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Svensson, Håkan
Publications (2 of 2) Show all publications
Lopes Pinto, F., Svensson, H. & Lindblad, P. (2007). Webtag: A new web tool providing tags/anchors for RT-PCR experiments with prokaryotes. BMC Biotechnology, 7, 73
Open this publication in new window or tab >>Webtag: A new web tool providing tags/anchors for RT-PCR experiments with prokaryotes
2007 (English)In: BMC Biotechnology, ISSN 1472-6750, E-ISSN 1472-6750, Vol. 7, p. 73-Article in journal (Refereed) Published
Abstract [en]

Background: Webtag is a tool providing oligonucleotide sequences (usually called tags or anchors) that are absent from a specified genome. These tags/anchors can be appended to gene specific primers for reverse transcriptase polymerase chain reaction experiments, circumventing genomic DNA contamination. Results: The use of a relational database, in conjunction with a series of scripts written in PHP and Perl, allows the user to rapidly obtain tags that are: 1) suitable for a specific organism, and 2) compatible with other oligonucleotides to be used in the experimental procedures. Conclusion: This new web tool allows scientists to easily and rapidly obtain suitable tags for RTPCR experiments, and is available at http://www.egs.uu.se/software/webtag/.

National Category
Biological Sciences
Identifiers
urn:nbn:se:uu:diva-13840 (URN)10.1186/1472-6750-7-73 (DOI)000251903100001 ()17961214 (PubMedID)
Available from: 2008-01-28 Created: 2008-01-28 Last updated: 2017-12-11Bibliographically approved
Lopes Pinto, F., Svensson, H. & Lindblad, P. (2006). Generation of non-genomic oligonucleotide tag sequences for RNA template-specific PCR. BMC Biotechnology, 6, 31
Open this publication in new window or tab >>Generation of non-genomic oligonucleotide tag sequences for RNA template-specific PCR
2006 (English)In: BMC Biotechnology, ISSN 1472-6750, E-ISSN 1472-6750, Vol. 6, p. 31-Article in journal (Refereed) Published
Abstract [en]

Background

In order to overcome genomic DNA contamination in transcriptional studies, reverse template-specific polymerase chain reaction, a modification of reverse transcriptase polymerase chain reaction, is used. The possibility of using tags whose sequences are not found in the genome further improves reverse specific polymerase chain reaction experiments. Given the absence of software available to produce genome suitable tags, a simple tool to fulfill such need was developed.

Results

The program was developed in Perl, with separate use of the basic local alignment search tool, making the tool platform independent (known to run on Windows XP and Linux). In order to test the performance of the generated tags, several molecular experiments were performed. The results show that Tagenerator is capable of generating tags with good priming properties, which will deliberately not result in PCR amplification of genomic DNA.

Conclusion

The program Tagenerator is capable of generating tag sequences that combine genome absence with good priming properties for RT-PCR based experiments, circumventing the effects of genomic DNA contamination in an RNA sample.

Keywords
Tagenerator, RT-PCR
National Category
Biochemistry and Molecular Biology Bioinformatics and Systems Biology
Identifiers
urn:nbn:se:uu:diva-81352 (URN)10.1186/1472-6750-6-31 (DOI)16820068 (PubMedID)
Available from: 2006-08-18 Created: 2006-08-18 Last updated: 2017-12-14Bibliographically approved
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