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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7802936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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