10x Genomics
Chromium Single Cell ATAC

Cell Ranger ATAC1.0, printed on 12/18/2024

Run Analysis

The count pipeline outputs several CSV files which contain automated secondary analysis results. A subset of these results are used to render the Cell Clustering view in the run summary.

Dimensionality Reduction

Before clustering the cells, Latent Semantic Analysis (LSA) is run on the normalized filtered peak-barcode matrix to reduce the number of feature (peak) dimensions. This produces a projection of each cell onto the first N components (default N=15). One may alternatively choose Principal Component Analysis (PCA) or Probabilistic Latent Semantic Analysis (PLSA) to perform dimensionality reduction in the pipeline. All of these methods provide the following basic CSV output files.

$ cd /home/jdoe/runs/sample345/outs
$ head -2 analysis/lsa/15_components/projection.csv
Barcode,PC-1,PC-2,PC-3,PC-4,PC-5,PC-6,PC-7,PC-8,PC-9,PC-10,PC-11,PC-12,PC-13,PC-14,PC-15
AAATGAGCAATCAGGG-1,-2.0256188855237585,-20.464971914743963,2.4066208658862194,-0.9789882112497361,-0.09345960806751374,-8.483300343102174,-5.672765504454421,18.312955842984056,5.6927438340737195,-3.0378744705134992,0.3959335790734238,-4.93326991505897,9.485264727952154,0.2107363858043646,0.948135821430962

This also produces a components matrix which indicates how much each peak contributed to each component.

$ head -2 analysis/lsa/15_components/components.csv
PC,chr1:9695143-9697582,chr1:9698212-9701041,...
1,-0.5482991923678618,-0.6374211593177428,...

This also produces the proportion of total variance explained by each component. When choosing the number of components that are significant, it is useful to look at the plot of variance explained as a function of component rank - when the numbers start to flatten out, subsequent components are unlikely to represent meaningful variation in the data.

$ head -5 analysis/lsa/15_components/variance.csv
PC,Proportion.Variance.Explained
1,0.8452609977911579
2,0.032765042936590785
3,0.026127180307558735
4,0.01667142686188944

We also compute the normalized dispersion of each peak, after binning peaks by their mean expression across the dataset. This provides a useful measure of variability of each peak.

$ head -5 analysis/lsa/15_components/dispersion.csv
Feature,Normalized.Dispersion
chr1:9695143-9697582,0.02029960904777695
chr1:9698212-9701041,0.10379770925583033
chr1:9825253-9827762,-1.0
chr1:9829746-9830116,25.528012093307737

Visualization

After running PCA, t-distributed Stochastic Neighbor Embedding (t-SNE) is run to visualize cells in a 2-D space.

$ head -5 analysis/tsne/2_components/projection.csv
Barcode,TSNE-1,TSNE-2
AAATGAGCAATCAGGG-1,1.552159628302055,4.434829693735686
AACAAAGCACCTATTT-1,3.2188609791527667,0.03569781940043248
AACCTTTCAATGATGA-1,-3.8319704788291475,-1.092848944953291
AACTTGGCATGGCCGT-1,-4.226692514189564,0.3351938808086092

Clustering

Clustering is then run to group cells together that have similar accessibility profiles, based on their projection into lower dimensional space. Graph-based clustering (under graphclust) is run once as it does not require prespecification of the number of clusters. For PCA, K-means (under kmeans) is run for many values of K=2,...,N where K corresponds to the number of clusters. For LSA or PLSA, K-medoids (under kmedoids) is run over the same range of K. By default N=10. The corresponding results for each K is separated into its own directory.

$ ls analysis/clustering
graphclust            kmedoids_2_clusters  kmedoids_4_clusters
kmedoids_6_clusters   kmedoids_8_clusters  kmedoids_10_clusters
kmedoids_3_clusters   kmedoids_5_clusters  kmedoids_7_clusters
kmedoids_9_clusters

For each clustering, cellranger-atac produces cluster assignments for each cell.

$ head -5 analysis/clustering/kmedoids_3_clusters/clusters.csv
Barcode,Cluster
AAATGAGCAATCAGGG-1,2
AACAAAGCACCTATTT-1,1
AACCTTTCAATGATGA-1,3
AACTTGGCATGGCCGT-1,3

Differential Analysis

Prior to differential analysis, cellranger-atac produces a transcription factor-barcode matrix of counts as described in Matrices. cellranger-atac also produces a table indicating which transcription factor motifs are differentially active in each cluster relative to all other clusters. For each transcription factor motif we compute three values per cluster:

• The mean cut site counts per cell pooled in peaks associated with this transcription factor motif in cluster i.
• The log2 fold-change of this transcription factor motif's activity in cluster i relative to other clusters.
• The p-value denoting significance of this transcription factor motif's activity in cluster i relative to other clusters, adjusted to account for the number of hypotheses (i.e. transcription factor motifs) being tested.

This is located in a different directory than the clustering results, but follows the same structure, with each clustering separated into its own directory.

$ head -5 analysis/diffexp/kmeans_3_clusters/differential_expression.csv

Gene ID,Gene Name,Cluster 1 Mean UMI Counts,Cluster 1 Log2 fold change,Cluster 1 Adjusted p value,Cluster 2 Mean UMI Counts,Cluster 2 Log2 fold change,Cluster 2 Adjusted p value,Cluster 3 Mean UMI Counts,Cluster 3 Log2 fold change,Cluster 3 Adjusted p value
ENSG00000228327,RP11-206L10.2,0.0056858989363338264,2.6207666981569986,0.00052155805898912184,0.0,-0.75299726644507814,0.64066099091888962,0.00071455453829430329,-2.3725403666493312,0.0043023680184636837
ENSG00000237491,RP11-206L10.9,0.00012635330969630726,-0.31783275717885928,0.40959138980118809,0.0,3.8319652342760779,0.11986963938734894,0.0,0.56605908868652577,0.39910771338768203
ENSG00000177757,FAM87B,0.0,-2.9027952579000154,0.0,0.0,3.2470027335549219,0.19129034227967889,0.00071455453829430329,3.1510215894076818,0.0
ENSG00000225880,LINC00115,0.0003790599290889218,-5.71015017995762,8.4751637615375386e-28,0.20790015775229512,7.965820981010868,1.3374521290889345e-46,0.0017863863457357582,-2.2065304152104019,0.00059189960914085744