Submit Samples for Illumina Sequencing
Follow these steps to submit all new requests
- Have a consultation for all new projects
- Sign up for a LockBox Account
- Prepare your index list
- NOTE: You will download our template to upload into LockBox - no other formats accepted
- Submit your request(s) - use the references here as a guide
- Drop your samples off and log them - drop-off details here
How to Submit your Samples or Pool(s)
Submit Samples in the Following Formats:
- >16 Samples must be arrayed in a 96-well plate in full columns (A-H) without spaces
- Label the side of the plate with your name, submission ID, and date
- 4-16 samples/pools
- PCR strip tubes with caps -labeled with # on sample import template
- 1-4 samples/pools
- 1.5 mL tubes or strip tubes - clearly labeled including the # on the sample import template
Do not submit samples in PCR tubes (0.2 mL) or 0.5 mL tubes
*NOTE: Samples received in other formats will not be accepted and have to be rearrayed by the researcher. The Core is not responsible for any delays.
Do not submit samples in PCR tubes (0.2 mL) or 0.5 mL tubes
Turnaround Times
Full Flow Cells:
- Most run within 2 weeks after qPCR
- They will run within 2 weeks without qPCR
- Email us if you'd like a better estimate.
Single Lanes:
- Take longer to fill, but we expect the most popular options to run within 2-3 weeks.
- If a quick turnaround is your main concern, we can suggest other options, email us.
Volumes and Concentrations
| Submission Volume and Concentration | ||
|---|---|---|
| Instrument and Run Type | *[nM] of Pool | *Volume per Lane/Flow Cell |
MiSeq or NextSeq 500 (any type) | 4 nM | 20 |
NextSeq 1000 (any type) | 4 nM | 40 |
NovaSeq X Plus 1.5B/5B/10B (any length) Per Lane (1.5B- 2 Lanes, 5B/10B- 8 Lanes per Flow Cell) | 4 nM | 40 |
NovaSeq X Plus 25B (any length) Per Lane (8 Lanes per Flow Cell) | 4 nM | 60 |
*lower library concentrations will be run at risk *If you need to submit samples <2 nM you should contact the sequencing team for additional guidance. | ||
- Submit your sequencing pool at the concentration and volume listed for your instrument and run type.
- Note you should multiply volume by the number of lanes or flow cells you plan to sequence.
- The core is not responsible for any delays if samples do not meet these requirements.