GEM Generation and Barcoding
Melanie Königshoff, Melanie Königshoff, Nayra Cardenes, Robert Lafyatis, Heidi Monroe
Abstract
The Chromium Single Cell Gene Expression Solution upgrades short read sequencers to deliver a scalable microfluidic platform for 3’ digital gene expression by profiling 500-10,000 individual cells per sample.
A pool of ~3,500,000 10x Barcodes are sampled separately to index each cell’s transcriptome. It is done by partitioning thousands of cells (or nuclei) into nanoliter-scale Gel Beads-in-emulsion (GEMs), where all generated cDNA share a common 10x Barcode. Dual Indexed libraries are generated and sequenced from the cDNA and 10x Barcodes are used to associate individual reads back to the individual partitions.
This protocol outlines the process for generating Gel Beads-in-emulsion (GEMs) by combining barcoded Single Cell 3’ v3.1 Gel Beads, a Master Mix containing cells, and Partitioning Oil onto Chromium Next GEM Chip G. To achieve single cell resolution, cells are delivered at a limiting dilution, such that the majority (~90-99%) of generated GEMs contain no cell, while the remainder largely contain a single cell.
This protocol details the GEM Generation and Barcoding procedures.
Before start
Equilibrate to room temperature (RT) - Single Cell 3’ v3.1 Gel Beads (2000164), RT Reagent B (2000165) and Template Switch Oligo (3000228)* Place on ice – RT Enzyme C (20000085/2000102) and Cells suspension
- Prepare Master Mix - Prepare
On ice.
Attachments
Steps
GEM Generation and Barcoding
Prepare Master Mix On ice. Pipette mix 15× and centrifuge briefly.
Master Mix:
| A | B | C | D |
|---|---|---|---|
| Reagents | 1X (μl) | 4X+10% (μl) | 8X+10% (μl) |
| RT Reagent B | 18.8 | 82.7 | 165.4 |
| Template Switch Oligo | 2.4 | 10.6 | 21.1 |
| Reducing Agent B | 2 | 8.8 | 17.6 |
| RT Enzyme C | 8.7 | 38.3 | 76.6 |
| Total | 31.9 | 140.4 | 280.7 |
Add 31.9µL master mix into each tube of a PCR 8-tube strip On ice .
Assemble Chromium Next GEM Chip
Close the holder lid. Attach the gasket by holding the tongue (curved end, to the right) and hook the gasket on the left-hand tabs of the holder. Gently pull the gasket toward the right and hook it on the two right-hand tabs.
Remove the chip from the sealed bag, and use it within ≤ 24h 0m 0s.
Align notch on the chip (upper left corner) and the open holder with the gasket.
Slide the chip to the left until it is inserted under the guide on the holder. Depress the right hand side of the chip until the spring-loaded clip engages.
Keep the assembled unit open until all reagents have been loaded. Then close the chip holder.
Load Chromium NextGEM Chip G
Add 50% glycerol solution to each unused well (if processing <8 samples/chip)
70µLin each unused well in row labeled 150µLin each unused well in row labeled 245µLin each unused well in row labeled 3
Prepare Master Mix + Cell suspension:
Refer to the Cell Suspension Volume Calculator Table (refer to Chromium Next GEM Single Cell 3ʹ user Guide).
Add the appropriate volume of nuclease-free water to master mix. Pipette mix 5×. Add corresponding volume of single cell suspension to master mix. Total of 75µL in each tube.
Gently pipette mix the cell suspension before adding to the master mix.
Load Row Labeled 1
Gently pipette mix the Master Mix + Cell Suspension.
Using the same pipette tip, dispense 70µL master mix + cell suspension into the bottom center of each well in row labeled 1 without introducing bubbles.
Prepare Gel Beads
Snap the tube strip holder with the Gel Bead strip into a 10× Vortex Adapter. Vortex 0h 0m 30s.
Centrifuge the Gel Bead strip for ∼0h 0m 5s.
Confirm there are no bubbles at the bottom of the tubes and the liquid levels are even.
Place the Gel Bead strip back in the holder. Secure the holder lid.
Load Row Labeled 2
Puncture the foil seal of the Gel Bead tubes.
Slowly aspirate 50µL Gel Beads.
Dispense into the wells in row labeled 2 without introducing bubbles.
Wait 0h 0m 30s.
Load Row Labeled 3
Dispense 45µL partitioning oil into the wells in row labeled 3 from a reagent reservoir and close lid.
Run the Chromium Controller or X/iX
Press the eject button on the controller to eject the tray.
Place the assembled chip with the gasket in the tray, ensuring that the chip stays horizontal. Press the button to retract the tray.
Press the play button.
At completion of the run (∼0h 18m 0s), the Controller will chime. Immediately proceed to the next step.
Transfer GEMs
Place a tube strip On ice .
Press the eject button of the controller.
Discard the gasket. Open the chip holder. Fold the lid back until it clicks to expose the wells at 45 degrees
Visually compare the remaining volume in rows labeled 1-2. Abnormally high volume in one well relative to other wells may indicate a clog.
Slowly aspirate 100µL GEMs from the lowest points of the recovery wells in the top row labeled 3 without creating a seal between the tips and the bottom of the wells.
Over the course of ∼0h 0m 20s, dispense GEMs into the tube strip on ice with the pipette tips against the sidewalls of the tubes.
GEM-RT Incubation
Incubate in a thermal cycler with the following protocol:
| A | B | C |
|---|---|---|
| Lid Temperature | Reaction Volume | Run Time |
| 53°C | 125 µl | ~55 min |
| Step | Temperature | Time |
| 1 | 53°C | 45 min |
| 2 | 85°C | 5 min |
| 3 | 4°C | Hold |
Thermocycler protocol.
Store at 4°C for up to 72h 0m 0s or at -20°C for up to a week, or proceed to the next step.
