Pricing & Sample Submission

Pricing

Pricing is based on a cost-recovery model, and will vary depending on the experiment and data requirements. For an estimate, please email vanessa.schmid@utsouthwestern.edu.

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:

ProcedureCoverage (X)
or # reads (M)
Samples
/lane
TypeRead length (bp)Price
ChIP 25M 6 Single-end 50 $425
Exome (Human) 80X* 5 Paired-end 100 $900
Exome (Mouse) 80X* 5 Paired-end 100 $1,200
mRNA, ss** 25M 6 Single-end 50 $425
mRNA, ss** 35M 4 Paired-end 100 $800
Small RNA 25M 6 Single-end 50 $525
Whole Transcriptome, ss** 35M 4 Single-end 50 $595
Whole Transcriptome, ss** 35M 4 Paired-end 100 $875
Whole Genome 40X 0.25*** Paired-end 100 $7,500

*We guarantee 50X, usually get over 100X

**Strand-specific.

***Whole genome sequencing at 40X coverage requires sequencing of a single library in four lanes.