Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays

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Abstract

Background: The recommended genomic DNA input requirements for whole genome single nucleotide polymorphism microarrays can limit the scope of molecular epidemiological studies. We performed a large-scale evaluation of whole genome amplified DNA as input into high-density, whole-genome Illumina® Infinium® SNP microarray. Results: Overall, 6622 DNA samples from 5970 individuals were obtained from three distinct biospecimen sources and genotyped using gDNA and/or wgaDNA inputs. When genotypes from the same individual were compared with standard, native gDNA input amount, we observed 99.94% mean concordance with wgaDNA input. Conclusions: Our results demonstrate that carefully conducted studies with wgaDNA inputs can yield high-quality genotyping results. These findings should enable investigators to consider expansion of ongoing studies using high-density SNP microarrays, currently challenged by small amounts of available DNA.

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Dagnall, C. L., Morton, L. M., Hicks, B. D., Li, S., Zhou, W., Karlins, E., … Chanock, S. J. (2018). Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays. BMC Genomics, 19(1). https://doi.org/10.1186/s12864-018-4572-6

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