pxlence - variant confirmation assays
Variant confirmation assays
Use the form below to quickly look up the assays covering your region of interest.
By chromosomal location (GRCh38) or gene identifier
By catalog number
pxlence' assays are designed to be highly specific. Our assessment of the impact of mismatches in primer annealing sites on PCR efficiency allows us to select assays resulting in the least degree of aspecific product generation
Fast and accurate
Our assays guarantee the shortest delivery time and high quality results. Our thorough in-silico validation pipeline combined with a high-quality oligo synthesis process ensures our customers a maximal PCR success rate
Every target
Our two assay catalogues cover almost 99% of the human exome, include sufficient intronic sequences to maximize Sanger-based exonic variant calling and are compatible with both high-quality DNA and degraded DNA samples (e.g FFPE)