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Updated: Aug 14, 2026

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
Published on: June 23, 2012
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and
B Hoogendoorn1, N Norton, G Kirov
1Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom.
Abstract:
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjects poses a formidable problem for molecular genetic approaches to complex diseases. We have tested the possibility of using primer extension and denaturing high performance liquid chromatography to estimate allele frequencies of SNPs in pooled DNA samples. Our data show that this method should allow the accurate estimation of absolute allele frequencies in pooled samples of DNA and also of the difference in allele frequency between different pooled DNA samples. This technique therefore offers an efficient and cheap method for genotyping SNPs in large case-control and family-based association samples.

