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UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level

BACKGROUND: Nucleic acid hybridization is an extensively adopted principle in biomedical research, in which the performance of any hybridization-based method depends on the specificity of probes to their targets. To determine the optimal probe(s) for detecting target(s) from a sample cocktail, we de...

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Autores principales: Chen, Shu-Hwa, Lo, Chen-Zen, Su, Sheng-Yao, Kuo, Bao-Han, Hsiung, Chao A, Lin, Chung-Yen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005932/
https://www.ncbi.nlm.nih.gov/pubmed/21143815
http://dx.doi.org/10.1186/1471-2164-11-S4-S6
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author Chen, Shu-Hwa
Lo, Chen-Zen
Su, Sheng-Yao
Kuo, Bao-Han
Hsiung, Chao A
Lin, Chung-Yen
author_facet Chen, Shu-Hwa
Lo, Chen-Zen
Su, Sheng-Yao
Kuo, Bao-Han
Hsiung, Chao A
Lin, Chung-Yen
author_sort Chen, Shu-Hwa
collection PubMed
description BACKGROUND: Nucleic acid hybridization is an extensively adopted principle in biomedical research, in which the performance of any hybridization-based method depends on the specificity of probes to their targets. To determine the optimal probe(s) for detecting target(s) from a sample cocktail, we developed a novel algorithm, which has been implemented into a web platform for probe designing. This probe design workflow is now upgraded to satisfy experiments that require a probe designing tool to take the increasing volume of sequence datasets. RESULTS: Algorithms and probe parameters applied in UPS 2.0 include GC content, the secondary structure, melting temperature (Tm), the stability of the probe-target duplex estimated by the thermodynamic model, sequence complexity, similarity of probes to non-target sequences, and other empirical parameters used in the laboratory. Several probe background options,Unique probe within a group,Unique probe in a specific Unigene set,Unique probe based onthe pangenomic level, and Unique Probe in the user-defined genome/transcriptome, are available to meet the scenarios that the experiments will be conducted. Parameters, such as salt concentration and the lower-bound Tm of probes, are available for users to optimize their probe design query. Output files are available for download on the result page. Probes designed by the UPS algorithm are suitable for generating microarrays, and the performance of UPS-designed probes has been validated by experiments. CONCLUSIONS: The UPS 2.0 evaluates probe-to-target hybridization under a user-defined condition to ensure high-performance hybridization with minimal chance of non-specific binding at the pangenomic and genomic levels. The UPS algorithm mimics the target/non-target mixture in an experiment and is very useful in developing diagnostic kits and microarrays. The UPS 2.0 website has had more than 1,300 visits and 360,000 sequences performed the probe designing task in the last 30 months. It is freely accessible at http://array.iis.sinica.edu.tw/ups/. Screen cast: http://array.iis.sinica.edu.tw/ups/demo/demo.htm
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spelling pubmed-30059322010-12-22 UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level Chen, Shu-Hwa Lo, Chen-Zen Su, Sheng-Yao Kuo, Bao-Han Hsiung, Chao A Lin, Chung-Yen BMC Genomics Proceedings BACKGROUND: Nucleic acid hybridization is an extensively adopted principle in biomedical research, in which the performance of any hybridization-based method depends on the specificity of probes to their targets. To determine the optimal probe(s) for detecting target(s) from a sample cocktail, we developed a novel algorithm, which has been implemented into a web platform for probe designing. This probe design workflow is now upgraded to satisfy experiments that require a probe designing tool to take the increasing volume of sequence datasets. RESULTS: Algorithms and probe parameters applied in UPS 2.0 include GC content, the secondary structure, melting temperature (Tm), the stability of the probe-target duplex estimated by the thermodynamic model, sequence complexity, similarity of probes to non-target sequences, and other empirical parameters used in the laboratory. Several probe background options,Unique probe within a group,Unique probe in a specific Unigene set,Unique probe based onthe pangenomic level, and Unique Probe in the user-defined genome/transcriptome, are available to meet the scenarios that the experiments will be conducted. Parameters, such as salt concentration and the lower-bound Tm of probes, are available for users to optimize their probe design query. Output files are available for download on the result page. Probes designed by the UPS algorithm are suitable for generating microarrays, and the performance of UPS-designed probes has been validated by experiments. CONCLUSIONS: The UPS 2.0 evaluates probe-to-target hybridization under a user-defined condition to ensure high-performance hybridization with minimal chance of non-specific binding at the pangenomic and genomic levels. The UPS algorithm mimics the target/non-target mixture in an experiment and is very useful in developing diagnostic kits and microarrays. The UPS 2.0 website has had more than 1,300 visits and 360,000 sequences performed the probe designing task in the last 30 months. It is freely accessible at http://array.iis.sinica.edu.tw/ups/. Screen cast: http://array.iis.sinica.edu.tw/ups/demo/demo.htm BioMed Central 2010-12-02 /pmc/articles/PMC3005932/ /pubmed/21143815 http://dx.doi.org/10.1186/1471-2164-11-S4-S6 Text en Copyright © 2010 Chen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Chen, Shu-Hwa
Lo, Chen-Zen
Su, Sheng-Yao
Kuo, Bao-Han
Hsiung, Chao A
Lin, Chung-Yen
UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title_full UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title_fullStr UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title_full_unstemmed UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title_short UPS 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
title_sort ups 2.0: unique probe selector for probe design and oligonucleotide microarrays at the pangenomic/ genomic level
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005932/
https://www.ncbi.nlm.nih.gov/pubmed/21143815
http://dx.doi.org/10.1186/1471-2164-11-S4-S6
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