DNA Next Generation Sequencing Facility
Pricing and Sample Requirements
Pricing is based on a cost-recovery model, and will vary depending on the experiment and data requirements. Please email Vanessa Schmid (email@example.com) for an estimate for your project.
Pricing includes primary and basic secondary computational analyses.
Rapid Runs are also available for sequencing lengths with 50-150 bp; ask for details.
Typical charges for samples in which the sequencing core makes the libraries are:
or # reads (M)
|Type||Read length (bp)||Samples|
|Exome (Human)||50X||2 μg||Paired-end||100||6||$900|
|Exome (Mouse)||50X||2 μg||Paired-end||100||6||$1200|
|mRNA, ss*||40M||5 μg||Single-end||50||4||$475|
|mRNA, ss||40M||5 μg||Paired-end||100||4||$725|
|Small RNA||25M||2 μg||Single-end||50||6||$450|
|Whole Transcriptome, ss||40M||2 μg||Single-end||50||4||$540|
|Whole Transcriptome, ss||40M||2 μg||Paired-end||100||4||$790|
|Whole Genome||40X||2 μg||Paired-end||100||0.25**||$8,590|
**Whole genome sequencing at 50X coverage requires sequencing of a single library in four lanes.