Prepaid DNA sequencing vouchers
Benefits of using vouchers
- Cost savings - buying a full book of vouchers
discounts your individual read by as much as 15%
- Ease of use:
- No time-consuming attachment of labels
- No complicated barcode allocation or tedious re-labelling
required
- Advanced payment to assist year-end
budgeting
- Only one PO number and one invoice per
order
- Faster ordering process - no payment at
checkout
DNA sequencing voucher pricing
|
Cat No
|
Description
|
Qty
|
Price
|
|
GSL1501
|
50 prepaid single read vouchers
|
50
|
£332.50
|
|
GSL1601
|
100 prepaid single read vouchers
|
100
|
£640.00
|
|
GSL1596
|
5 x 96 well plate prepaid read
vouchers
|
5 x 96
|
£2660.00
|
Prices vary for different institutions, your institution may
qualify for a discount. Please contact us to
check what pricing structure you are eligible for.
How to use the vouchers
- Register on the Source BioScience
LifeSciences website. It only takes a couple of minutes
- Complete the order online noting payment by vouchers in
the Sequencing Vouchers section
- Place your samples in a padded envelope so that they are well
protected
- Download a FREEPOST label, or drop your samples off at your
nearest collection box. We have labels for Nottingham, Cambridge, Oxford, UCL
and Dublin
PLEASE REMEMBER TO INCLUDE YOUR
VOUCHERS WITH YOUR SAMPLES.
Why choose Source BioScience LifeSciences
- Quality: The reads we generate have been
benchmarked against leading industry providers. We strive to get
the best data possible from your DNA and can provide up to 1,400
base reads
- Turnaround time: With our new Overnight
Service combined with SpeedREAD™, we can provide the worlds fastest
turnaround time for your results
- Ease of ordering: Our online ordering
system means no mistakes with sample labelling or sample sheet
creation, data is automatically tracked through our laboratory
information system
- Reliability: We do not rely on a single piece
of hardware so we always have machine availability even during
times of machine maintenance
- Experience: We have completed over 30 million
bases of genomic finished sequence but we are happy to work on any
sized project