NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions.
Codon
Escherichia coli O157
/ genetics
Exons
Genes, Bacterial
Genes, Viral
High-Throughput Nucleotide Sequencing
/ methods
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
/ genetics
Listeria monocytogenes
/ genetics
Multiplex Polymerase Chain Reaction
/ methods
Nucleic Acid Hybridization
Polymorphism, Single Nucleotide
Staphylococcus aureus
/ genetics
Viruses
/ genetics
Journal
PLoS computational biology
ISSN: 1553-7358
Titre abrégé: PLoS Comput Biol
Pays: United States
ID NLM: 101238922
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
02
07
2020
accepted:
24
10
2020
revised:
12
01
2021
pubmed:
31
12
2020
medline:
20
2
2021
entrez:
30
12
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33378360
doi: 10.1371/journal.pcbi.1008468
pii: PCOMPBIOL-D-20-01153
pmc: PMC7802936
doi:
Substances chimiques
Codon
0
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
EC 2.7.11.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1008468Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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