Cell Ranger2.1, printed on 12/24/2024
Though cellranger mkfastq is the preferred option for converting BCLs to Cell Ranger--compatible FASTQs, there are a few cases where you may need to use Illumina's bcl2fastq directly to generate FASTQs. This will be necessary if you do not wish to demultiplex an entire flow cell at once. You may also choose this method if bcl2fastq is more tightly integrated into your sequencing workflow.
Demultiplexing Chromium data with Illumina bcl2fastq requires the correct specification of the sample sheet and command-line options. This guide will walk you through what you'll need to do to generate Cell Ranger-compatible FASTQs.
You will need to create a sample sheet in order to get bcl2fastq to correctly embed the names of samples into output FASTQ files. There is a key difference to keep in mind when creating sample sheets for a Chromium run. Each Chromium sample index set is actually a blend of 4 different sequence oligos, and each oligo must be represented as a separate row in the sample sheet. This means that for every sample being demultiplexed from the flowcell, there should be 4 lines in the sample sheet.
The tool below will help you accurately generate data lines for your sample sheet. When you plan an experiment, you should know the name of the sample index set used for each sample, which comes from the reagent kit (such as "SI-P01-A2"). For each sample, enter its lane, sample name, and sample index set below, and then press 'Add'. When you're done, you can either copy and paste comma-separated output directly into a text editor to create a sample sheet CSV, or copy/paste tab-separated output into a spreadsheet such as Microsoft Excel:
If you are just running a single sample in a lane, then you can have a single line with the index blank, though bcl2fastq will include reads associated with any sample index.
Illumina bcl2fastq must be called with the correct --use-bases-mask argument and other arguments in order to properly demultiplex and output FASTQs for all the reads in a Chromium library.
In the examples below, ${FLOWCELL_DIR} is the directory that contains a flowcell's Data folder, ${OUTPUT_DIR} is the directory that you want to output FASTQs to, and
${SAMPLE_SHEET_PATH} is the path to the sample sheet CSV you created.
bcl2fastq Version 2.17 or higher
This is the most common case, for sequencers running RTA 1.18.54 and higher.
$ bcl2fastq --use-bases-mask=Y26,I8,Y98 \ --create-fastq-for-index-reads \ --minimum-trimmed-read-length=8 \ --mask-short-adapter-reads=8 \ --ignore-missing-positions \ --ignore-missing-controls \ --ignore-missing-filter \ --ignore-missing-bcls \ -r 6 -w 6 \ -R ${FLOWCELL_DIR} \ --output-dir=${OUTPUT_DIR} \ --interop-dir=${INTEROP_DIR} \ --sample-sheet=${SAMPLE_SHEET_PATH}
Version 1.8.4
$ configureBclToFastq.pl --use-bases-mask=Y26,I8,Y98 \ --fastq-cluster-count=20000000 \ --no-eamss \ --ignore-missing-bcl \ --ignore-missing-control \ --ignore-missing-stats \ --mismatches=1 \ --input-dir=${FLOWCELL_DIR}/Data/Intensities/BaseCalls \ --output-dir=${OUTPUT_DIR}
In both cases, if you want to limit bcl2fastq to a subset of lanes, you will need to supply values
to the --tiles argument.
If you add extra bases to a sample index read, you will need to account for this in the
--use-bases-mask argument. For example, if you ran a sample index read with 9 bases, you will need to
truncate the last base in order for Cell Ranger to run correctly.
You can exclude a single base by adding a single n character to
the read argument, or adding n* to exclude all bases after a certain position. See below:
Single Cell 3' v1 chemistry
| Read | Desired | Actual | Argument |
|---|---|---|---|
| i5 Index Read (I2) | 8 | 9 | I8n |
Single Cell 3' v2 chemistry
| Read | Desired | Actual | Argument |
|---|---|---|---|
| i7 Index Read (I1) | 8 | 9 | I8n |
For Single Cell 3' v1 samples, extra cycles on the i7 index read (cell-barcode) and R2 (UMI) reads will be ignored. By default, all of R1 (the RNA read) is used.
For Single Cell 3' v2 samples, extra cycles on the R1 (cell-barcode, UMI) read will be ignored. By default, all of R2 (the RNA read) is used.
After generating FASTQs, you should be able to follow the pipeline instructions, with one caveat. Instead of using
the --indices argument to cellranger to select samples, you will use the --sample argument. The
value of --sample should be the name of the sample, which should have been in the Sample_Name
column in your sample sheet. The value of --fastqs should be ${OUTPUT_DIR}/${PROJECT_NAME} where ${OUTPUT_DIR} is as defined above
and ${PROJECT_NAME} is the value in the Sample_Project column in the sample sheet.