynumbervariantdetectioninsinglecells
AT filipvannieuwerburgh performanceoffourmodernwholegenomeamplificationmethodsforcopynumbervariantdetectioninsinglecells
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