 |
|
|
You could potentially use resequencing arrays to tile for individual, widely spaced SNPs, but we don't recommend this strategy because it is not the most efficient use of the resequencing array. With resequencing arrays, you lose 24 bases or 192 features for each non-contiguous fragment. An alternative approach would be to design a custom SNP array containing only individual SNPs chosen by customers from public databases or the Perlegen database. This approach would maximize the number of SNPs you could assay on a given
array. Please keep in mind that assay strategies for custom SNP arrays can be complex and would be the responsibility of the customer. The design fees would also be higher for a custom SNP array than the current CustomSeq design fees.
|