# Lawlor human pancreas (SMARTer) ## Introduction This performs an analysis of the @lawlor2017singlecell dataset, consisting of human pancreas cells from various donors. ## Data loading ```r library(scRNAseq) sce.lawlor <- LawlorPancreasData() ``` ```r library(AnnotationHub) edb <- AnnotationHub()[["AH73881"]] anno <- select(edb, keys=rownames(sce.lawlor), keytype="GENEID", columns=c("SYMBOL", "SEQNAME")) rowData(sce.lawlor) <- anno[match(rownames(sce.lawlor), anno[,1]),-1] ``` ## Quality control ```r unfiltered <- sce.lawlor ``` ```r library(scater) stats <- perCellQCMetrics(sce.lawlor, subsets=list(Mito=which(rowData(sce.lawlor)$SEQNAME=="MT"))) qc <- quickPerCellQC(stats, percent_subsets="subsets_Mito_percent", batch=sce.lawlor$`islet unos id`) sce.lawlor <- sce.lawlor[,!qc$discard] ``` ```r colData(unfiltered) <- cbind(colData(unfiltered), stats) unfiltered$discard <- qc$discard gridExtra::grid.arrange( plotColData(unfiltered, x="islet unos id", y="sum", colour_by="discard") + scale_y_log10() + ggtitle("Total count") + theme(axis.text.x = element_text(angle = 90)), plotColData(unfiltered, x="islet unos id", y="detected", colour_by="discard") + scale_y_log10() + ggtitle("Detected features") + theme(axis.text.x = element_text(angle = 90)), plotColData(unfiltered, x="islet unos id", y="subsets_Mito_percent", colour_by="discard") + ggtitle("Mito percent") + theme(axis.text.x = element_text(angle = 90)), ncol=2 ) ```
Distribution of each QC metric across cells from each donor of the Lawlor pancreas dataset. Each point represents a cell and is colored according to whether that cell was discarded.

(\#fig:unref-lawlor-qc-dist)Distribution of each QC metric across cells from each donor of the Lawlor pancreas dataset. Each point represents a cell and is colored according to whether that cell was discarded.

```r plotColData(unfiltered, x="sum", y="subsets_Mito_percent", colour_by="discard") + scale_x_log10() ```
Percentage of mitochondrial reads in each cell in the 416B dataset compared to the total count. Each point represents a cell and is colored according to whether that cell was discarded.

(\#fig:unref-lawlor-qc-comp)Percentage of mitochondrial reads in each cell in the 416B dataset compared to the total count. Each point represents a cell and is colored according to whether that cell was discarded.

```r colSums(as.matrix(qc)) ``` ``` ## low_lib_size low_n_features high_subsets_Mito_percent ## 9 5 25 ## discard ## 34 ``` ## Normalization ```r library(scran) set.seed(1000) clusters <- quickCluster(sce.lawlor) sce.lawlor <- computeSumFactors(sce.lawlor, clusters=clusters) sce.lawlor <- logNormCounts(sce.lawlor) ``` ```r summary(sizeFactors(sce.lawlor)) ``` ``` ## Min. 1st Qu. Median Mean 3rd Qu. Max. ## 0.295 0.781 0.963 1.000 1.182 2.629 ``` ```r plot(librarySizeFactors(sce.lawlor), sizeFactors(sce.lawlor), pch=16, xlab="Library size factors", ylab="Deconvolution factors", log="xy") ```
Relationship between the library size factors and the deconvolution size factors in the Lawlor pancreas dataset.

(\#fig:unref-lawlor-norm)Relationship between the library size factors and the deconvolution size factors in the Lawlor pancreas dataset.

