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Related Concept Videos

DNA Isolation01:24

DNA Isolation

DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
Sanger Sequencing01:57

Sanger Sequencing

DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...

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Related Experiment Video

Updated: Jul 2, 2026

Methods to Increase the Sensitivity of High Resolution Melting Single Nucleotide Polymorphism Genotyping in Malaria
10:27

Methods to Increase the Sensitivity of High Resolution Melting Single Nucleotide Polymorphism Genotyping in Malaria

Published on: November 10, 2015

[A new method for SNP typing based on allele specific PCR].

Rui-Heng Wang1, Li-Min Liu, Jin-Ling Zhao

  • 1School of Forensic Medicine, China Medical University, Shenyang 110001, China. dalianwrh@sina.com

Fa Yi Xue Za Zhi
|August 20, 2008
PubMed
Summary

This study introduces a new SNP typing method using allele-specific PCR and capillary electrophoresis. The fragment length discrepant allele specific fluorescence labeled multi-PCR (FLDASFLM-PCR) method efficiently genotypes multiple SNPs simultaneously.

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Last Updated: Jul 2, 2026

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Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

Area of Science:

  • Molecular Biology
  • Genetics
  • Biotechnology

Context:

  • Single Nucleotide Polymorphisms (SNPs) are crucial genetic markers.
  • Accurate and efficient SNP typing is essential for genetic research and diagnostics.
  • Existing methods may have limitations in throughput or cost.

Purpose:

  • To develop a novel, efficient method for SNP typing.
  • To leverage allele-specific PCR and capillary electrophoresis for simultaneous multi-SNP analysis.
  • To establish a robust assay for genotyping multiple diallelic SNP loci.

Summary:

  • A new method, FLDASFLM-PCR, was developed using allele-specific primers and capillary electrophoresis.
  • Two forward primers of different lengths, with an artificial mismatch, were designed for each SNP.
  • Simultaneous amplification and analysis of 11 SNP loci were achieved, with results validated by direct sequencing.

Impact:

  • FLDASFLM-PCR offers a simple, rapid, and efficient approach for SNP typing.
  • This method facilitates high-throughput genotyping for genetic studies.
  • The technique provides accurate genotype determination for multiple SNPs in a single reaction.