10x Genomics Support/Loupe Browser/Analysis/

Multiome Data Concepts

Exploring Multiome data shares similarities with analyzing Gene Expression or ATAC data. Here are key considerations for analyzing Multiome ATAC + Gene Expression data.

  • Both ATAC and Gene Expression data are available for the same cells. This means that many types of features are available for the same cell, including UMI counts per cell, cut sites per cell, transcription factor motif z-scores, and aggregate features (see below).

  • A pair of t-SNE and UMAP projections are computed from Gene Expression and ATAC data, respectively.

  • Peaks are genomic regions where there were significant upticks in fragment cut sites, which indicate regions of open chromatin. They are named by their location (e.g., "chr1:10244-10510").

  • Unlike genes, peaks are likely to vary between different datasets or even the same dataset sequenced at different depths.

  • Typically, there are more distinct peaks than there are genes.

  • The dynamic range of gene expression per cell is usually much wider than the dynamic range of cut sites per peak per cell.

  • A significant addition to a Multiome ATAC + Gene Expression dataset is the introduction of Feature Linkages. These represent correlations between gene expression and patterns of open chromatin across all cells in the dataset. Linked features can be gene-to-peak or peak-to-peak, and for linkage, features must be within a megabase of each other.

  • In addition to genes and peaks, there are several aggregate feature types that can also be used to differentiate cells:

    • Nearby gene sums: the sums of peak cut sites per cell (within peaks) that are close to any transcript of that gene. This is computed in all datasets with ATAC data, including Single Cell ATAC. The direct readout of Gene Expression data available in Single Cell Multiome ATAC + Gene Expression datasets may be more useful, but this is available for comparison.
    • Promoter sums: the sums of cut sites per cell (within peaks) that are close to one of the transcription start sites for that gene. These features are named "(Gene) Sum". Not all peaks are associated with a gene.
    • Transcription factor motifs: the sums of cut sites per cell that fall within peaks associated with a motif by the Cell Ranger ARC pipeline. Motif features are named after the motifs themselves (e.g., "SPI1"). A peak is usually associated with multiple motifs.
  • A Single Cell Multiome ATAC + Gene Expression dataset takes up several times as much disk space (per cell) than a Single Cell Gene Expression dataset, and a small amount more than Single Cell ATAC datasets.

  • To see fragment locations per cluster in high resolution, you need access to the atac_fragments.tsv.gz file for that run, generated by the Cell Ranger ARC pipeline. These files are typically several times larger than the .cloupe file, which is why they are not bundled. You can either specify the location of this file on a locally mounted file system, or the web via a URL.