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SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping
BACKGROUND: PCR-restriction fragment length polymorphism (RFLP) assay is a cost-effective method for SNP genotyping and mutation detection, but the manual mining for restriction enzyme sites is challenging and cumbersome. Three years after we constructed SNP-RFLPing, a freely accessible database and...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858040/ https://www.ncbi.nlm.nih.gov/pubmed/20377871 http://dx.doi.org/10.1186/1471-2105-11-173 |
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author | Chang, Hsueh-Wei Cheng, Yu-Huei Chuang, Li-Yeh Yang, Cheng-Hong |
author_facet | Chang, Hsueh-Wei Cheng, Yu-Huei Chuang, Li-Yeh Yang, Cheng-Hong |
author_sort | Chang, Hsueh-Wei |
collection | PubMed |
description | BACKGROUND: PCR-restriction fragment length polymorphism (RFLP) assay is a cost-effective method for SNP genotyping and mutation detection, but the manual mining for restriction enzyme sites is challenging and cumbersome. Three years after we constructed SNP-RFLPing, a freely accessible database and analysis tool for restriction enzyme mining of SNPs, significant improvements over the 2006 version have been made and incorporated into the latest version, SNP-RFLPing 2. RESULTS: The primary aim of SNP-RFLPing 2 is to provide comprehensive PCR-RFLP information with multiple functionality about SNPs, such as SNP retrieval to multiple species, different polymorphism types (bi-allelic, tri-allelic, tetra-allelic or indels), gene-centric searching, HapMap tagSNPs, gene ontology-based searching, miRNAs, and SNP500Cancer. The RFLP restriction enzymes and the corresponding PCR primers for the natural and mutagenic types of each SNP are simultaneously analyzed. All the RFLP restriction enzyme prices are also provided to aid selection. Furthermore, the previously encountered updating problems for most SNP related databases are resolved by an on-line retrieval system. CONCLUSIONS: The user interfaces for functional SNP analyses have been substantially improved and integrated. SNP-RFLPing 2 offers a new and user-friendly interface for RFLP genotyping that can be used in association studies and is freely available at http://bio.kuas.edu.tw/snp-rflping2. |
format | Text |
id | pubmed-2858040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28580402010-04-22 SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping Chang, Hsueh-Wei Cheng, Yu-Huei Chuang, Li-Yeh Yang, Cheng-Hong BMC Bioinformatics Software BACKGROUND: PCR-restriction fragment length polymorphism (RFLP) assay is a cost-effective method for SNP genotyping and mutation detection, but the manual mining for restriction enzyme sites is challenging and cumbersome. Three years after we constructed SNP-RFLPing, a freely accessible database and analysis tool for restriction enzyme mining of SNPs, significant improvements over the 2006 version have been made and incorporated into the latest version, SNP-RFLPing 2. RESULTS: The primary aim of SNP-RFLPing 2 is to provide comprehensive PCR-RFLP information with multiple functionality about SNPs, such as SNP retrieval to multiple species, different polymorphism types (bi-allelic, tri-allelic, tetra-allelic or indels), gene-centric searching, HapMap tagSNPs, gene ontology-based searching, miRNAs, and SNP500Cancer. The RFLP restriction enzymes and the corresponding PCR primers for the natural and mutagenic types of each SNP are simultaneously analyzed. All the RFLP restriction enzyme prices are also provided to aid selection. Furthermore, the previously encountered updating problems for most SNP related databases are resolved by an on-line retrieval system. CONCLUSIONS: The user interfaces for functional SNP analyses have been substantially improved and integrated. SNP-RFLPing 2 offers a new and user-friendly interface for RFLP genotyping that can be used in association studies and is freely available at http://bio.kuas.edu.tw/snp-rflping2. BioMed Central 2010-04-08 /pmc/articles/PMC2858040/ /pubmed/20377871 http://dx.doi.org/10.1186/1471-2105-11-173 Text en Copyright ©2010 Chang 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 Chang, Hsueh-Wei Cheng, Yu-Huei Chuang, Li-Yeh Yang, Cheng-Hong SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title | SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title_full | SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title_fullStr | SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title_full_unstemmed | SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title_short | SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping |
title_sort | snp-rflping 2: an updated and integrated pcr-rflp tool for snp genotyping |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858040/ https://www.ncbi.nlm.nih.gov/pubmed/20377871 http://dx.doi.org/10.1186/1471-2105-11-173 |
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