The Chromium™ Single Cell Multiome ATAC + Gene Expression Solution produces Illumina® sequencer-ready libraries. Sequencing requirements for the two types of sequencing libraries produced are listed below.
Single Cell Multiome Gene Expression libraries
Compatible Sequencers
- Illumina® NovaSeq X Series
- Illumina® NovaSeq 6000
- Illumina® HiSeq 4000
- Illumina® HiSeq 2500 Rapid Run
- Illumina® NextSeq 500/550
- Illumina® NextSeq 1000/2000
- Illumina® MiSeq
Recommended Sequencing: Minimum 20,000 read pairs/cell*
Dual Indexed Sequencing Run: Single Cell Multiome Gene Expression libraries are dual-indexed. This means both i5 and i7 reads are used for demultiplexing. We do not recommend sequencing 10x Single Cell Multiome Gene Expression dual index libraries with a single-index configuration.
| Read | Read 1 | i7 Index | i5 Index | Read 2 |
|---|---|---|---|---|
| Purpose | Cell barcode & UMI | Sample Index | Sample Index | Insert |
| Length** | 28 | 10 | 10 | 90 |
*Adjust sequencing depth for the required performance or application. The Sequencing Saturation metric and curve in the Cell Ranger ARC run summary can be used to optimize sequencing depth for specific sample types.
**Shorter transcript reads may lead to reduced transcriptome alignment rates. Cell barcode, UMI and Sample index reads must not be shorter than indicated. Any read can be longer than recommended. Additional bases in Sample index reads must be trimmed using cellranger mkfastq or Illumina's bcl2fastq prior to further analysis. Additional bases in Cell barcode or UMI reads will automatically be ignored by Cell Ranger ARC.
Further information on sequencing specifications and expected data metrics can be found in the Sequencing Metrics & Base Composition of SC3' v3.1 Dual Index Libraries technical note.
Single Cell Multiome ATAC Libraries
Recommended Sequencing Depth: 25,000 read pairs per nucleus (50,000 individual reads. 25,000 from R1, 25,000 from R2)*
Dual-Indexed Sequencing Run: Single Cell Multiome ATAC libraries are dual-indexed. Please note, only the i7 index read is used for demultiplexing. The i5 index read is used to capture the 10x barcode information.
PhiX Spike-In Recommendations: 1%.
| Read | Read 1 | i7 Index | i5 Index | Read 2 |
|---|---|---|---|---|
| Purpose | Transposed DNA | Sample Index | 10x Barcode | Transposed DNA |
| Length | 50 ** | 8 | 24† | 49 ** |
* Adjust sequencing depth for the required performance or application. The Sequencing Saturation metric and curve in the Cell Ranger ARC run summary can be used to optimize sequencing depth for specific sample types.
** Sequence length can be adjusted based on sequencing kit used.
† Sequencers that do not support a 24bp i5 index read, require a custom sequencing recipe. See: Why do I need a custom recipe when sequencing Multiome ATAC libraries on the NextSeq?
Further information on sequencing specifications and expected data metrics can be found in the Sequencing Metrics & Base Composition of Single Cell Multiome ATAC Libraries technical note.
For any additional help or clarification, contact Support at Support@10xgenomics.com.