Screening for mutations in human disease-causing genes in a molecular diagnostic environment demands simplicity with a view toallowing high throughput approaches. In order to advance these requirements, we have developed and applied a primer designprogram, termed BatchPD, to achieve the PCR amplification of coding exons of all known human Refseq genes. Primer design, insilico PCR checks and formatted primer information for subsequent web-based interrogation are queried from existing online tools.BatchPD acts as an intermediate to automate queries and results processing and provides exon-specific information that issummarised in a spreadsheet format.
CITATION STYLE
Lai, D., & Love, D. R. (2012). Automation of a primer design and evaluation pipeline for subsequent sequencing of the coding regions of all human Refseq genes. Bioinformation, 8(8), 365–368. https://doi.org/10.6026/97320630008365
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