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MutScreener: primer design tool for PCR-direct sequencing
In searching for susceptibility genes, both positional cloning and candidate gene strategies have been helpful. Mutation screening is one of the many technologies that have been implemented in order to identify mutations or polymorphisms in candidate genes or genomic regions. Since human genome sequ...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538803/ https://www.ncbi.nlm.nih.gov/pubmed/16845093 http://dx.doi.org/10.1093/nar/gkl168 |
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author | Yao, Fengxia Zhang, Ruifang Zhu, Zanhua Xia, Kun Liu, Chunyu |
author_facet | Yao, Fengxia Zhang, Ruifang Zhu, Zanhua Xia, Kun Liu, Chunyu |
author_sort | Yao, Fengxia |
collection | PubMed |
description | In searching for susceptibility genes, both positional cloning and candidate gene strategies have been helpful. Mutation screening is one of the many technologies that have been implemented in order to identify mutations or polymorphisms in candidate genes or genomic regions. Since human genome sequence is available, PCR-direct sequencing is one of the major methods for mutation screening or resequencing. Unfortunately, assay design can be laborious if multiple genes or large regions need to be investigated. To solve this conundrum a web-based application, MutScreener, has been developed. MutScreener assists in the analysis of human gene structure and design of PCR/sequencing primer. This application supports batch assay design based on either existing public gene annotation or custom gene annotation. The optional universal tagged primers can support high throughput resequencing processes. MutScreener is available for public use at . |
format | Text |
id | pubmed-1538803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-15388032006-08-18 MutScreener: primer design tool for PCR-direct sequencing Yao, Fengxia Zhang, Ruifang Zhu, Zanhua Xia, Kun Liu, Chunyu Nucleic Acids Res Article In searching for susceptibility genes, both positional cloning and candidate gene strategies have been helpful. Mutation screening is one of the many technologies that have been implemented in order to identify mutations or polymorphisms in candidate genes or genomic regions. Since human genome sequence is available, PCR-direct sequencing is one of the major methods for mutation screening or resequencing. Unfortunately, assay design can be laborious if multiple genes or large regions need to be investigated. To solve this conundrum a web-based application, MutScreener, has been developed. MutScreener assists in the analysis of human gene structure and design of PCR/sequencing primer. This application supports batch assay design based on either existing public gene annotation or custom gene annotation. The optional universal tagged primers can support high throughput resequencing processes. MutScreener is available for public use at . Oxford University Press 2006-07-01 2006-07-14 /pmc/articles/PMC1538803/ /pubmed/16845093 http://dx.doi.org/10.1093/nar/gkl168 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Yao, Fengxia Zhang, Ruifang Zhu, Zanhua Xia, Kun Liu, Chunyu MutScreener: primer design tool for PCR-direct sequencing |
title | MutScreener: primer design tool for PCR-direct sequencing |
title_full | MutScreener: primer design tool for PCR-direct sequencing |
title_fullStr | MutScreener: primer design tool for PCR-direct sequencing |
title_full_unstemmed | MutScreener: primer design tool for PCR-direct sequencing |
title_short | MutScreener: primer design tool for PCR-direct sequencing |
title_sort | mutscreener: primer design tool for pcr-direct sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538803/ https://www.ncbi.nlm.nih.gov/pubmed/16845093 http://dx.doi.org/10.1093/nar/gkl168 |
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