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NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions

Multiplex polymerase chain reaction (PCR) has multiple applications in molecular biology, including developing new targeted next-generation sequencing (NGS) panels. We present NGS-PrimerPlex, an efficient and versatile command-line application that designs primers for different refined types of ampl...

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Autores principales: Kechin, Andrey, Borobova, Viktoria, Boyarskikh, Ulyana, Khrapov, Evgeniy, Subbotin, Sergey, Filipenko, Maxim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802936/
https://www.ncbi.nlm.nih.gov/pubmed/33378360
http://dx.doi.org/10.1371/journal.pcbi.1008468
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author Kechin, Andrey
Borobova, Viktoria
Boyarskikh, Ulyana
Khrapov, Evgeniy
Subbotin, Sergey
Filipenko, Maxim
author_facet Kechin, Andrey
Borobova, Viktoria
Boyarskikh, Ulyana
Khrapov, Evgeniy
Subbotin, Sergey
Filipenko, Maxim
author_sort Kechin, Andrey
collection PubMed
description Multiplex polymerase chain reaction (PCR) has multiple applications in molecular biology, including developing new targeted next-generation sequencing (NGS) panels. We present NGS-PrimerPlex, an efficient and versatile command-line application that designs primers for different refined types of amplicon-based genome target enrichment. It supports nested and anchored multiplex PCR, redistribution among multiplex reactions of primers constructed earlier, and extension of existing NGS-panels. The primer design process takes into consideration the formation of secondary structures, non-target amplicons between all primers of a pool, primers and high-frequent genome single-nucleotide polymorphisms (SNPs) overlapping. Moreover, users of NGS-PrimerPlex are free from manually defining input genome regions, because it can be done automatically from a list of genes or their parts like exon or codon numbers. Using the program, the NGS-panel for sequencing the LRRK2 gene coding regions was created, and 354 DNA samples were studied successfully with a median coverage of 97.4% of target regions by at least 30 reads. To show that NGS-PrimerPlex can also be applied for bacterial genomes, we designed primers to detect foodborne pathogens Salmonella enterica, Escherichia coli O157:H7, Listeria monocytogenes, and Staphylococcus aureus considering variable positions of the genomes.
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spelling pubmed-78029362021-01-22 NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions Kechin, Andrey Borobova, Viktoria Boyarskikh, Ulyana Khrapov, Evgeniy Subbotin, Sergey Filipenko, Maxim PLoS Comput Biol Research Article Multiplex polymerase chain reaction (PCR) has multiple applications in molecular biology, including developing new targeted next-generation sequencing (NGS) panels. We present NGS-PrimerPlex, an efficient and versatile command-line application that designs primers for different refined types of amplicon-based genome target enrichment. It supports nested and anchored multiplex PCR, redistribution among multiplex reactions of primers constructed earlier, and extension of existing NGS-panels. The primer design process takes into consideration the formation of secondary structures, non-target amplicons between all primers of a pool, primers and high-frequent genome single-nucleotide polymorphisms (SNPs) overlapping. Moreover, users of NGS-PrimerPlex are free from manually defining input genome regions, because it can be done automatically from a list of genes or their parts like exon or codon numbers. Using the program, the NGS-panel for sequencing the LRRK2 gene coding regions was created, and 354 DNA samples were studied successfully with a median coverage of 97.4% of target regions by at least 30 reads. To show that NGS-PrimerPlex can also be applied for bacterial genomes, we designed primers to detect foodborne pathogens Salmonella enterica, Escherichia coli O157:H7, Listeria monocytogenes, and Staphylococcus aureus considering variable positions of the genomes. Public Library of Science 2020-12-30 /pmc/articles/PMC7802936/ /pubmed/33378360 http://dx.doi.org/10.1371/journal.pcbi.1008468 Text en © 2020 Kechin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kechin, Andrey
Borobova, Viktoria
Boyarskikh, Ulyana
Khrapov, Evgeniy
Subbotin, Sergey
Filipenko, Maxim
NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title_full NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title_fullStr NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title_full_unstemmed NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title_short NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions
title_sort ngs-primerplex: high-throughput primer design for multiplex polymerase chain reactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802936/
https://www.ncbi.nlm.nih.gov/pubmed/33378360
http://dx.doi.org/10.1371/journal.pcbi.1008468
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