• Skip to main content
  • Skip to primary sidebar

Nucleics

  • PeakTrace
    • About PeakTrace
    • PeakTrace Online
    • PeakTrace Online Pro
    • PeakTrace 6
    • PeakTrace:Box
    • PeakTrace RP
    • PeakTrace for Chromas
    • Buy PeakTrace
    • Why use PeakTrace?
    • Validation of PeakTrace
    • PeakTrace FAQ
    • PeakTrace In Depth
  • DNA Sequencing Products
    • PeakTrace Basecaller
    • PeakTrace:Box
    • PeakTrace RP
    • PeakTrace for Chromas
    • QualTrace
    • LongTrace
    • CounterTrace
    • dLUTE SEQ
    • UniSeq
    • ASIN
  • Support & Services
    • PeakTrace Online Pro Registration
    • QualTrace III Online
    • DNA Sequencing Troubleshooting Guide
    • PeakTrace RP Downloads
    • PeakTrace:Box Downloads
    • Trace Viewers
    • User Manuals
    • Help Guides
      • How to Install Auto PeakTrace 6
      • How to Upgrade to Auto PeakTrace 6
      • How to Update the PeakTrace License on Linux
      • How to Generate a cmDust File
      • Online Activation of Auto PeakTrace 6
      • Auto PeakTrace 6 Online Activation Guide
      • DNA Sequencing Protocols
        • DNA Sequencing Protocol Tips
        • Exonuclease I – Shrimp Alkaline Phosphatase Clean Up of PCR Products
        • Tris EDTA DNA Sequencing Resuspension Buffer
        • DNA Sequencing Reaction Clean-up using Phenol & Butanol
    • DNA Sequencing Service Reviews
    • Software Downloads
    • MSDS
    • Services
      • Genomics Sequencing
      • Bioinformatics
  • Forum
    • Register
    • Login
    • PeakTrace Basecaller Forum
    • PeakTrace:Box Forum
    • Auto PeakTrace RP Forum
    • QualTrace Forum
    • DNA Sequencing Forum
    • DNA Sequencing Software
    • PCR Forum
    • DNA Isolation Forum
    • LongTrace Forum
    • dLUTE SEQ Forum
  • About
    • Contact
    • News
    • Jobs
    • Nucleics Privacy Policy
Buy PeakTrace

Gene polymorphism

Home › Forums › DNA Sequencing Forum › Gene polymorphism

  • This topic has 1 reply, 2 voices, and was last updated 17 years, 11 months ago by FunctionalBio.
Viewing 1 reply thread
  • Author
    Posts
    • November 30, 2008 at 9:26 am #1344
      LLL
      Participant

      Can anyone help me w/my assignment? I’ve been given part of a gene (240bp; 301-541) with a polymorphism “y” at 405.I must design an assay and describe it in detail (controls, reagents, probes/primers, etc). Any info would be helpful. LL

    • December 4, 2008 at 9:27 am #1345
      FunctionalBio
      Participant

      Hi, i work for a sequencing service called Functional Biosciences, Inc. We offer SNP resequencing, so I know how to do this if you’re going to go with sequencing rather than probes etc.

      Just do a PCR reaction, making sure to run negative controls alongside your DNA samples. Do an exo sap clean up of the pcr reaction. Sequence from both directions using ABI big dye v 3.1, just use the pcr primers if the band on the gel looks clean. Theres a program called Mutation Surveyor that will analyze the traces at the polymorphic site. It can objectively designate each sample as a heterozygote or either type of homozygote. We have this software at our lab, its decent. Otherwise i think theres some free snp software here, [snp.wustl.edu]
      but i havent used any of it.

  • Author
    Posts
Viewing 1 reply thread
  • You must be logged in to reply to this topic.
Log In

Primary Sidebar

DNA Sequencing Help

We have added a guide on troubleshooting automated DNA sequencing problems.

DNA Sequencing Service Facilities Reviews

Please see our review of 325 DNA sequencing core facilities and commercial services for more information on selecting the right sequencing service for your needs.

QualTrace III Online

Try the free online version of the QualTrace DNA sequencing QC software and see how real time quality control tracking can improve your read lengths and lower sequencing failure rates.

Contact Details

email. information@nucleics.com
phone. +61 3 9016 9373
  • home
  • peaktrace
  • software & reagents
  • forum
  • tools
  • services
  • support
  • about

Nucleics

Sanger Seqencing Software

©Nucleics 1999 - 2026