Literature DB >> 24794070

Tools, resources and databases for SNPs and indels in sequences: a review.

Abhik Seal1, Arun Gupta2, M Mahalaxmi3, Riju Aykkal4, Tiratha Raj Singh5, Vadivel Arunachalam6.   

Abstract

Single Nucleotide Polymorphism (SNP) is a mutation where, a single base in the DNA differs from the usual base at that position. SNPs are the marker of choice in genetic analysis and also useful in locating genes associated with diseases. SNPs are important and frequently occurring point mutations in genomes and have many practical implications. In silico methods are easy to study the SNPs that are occurring in known genomes or sequences of a species of interest during the post genomic era. There are many on-line and stand alone tools to analyse the SNPs. We intend to guide the reader with the software details such as algorithmic background, file requirements, operating system specificity and species specificity, if any, for the tools of SNPs detection in plants and animals. We also list many databases and resources available today to describe SNPs in wide range of organisms.

Keywords:  SNP detection; SNPs; bioinformatics; data mining; databases; expressed sequence tags; indels; molecular markers; point mutations; sequences; single nucleotide polymorphisms; software

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Year:  2014        PMID: 24794070     DOI: 10.1504/IJBRA.2014.060762

Source DB:  PubMed          Journal:  Int J Bioinform Res Appl        ISSN: 1744-5485


  3 in total

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Journal:  J Assist Reprod Genet       Date:  2015-05-10       Impact factor: 3.412

Review 2.  Advances in the genome-wide association study of chronic hepatitis B susceptibility in Asian population.

Authors:  Bing Qiu; Wei Jiang; Mojtaba Olyaee; Kenji Shimura; Akihiro Miyakawa; Huijing Hu; Yongcui Zhu; Lixin Tang
Journal:  Eur J Med Res       Date:  2017-12-28       Impact factor: 2.175

3.  The Effects of WISP1 Polymorphisms on the Prognosis of Lung Cancer Patients with Platinum-Based Chemotherapy.

Authors:  Jia He; Zhan Wang; Ying Wang; Ting Zou; Xiang-Ping Li; Lei Cao; Juan Chen
Journal:  Pharmgenomics Pers Med       Date:  2021-09-18
  3 in total

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