Analytical and bioanalytical chemistry, 1, 2015.
![Quantitative evaluation of bias in PCR amplification and next-generation sequencing derived from metabarcoding samples. [link]](https://bibbase.org/img/filetypes/link.svg "link")
Website doi abstract bibtex
Website doi abstract bibtex Unbiased identification of organisms by PCR reactions using universal primers followed by DNA sequencing assumes positive amplification. We used six universal loci spanning 48 plant species and quantified the bias at each step of the identification process from end point PCR to next-generation sequencing. End point amplification was significantly different for single loci and between species. Quantitative PCR revealed that Cq threshold for various loci, even within a single DNA extraction, showed 2,000-fold differences in DNA quantity after amplification. Next-generation sequencing (NGS) experiments in nine species showed significant biases towards species and specific loci using adaptor-specific primers. NGS sequencing bias may be predicted to some extent by the Cq values of qPCR amplification.
@article{
title = {Quantitative evaluation of bias in PCR amplification and next-generation sequencing derived from metabarcoding samples.},
type = {article},
year = {2015},
websites = {http://www.ncbi.nlm.nih.gov/pubmed/25577362},
month = {1},
day = {11},
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accessed = {2015-01-13},
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abstract = {Unbiased identification of organisms by PCR reactions using universal primers followed by DNA sequencing assumes positive amplification. We used six universal loci spanning 48 plant species and quantified the bias at each step of the identification process from end point PCR to next-generation sequencing. End point amplification was significantly different for single loci and between species. Quantitative PCR revealed that Cq threshold for various loci, even within a single DNA extraction, showed 2,000-fold differences in DNA quantity after amplification. Next-generation sequencing (NGS) experiments in nine species showed significant biases towards species and specific loci using adaptor-specific primers. NGS sequencing bias may be predicted to some extent by the Cq values of qPCR amplification.},
bibtype = {article},
author = {Pawluczyk, Marta and Weiss, Julia and Links, Matthew G and Egaña Aranguren, Mikel and Wilkinson, Mark D and Egea-Cortines, Marcos},
doi = {10.1007/s00216-014-8435-y},
journal = {Analytical and bioanalytical chemistry}
}Downloads: 0