Pricing is based on a cost-recovery model, and will vary depending on the experiment and data requirements. For an estimate, please email firstname.lastname@example.org.
Pricing includes primary and basic secondary computational analyses.
Rapid Runs are also available for sequencing lengths with 50-150 bp; please ask for details.
Typical charges for samples in which the sequencing core makes the libraries:
or # reads (M)
|Type||Read length (bp)||Price|
|Whole Transcriptome, ss**||35M||4||Single-end||50||$595|
|Whole Transcriptome, ss**||35M||4||Paired-end||100||$875|
*We guarantee 50X, usually get over 100X
***Whole genome sequencing at 40X coverage requires sequencing of a single library in four lanes.