10x Genomics
Chromium Single Cell Immune Profiling

Cell Ranger6.1, printed on 11/14/2024

Experimental Design for Immune Profiling

Table of Contents

• Sample Choice
• Recommended sequencing configuration for V(D)J
• How does performance vary as a function of sequencing depth?
• When might I need to sequence more?
• Should I use a different sequencing depth than the recommendation?
• How can I combine V(D)J data from one library sequenced across multiple lanes or flowcells?
• Can I use different read lengths?

Sample Choice

Human samples and mouse strains of types C57BL/6 and BALB/c have been tested. We provide primers and reference sequences that are known to work with these samples. If you use a different mouse strain, then it is possible that the primers and/or reference sequences will be insufficient. If you use another species, then you need to create your own primers and reference sequence. Note that defects in either could result in loss of clonotypes.

In general, spiking cell lines into your sample as a control may have unintended consequences. It may introduce high levels of background (particularly if the cell line cells are large or leaky), and it may confound the cell calling algorithm.

Recommended Sequencing Configuration for V(D)J

See the primary recommendation for V(D)J sequencing. This recommendation is repeated here. The following sections discuss the issues and choices available.

Cell refers to a recovered, targeted cell. A recovered cell is a cell captured in a GEM. A targeted cell may be a T or B cell, depending on which enrichment primers are used.

When you run CellRanger, the number of recovered targeted cells is estimated based on sequence data, whereas before sequencing is carried out, your estimate may be based on assays having higher variability and/or guesswork.

One reason we recommend 26 x 90 (or 26 x 91 for v1 chemistry) read pairs is that it facilitates efficient sequencing of multiple library types including V(D)J and GEX in a single sequencing run.

How does performance vary as a function of sequencing depth?

For most samples, the recommended sequencing depth will approach the limit of what you would obtain at high depth, even using longer (150 x 150) reads. However there are exceptions. Sequencing saturation in the following plots is computed as:

number of productive pairs obtained using 26 x 91 read pairs at given depth
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number of productive pairs obtained using 150 x 150 read pairs at high depth

Here high depth is ten-fold higher than the recommendation.

The plasma cell enriched sample is from a tumor, and in addition to having many plasma cells, may also have a significant fraction of dying cells.

When might I need to sequence more?

Some samples do not saturate at the recommended sequencing depth. The most common cause for this is extreme variation in expression levels between cells in a sample, so that the high expression cells soak up most of the sequencing, leaving little for the low expression cells. For example this could happen if:

• The sample contains many plasma B cells, which have roughly two orders of magnitude higher expression of IG genes than other B cells.
• The sample is from a tumor and contains many dying cells.

Samples for which overall expression levels are very low may also require greater sequencing depth to approach saturation.

Note that saturation may not be needed to achieve experimental goals. For example, obtaining data from many dying cells may or may not be useful.

Should I use a different sequencing depth than the recommendation?

Usually not. There are some exceptions, which depend on your sample type and the needs of your experiment:

• If your sample is precious and it is more important to get data from all cells than to save on sequencing cost, use higher depth.

• If recovery of low expression cells is critical to your experiment design, and your sample type is prone to high variation, use higher depth.

• If large savings on sequencing cost are more important than modest increases to yield, use lower depth.

How can I combine V(D)J data from one library sequenced across multiple lanes or flowcells?

If you have a library which was sequenced across multiple flowcells, you can pool the reads from both sequencing runs. Follow the steps in Specifying Input FASTQs to combine them in a single cellranger vdj run.

Can I use different read lengths?

We also support a 150 x 150 configuration:

This produces about the same number of read bases as the primary recommendation (26 x 91, 5000 read pairs per cell). The coverage response curves for these two configurations match closely.

Other read lengths may work but have not been tested. Coverage would need to be adjusted in the same fashion so that the number of read bases is about the same. Use of a second read that is significantly shorter than 91 bases may not work well.