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PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens

BACKGROUND: Here we describe PathogenMIPer, a software program for designing molecular inversion probe (MIP) oligonucleotides for use in pathogen identification and detection. The software designs unique and specific oligonucleotide probes targeting microbial or other genomes. The tool tailors all p...

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Autores principales: Thiyagarajan, Sreedevi, Karhanek, Miloslav, Akhras, Michael, Davis, Ronald W, Pourmand, Nader
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1657037/
https://www.ncbi.nlm.nih.gov/pubmed/17105657
http://dx.doi.org/10.1186/1471-2105-7-500
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author Thiyagarajan, Sreedevi
Karhanek, Miloslav
Akhras, Michael
Davis, Ronald W
Pourmand, Nader
author_facet Thiyagarajan, Sreedevi
Karhanek, Miloslav
Akhras, Michael
Davis, Ronald W
Pourmand, Nader
author_sort Thiyagarajan, Sreedevi
collection PubMed
description BACKGROUND: Here we describe PathogenMIPer, a software program for designing molecular inversion probe (MIP) oligonucleotides for use in pathogen identification and detection. The software designs unique and specific oligonucleotide probes targeting microbial or other genomes. The tool tailors all probe sequence components (including target-specific sequences, barcode sequences, universal primers and restriction sites) and combines these components into ready-to-order probes for use in a MIP assay. The system can harness the genetic variability available in an entire genome in designing specific probes for the detection of multiple co-infections in a single tube using a MIP assay. RESULTS: PathogenMIPer can accept sequence data in FASTA file format, and other parameter inputs from the user through a graphical user interface. It can design MIPs not only for pathogens, but for any genome for use in parallel genomic analyses. The software was validated experimentally by applying it to the detection of human papilloma virus (HPV) as a model system, which is associated with various human malignancies including cervical and skin cancers. Initial tests of laboratory samples using the MIPs developed by the PathogenMIPer to recognize 24 different types of HPVs gave very promising results, detecting even a small viral load of single as well as multiple infections (Akhras et al, personal communication). CONCLUSION: PathogenMIPer is a software for designing molecular inversion probes for detection of multiple target DNAs in a sample using MIP assays. It enables broader use of MIP technology in the detection through genotyping of pathogens that are complex, difficult-to-amplify, or present in multiple subtypes in a sample.
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spelling pubmed-16570372006-11-22 PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens Thiyagarajan, Sreedevi Karhanek, Miloslav Akhras, Michael Davis, Ronald W Pourmand, Nader BMC Bioinformatics Software BACKGROUND: Here we describe PathogenMIPer, a software program for designing molecular inversion probe (MIP) oligonucleotides for use in pathogen identification and detection. The software designs unique and specific oligonucleotide probes targeting microbial or other genomes. The tool tailors all probe sequence components (including target-specific sequences, barcode sequences, universal primers and restriction sites) and combines these components into ready-to-order probes for use in a MIP assay. The system can harness the genetic variability available in an entire genome in designing specific probes for the detection of multiple co-infections in a single tube using a MIP assay. RESULTS: PathogenMIPer can accept sequence data in FASTA file format, and other parameter inputs from the user through a graphical user interface. It can design MIPs not only for pathogens, but for any genome for use in parallel genomic analyses. The software was validated experimentally by applying it to the detection of human papilloma virus (HPV) as a model system, which is associated with various human malignancies including cervical and skin cancers. Initial tests of laboratory samples using the MIPs developed by the PathogenMIPer to recognize 24 different types of HPVs gave very promising results, detecting even a small viral load of single as well as multiple infections (Akhras et al, personal communication). CONCLUSION: PathogenMIPer is a software for designing molecular inversion probes for detection of multiple target DNAs in a sample using MIP assays. It enables broader use of MIP technology in the detection through genotyping of pathogens that are complex, difficult-to-amplify, or present in multiple subtypes in a sample. BioMed Central 2006-11-14 /pmc/articles/PMC1657037/ /pubmed/17105657 http://dx.doi.org/10.1186/1471-2105-7-500 Text en Copyright © 2006 Thiyagarajan 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 Software
Thiyagarajan, Sreedevi
Karhanek, Miloslav
Akhras, Michael
Davis, Ronald W
Pourmand, Nader
PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title_full PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title_fullStr PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title_full_unstemmed PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title_short PathogenMIPer: a tool for the design of molecular inversion probes to detect multiple pathogens
title_sort pathogenmiper: a tool for the design of molecular inversion probes to detect multiple pathogens
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1657037/
https://www.ncbi.nlm.nih.gov/pubmed/17105657
http://dx.doi.org/10.1186/1471-2105-7-500
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