Chromosome rearrangements, structural and copy number variation.

 For unfixed samples, the best way to do the exact analysis of structural variations is PacBio Revio long-read sequencing. 

For fixed samples, short reads are the best.

60x coverage short-read sequencing would be optimal for a batch size of 5 samples and would cost $660 per sample, including a library prep and sequencing. You would need to supply extracted DNA. We also offer DNA extraction. The pricing depends on the tissue type and fixation method. Please inquire.

 Additionally, we would charge $252 per sample for bioinformatic analysis of copy number variation. After that, additional custom bioinformatic analysis is charged at a rate of $105 per hour.

 The prices are of UCSD. Add 50% for the external prices.