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Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA
Author(s) -
P. Warnecke,
Clare Stirzaker,
J R Melki,
David Millar,
Christine Paul,
Susan J. Clark
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.21.4422
Subject(s) - biology , multiple displacement amplification , dna methylation , bisulfite sequencing , primer dimer , microbiology and biotechnology , dna , genomic dna , illumina methylation assay , genetics , polymerase chain reaction , methylation , methylated dna immunoprecipitation , dna sequencing , gene , dna extraction , multiplex polymerase chain reaction , gene expression
Methylation analysis of individual cytosines in genomic DNA can be determined quantitatively by bisulphite treatment and PCR amplification of the target DNA sequence, followed by restriction enzyme digestion or sequencing. Methylated and unmethylated molecules, however, have different sequences after bisulphite conversion. For some sequences this can result in bias during the PCR amplification leading to an inaccurate estimate of methylation. PCR bias is sequence dependent and often strand-specific. This study presents a simple method for detection and measurement of PCR bias for any set of primers, and investigates parameters for overcoming PCR bias.

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