Publication: Integrated minimum-set primers and unique probe design algorithms for differential detection on symptom-related pathogens
cris.lastimport.scopus | 2025-05-05T22:14:37Z | |
cris.virtual.department | Plant Pathology and Microbiology | en_US |
cris.virtual.orcid | 0000-0002-7564-0956 | en_US |
cris.virtualsource.department | d4183095-e98d-4d34-8105-d70f5345f1df | |
cris.virtualsource.orcid | d4183095-e98d-4d34-8105-d70f5345f1df | |
dc.contributor.author | Huang, Yu-Cheng | en_US |
dc.contributor.author | Chang, Chun-Fan | en_US |
dc.contributor.author | Chan, Chen-hsiung | en_US |
dc.contributor.author | Yeh, Tze-Jung | en_US |
dc.contributor.author | YA-CHUN CHANG | en_US |
dc.contributor.author | Chen, Chaur-Chin | en_US |
dc.contributor.author | Kao, Cheng-Yan | en_US |
dc.creator | Huang, Yu-Cheng; Chang, Chun-Fan; Chan, Chen-Hsiung; Yeh, Tze-Jung; Chang, Ya-Chun; Chen, Chaur-Chin; Kao, Cheng-Yan | |
dc.date.accessioned | 2018-09-10T05:17:05Z | |
dc.date.available | 2018-09-10T05:17:05Z | |
dc.date.issued | 2005 | |
dc.description.abstract | Motivation: Differential detection on symptom-related pathogens (SRP) is critical for fast identification and accurate control against epidemic diseases. Conventional polymerase chain reaction (PCR) requires a large number of unique primers to amplify selected SRP target sequences. With multiple-use primers (mu-primers), multiple targets can be amplified and detected in one PCR experiment under standard reaction condition and reduced detection complexity. However, the time complexity of designing mu-primers with the best heuristic method available is too vast. We have formulated minimum-set mu-primer design problem as a set covering problem (SCP), and used modified compact genetic algorithm (MCGA) to solve this problem optimally and efficiently. We have also proposed new strategies of primer/probe design algorithm (PDA) on combining both minimum-set (MS) mu-primers and unique (UniQ) probes. Designed primer/ probe set by PDA-MS/UniQ can amplify multiple genes simultaneously upon physical presence with minimum-set mu-primer amplification (MMA) before intended differential detection with probes-array hybridization (PAH) on the selected target set of SRP. Results: The proposed PDA-MS/UniQ metho d pursues a much smaller number of primers set compared with conventional PCR. In the simulation experiment for amplifying 12669 target sequences, the performance of our method with 68% reduction on required mu-primers number seems to be superior to the compared heuristic approaches in both computation efficiency and reduction percentage. Our integrated PDA-MS/UniQ method is applied to the differential detection on 9 plant viruses from 4 genera with MMA and PAH of 11 mu-primers instead of 18 unique ones in conventional PCR while amplifying overall 9 target sequences. The results of wet lab experiments with integrated MMA-PAH system have successfully validated the specificity and sensitivity of the primers/ probes designed with our integrated PDA-MS/UniQ method. ? The Author 2005. Published by Oxford University Press. All rights reserved. | |
dc.format | application/pdf | en |
dc.format.extent | 339087 bytes | |
dc.format.mimetype | application/pdf | |
dc.identifier.doi | 10.1093/bioinformatics/bti730 | |
dc.identifier.uri | http://www.scopus.com/inward/record.url?eid=2-s2.0-28944447086&partnerID=MN8TOARS | |
dc.identifier.uri | http://scholars.lib.ntu.edu.tw/handle/123456789/314341 | |
dc.language | en | en |
dc.relation | Bioinformatics 21 (24): 4330-4337 | en |
dc.relation.ispartof | Bioinformatics | en_US |
dc.relation.journalissue | 24 | |
dc.relation.journalvolume | 21 | |
dc.relation.pages | 4330-4337 | |
dc.source | AH | |
dc.subject.classification | [SDGs]SDG3 | |
dc.subject.other | article; computer system; DNA hybridization; DNA probe; gene amplification; gene targeting; genetic algorithm; genetic selection; genus; intermethod comparison; microbiological examination; molecular probe; nonhuman; pathogenesis; plant virus; polymerase chain reaction; priority journal; process design; sensitivity and specificity; validation process; Algorithms; Base Sequence; Communicable Diseases; Computational Biology; DNA Primers; DNA Probes; Drug Design; Humans; Models, Genetic; Plant Viruses; Software Design; Thermodynamics; Virulence | |
dc.title | Integrated minimum-set primers and unique probe design algorithms for differential detection on symptom-related pathogens | |
dc.type | journal article | en |
dspace.entity.type | Publication |
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