» Articles » PMID: 16503968

SNP-RFLPing: Restriction Enzyme Mining for SNPs in Genomes

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2006 Mar 1
PMID 16503968
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The restriction fragment length polymorphism (RFLP) is a common laboratory method for the genotyping of single nucleotide polymorphisms (SNPs). Here, we describe a web-based software, named SNP-RFLPing, which provides the restriction enzyme for RFLP assays on a batch of SNPs and genes from the human, rat, and mouse genomes.

Results: Three user-friendly inputs are included: 1) NCBI dbSNP "rs" or "ss" IDs; 2) NCBI Entrez gene ID and HUGO gene name; 3) any formats of SNP-in-sequence, are allowed to perform the SNP-RFLPing assay. These inputs are auto-programmed to SNP-containing sequences and their complementary sequences for the selection of restriction enzymes. All SNPs with available RFLP restriction enzymes of each input genes are provided even if many SNPs exist. The SNP-RFLPing analysis provides the SNP contig position, heterozygosity, function, protein residue, and amino acid position for cSNPs, as well as commercial and non-commercial restriction enzymes.

Conclusion: This web-based software solves the input format problems in similar softwares and greatly simplifies the procedure for providing the RFLP enzyme. Mixed free forms of input data are friendly to users who perform the SNP-RFLPing assay. SNP-RFLPing offers a time-saving application for association studies in personalized medicine and is freely available at http://bio.kuas.edu.tw/snp-rflp/.

Citing Articles

Lack of Association Between BsmI and FokI Polymorphisms of the VDR Gene and Sporadic Colorectal Cancer in a Romanian Cohort-A Preliminary Study.

Petre-Mandache B, Burada E, Cucu M, Atasie D, Riza A, Streata I Curr Oncol. 2024; 31(10):6406-6418.

PMID: 39451780 PMC: 11505952. DOI: 10.3390/curroncol31100476.


AS-LAMP: A New and Alternative Method for Genotyping.

Gill P, Hadian Amree A Avicenna J Med Biotechnol. 2020; 12(1):2-8.

PMID: 32153732 PMC: 7035465.


Genomic Variants Among Threatened Corals.

Kitchen S, Ratan A, Bedoya-Reina O, Burhans R, Fogarty N, Miller W G3 (Bethesda). 2019; 9(5):1633-1646.

PMID: 30914426 PMC: 6505131. DOI: 10.1534/g3.119.400125.


REHUNT: a reliable and open source package for restriction enzyme hunting.

Cheng Y, Liaw J, Kuo C BMC Bioinformatics. 2018; 19(1):178.

PMID: 30092755 PMC: 6085610. DOI: 10.1186/s12859-018-2168-4.


Engineering altered protein-DNA recognition specificity.

Bogdanove A, Bohm A, Miller J, Morgan R, Stoddard B Nucleic Acids Res. 2018; 46(10):4845-4871.

PMID: 29718463 PMC: 6007267. DOI: 10.1093/nar/gky289.


References
1.
Vincze T, Posfai J, Roberts R . NEBcutter: A program to cleave DNA with restriction enzymes. Nucleic Acids Res. 2003; 31(13):3688-91. PMC: 168933. DOI: 10.1093/nar/gkg526. View

2.
Packer B, Yeager M, Staats B, Welch R, Crenshaw A, Kiley M . SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes. Nucleic Acids Res. 2003; 32(Database issue):D528-32. PMC: 308740. DOI: 10.1093/nar/gkh005. View

3.
Thiel T, Kota R, Grosse I, Stein N, Graner A . SNP2CAPS: a SNP and INDEL analysis tool for CAPS marker development. Nucleic Acids Res. 2004; 32(1):e5. PMC: 373308. DOI: 10.1093/nar/gnh006. View

4.
Bikandi J, San Millan R, Rementeria A, Garaizar J . In silico analysis of complete bacterial genomes: PCR, AFLP-PCR and endonuclease restriction. Bioinformatics. 2004; 20(5):798-9. DOI: 10.1093/bioinformatics/btg491. View

5.
Niu T, Hu Z . SNPicker: a graphical tool for primer picking in designing mutagenic endonuclease restriction assays. Bioinformatics. 2004; 20(17):3263-5. DOI: 10.1093/bioinformatics/bth360. View