Feb 26, 2025
Evercode Single Index PCR
Forked from Evercode Single Index PCR
- Parse Biosciences1,
- Elisabeth Rebboah2
- 1Parse Biosciences;
- 2University of California, Irvine
External link: https://www.parsebiosciences.com/
Protocol Citation: Parse Biosciences, Elisabeth Rebboah 2025. Evercode Single Index PCR. protocols.io https://dx.doi.org/10.17504/protocols.io.bp2l6dj9rvqe/v1
Manuscript citation:
Rosenberg, A.B., Roco, C.M., Muscat, R.A., Kuchina, A., Sample, P., Yao, Z., Graybuck, L.T., Peeler, D.J., Mukherjee, S., Chen, W., Pun, S.H., Sellers, D.L., Tasic, B., and Seelig, Georg (2018). Single-cell profiling of the developing mouse brain and spinal cord with split-pool barcoding. Science, 360(6385), 176-182.
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: February 25, 2025
Last Modified: February 26, 2025
Protocol Integer ID: 123396
Keywords: single-cell, single-nucleus, snRNA-seq, scRNA-seq, Parse Bio, split-seq, index pcr procedure for parse biosciences evercode wt, evercode single index pcr, evercode single index pcr this protocol, parse biosciences evercode wt, sequence of the illumina barcode, index pcr procedure, unique barcodes across subpool, evercode, barcode in order, cdna library, illumina barcode, unique barcode, sequencing, single illumina index, barcode, sequencing run, wt mega v2 kit, experiment metadata, final cell id, subpool demultiplexing, pcr
Abstract
This protocol describes the single-index PCR procedure for Parse Biosciences Evercode WT and WT Mega v2 kits. Each subpool is barcoded with a single Illumina index on the 3' end of the cDNA library. This acts as the fourth "round" of cell barcoding and must be included in the final cell ID/barcode in order to ensure unique barcodes across subpools within an experiment. The numerical ID and sequence of the Illumina barcode used for each subpool are recorded in experiment metadata and used downstream for subpool demultiplexing after the sequencing run.
Troubleshooting
Appendix D2: Sublibrary Single Index PCR
If using unique dual indexes (UDIs) instead of sublibrary single index primers for indexing, see Section 3.5. Otherwise, replace the entirety of Section 3.5 with the following steps.
Multiple thermocyclers may be needed for this section depending on the amount of cDNA added to each sublibrary during the fragmentation reaction. Refer to step next page to determine how many thermocyclers are needed.
Using a new 1.5 mL tube, combine the Universal Index Primer and Index Primer Mix to make the Sublibrary Amplification Mix. Mix well by pipetting and store on ice.
| A | B | C | D | E | F | G | H | I | J | |
| # Sublibraries | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 16 | |
| Index PCR Mix | 27.5 | 55 | 82.5 | 110 | 137.5 | 165 | 192.5 | 220 | 440 | |
| Universal Index Primer | 2.2 | 4.4 | 6.6 | 8.8 | 11 | 13.2 | 15.4 | 17.6 | 35.2 | |
| Total | 29.7 | 59.4 | 89.1 | 118.8 | 148.5 | 178.2 | 207.9 | 237.6 | 465.2 |
Add 2 μL of different index primers to each sublibrary ensuring that no two sublibraries contain the same sublibrary index primer. Make sure to record which sublibrary contains which index primer.
Add 27 μL Sublibrary Amplification Mix to the 23 μL sublibrary from the previous step. Pipette up and down 10x with the pipette set to 27 μL to ensure proper mixing, followed by brief centrifugation (~2 sec).
Place the samples(s) into a thermocycler and run the program below. The number of cycles (X) should be adjusted based on the amount of cDNA added to the fragmentation reaction.
| Run Time | Lid Temperature | Sublibrary Volume | |
| ~30 min | 105C | 50 uL |
Sublibrary Index Amplification Overview
| Step | Time | Temperature | |
| 1 | 3 min | 95C | |
| 2 | 20 sec | 98C | |
| 3 | 20 sec | 67C | |
| 4 | 1 min, then go to step 2, repeat X-1 times (X cycles total) | 72C | |
| 5 | 5 min | 72C | |
| 6 | Hold | 4C |
Sublibrary Index Amplification
| A | B | C | D | E | F | G | |
| cDNA in Fragmentation (ng) | 10-24 | 25-49 | 50-99 | 100-299 | 300-999 | 1,000+ | |
| Total PCR cycles required (X) | 13 | 12 | 11 | 10 | 9 | 7 |
PCR Cycles based on cDNA in Fragmentation
Note: cDNA concentration was recorded in step 2.5.18, and 10 μL from each sublibrary should have been added into the fragmentation reaction (step 3.1.2).
Sublibraries can be stored at this point at 4°C overnight. If you wish to continue, proceed directly to Section 3.6: Post-Amplification Double-Sided Size Selection.
[STOPPING POINT]