PCR designer for restriction analysis of various types of sequence mutation

Xiayi Ke, Andrew Collins, Shu Ye

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Summary: Restriction analysis is widely used to detect gene mutations such as insertions, deletions and single nucleotide polymorphisms (SNPs). Although such mutation sites sometimes present some natural restriction sites to differentiate the wild-type and mutant sequences, mismatches are often needed in order to create artificial restriction fragment length polymorphisms (RFLPs). In this report, a computer program is described that screens for suitable restriction enzymes, introducing mismatches where appropriate and when necessary, designs primers using the information of the selected restriction enzymes, their recognition sequence and locations as well as the information about the mismatches if any. The program, supported by a WWW web interface, is intended to be used online.
    Original languageEnglish
    Pages (from-to)1688-1689
    Number of pages1
    JournalBioinformatics
    Volume18
    Issue number12
    DOIs
    Publication statusPublished - 1 Dec 2002

    Keywords

    • genetics: Amidohydrolases
    • Base Pair Mismatch
    • Base Sequence
    • Biotinidase
    • Computer-Aided Design
    • chemistry: DNA Primers
    • chemistry: DNA Restriction Enzymes
    • Databases, Protein
    • Humans
    • methods: Information Storage and Retrieval
    • Internet
    • Molecular Sequence Data
    • genetics: Mutation
    • genetics: Point Mutation
    • methods: Polymerase Chain Reaction
    • methods: Restriction Mapping
    • methods: Sequence Analysis, DNA
    • Software

    Fingerprint

    Dive into the research topics of 'PCR designer for restriction analysis of various types of sequence mutation'. Together they form a unique fingerprint.

    Cite this