Abstract
PCR amplification of limited amounts of DNA template carries an increased risk of product redundancy and contamination. We use molecular barcoding to label each genomic DNA template with an individual sequence tag prior to PCR amplification. In addition, we include molecular 'batch-stamps' that effectively label each genomic template with a sample ID and analysis date. This highly sensitive method identifies redundant and contaminant sequences and serves as a reliable method for positive identification of desired sequences; we can therefore capture accurately the genomic template diversity in the sample analyzed. Although our application described here involves the use of hairpin-bisulfite PCR for amplification of double-stranded DNA, the method can readily be adapted to single-strand PCR. Useful applications will include analyses of limited template DNA for biomedical, ancient DNA and forensic purposes.
MeSH Terms
Base Sequence
Fragile X Mental Retardation Protein
Genome, Human
Humans
Male
Molecular Sequence Data
Nerve Tissue Proteins/genetics
Polymerase Chain Reaction/methods
Promoter Regions, Genetic
RNA-Binding Proteins/genetics
Sequence Analysis, DNA/methods
Sulfites/chemistry
Templates, Genetic
Chemicals
FMR1 protein, human
Nerve Tissue Proteins
RNA-Binding Proteins
Sulfites
Fragile X Mental Retardation Protein
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Miner Brooks E
Department of Biology, University of Washington, Seattle, WA 98195, USA. miner@u.washington.edu
Stöger Reinhard J
Burden Alice F
Laird Charles D
Hansen R Scott
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