Cell Ranger ATAC2.0, printed on 12/18/2024
The cellranger-atac count pipeline outputs a single position-sorted and indexed BAM file. These files are primarily provided for use with a BAM visualization tool such as the Integrated Genome Viewer (IGV).
| File | Records | Reference | Description |
| possorted_bam.bam | Reads | User-specified reference | Barcode-corrected reads aligned to the user-specified reference, sorted by reference position. |
| possorted_bam.bam.bai | Index | User-specified reference | Index file enabling random access to BAM by position |
The following assumes basic familiarity with the BAM format. More details on the SAM/BAM standard are available online.
Chromium cellular barcode and mapping information for each read is stored as TAG fields:
| Tag | Type | Description |
|---|---|---|
CB | Z | Chromium cellular barcode sequence that is error-corrected and confirmed against a list of known-good barcode sequences. |
CR | Z | Chromium cellular barcode sequence as reported by the sequencer. |
CY | Z | Chromium cellular barcode read quality. Phred scores as reported by sequencer. |
BC | Z | Sample index read. |
QT | Z | Sample index read quality. Phred scores as reported by sequencer. |
TR | Z | Adapter sequence trimmed off the end of the read. |
TQ | Z | Base quality for the trimmed adapater sequence. Phred scores as reported by sequencer. |
The cell barcode CB tag includes a gem group suffix "-1" that labels the GEMs
from a single channel.
AGAATGGTCTGCAT-1
cellranger-atac count only supports libraries generated
from a single GEM run and so the gem group suffix is always -1. It can either
be left in place and treated as part of a unique barcode identifier, or
explicitly parsed out to leave only the barcode sequence itself.