## Variance modelling Using age as a proxy for the donor. ```r dec.lawlor <- modelGeneVar(sce.lawlor, block=sce.lawlor$`islet unos id`) chosen.genes <- getTopHVGs(dec.lawlor, n=2000) ``` ```r par(mfrow=c(4,2)) blocked.stats <- dec.lawlor$per.block for (i in colnames(blocked.stats)) { current <- blocked.stats[[i]] plot(current$mean, current$total, main=i, pch=16, cex=0.5, xlab="Mean of log-expression", ylab="Variance of log-expression") curfit <- metadata(current) curve(curfit$trend(x), col='dodgerblue', add=TRUE, lwd=2) } ```
Per-gene variance as a function of the mean for the log-expression values in the Lawlor pancreas dataset. Each point represents a gene (black) with the mean-variance trend (blue) fitted separately for each donor.

(\#fig:unnamed-chunk-4)Per-gene variance as a function of the mean for the log-expression values in the Lawlor pancreas dataset. Each point represents a gene (black) with the mean-variance trend (blue) fitted separately for each donor.

## Dimensionality reduction ```r library(BiocSingular) set.seed(101011001) sce.lawlor <- runPCA(sce.lawlor, subset_row=chosen.genes, ncomponents=25) sce.lawlor <- runTSNE(sce.lawlor, dimred="PCA") ``` ## Clustering ```r snn.gr <- buildSNNGraph(sce.lawlor, use.dimred="PCA") colLabels(sce.lawlor) <- factor(igraph::cluster_walktrap(snn.gr)$membership) ``` ```r table(colLabels(sce.lawlor), sce.lawlor$`cell type`) ``` ``` ## ## Acinar Alpha Beta Delta Ductal Gamma/PP None/Other Stellate ## 1 1 0 0 13 2 16 2 0 ## 2 0 1 76 1 0 0 0 0 ## 3 0 161 1 0 0 1 2 0 ## 4 0 1 0 1 0 0 5 19 ## 5 0 0 175 4 1 0 1 0 ## 6 22 0 0 0 0 0 0 0 ## 7 0 75 0 0 0 0 0 0 ## 8 0 0 0 1 20 0 2 0 ``` ```r table(colLabels(sce.lawlor), sce.lawlor$`islet unos id`) ``` ``` ## ## ACCG268 ACCR015A ACEK420A ACEL337 ACHY057 ACIB065 ACIW009 ACJV399 ## 1 8 2 2 4 4 4 9 1 ## 2 14 3 2 33 3 2 4 17 ## 3 36 23 14 13 14 14 21 30 ## 4 7 1 0 1 0 4 9 4 ## 5 34 10 4 39 7 23 24 40 ## 6 0 2 13 0 0 0 5 2 ## 7 32 12 0 5 6 7 4 9 ## 8 1 1 2 1 2 1 12 3 ``` ```r gridExtra::grid.arrange( plotTSNE(sce.lawlor, colour_by="label"), plotTSNE(sce.lawlor, colour_by="islet unos id"), ncol=2 ) ```
Obligatory $t$-SNE plots of the Lawlor pancreas dataset. Each point represents a cell that is colored by cluster (left) or batch (right).

(\#fig:unref-grun-tsne)Obligatory $t$-SNE plots of the Lawlor pancreas dataset. Each point represents a cell that is colored by cluster (left) or batch (right).

## Session Info {-}
``` R version 4.1.1 (2021-08-10) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Ubuntu 20.04.3 LTS Matrix products: default BLAS: /home/biocbuild/bbs-3.14-bioc/R/lib/libRblas.so LAPACK: /home/biocbuild/bbs-3.14-bioc/R/lib/libRlapack.so locale: [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C [3] LC_TIME=en_GB LC_COLLATE=C [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8 [7] LC_PAPER=en_US.UTF-8 LC_NAME=C [9] LC_ADDRESS=C LC_TELEPHONE=C [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C attached base packages: [1] stats4 stats graphics grDevices utils datasets methods [8] base other attached packages: [1] BiocSingular_1.10.0 scran_1.22.0 [3] scater_1.22.0 ggplot2_3.3.5 [5] scuttle_1.4.0 ensembldb_2.18.0 [7] AnnotationFilter_1.18.0 GenomicFeatures_1.46.0 [9] AnnotationDbi_1.56.0 AnnotationHub_3.2.0 [11] BiocFileCache_2.2.0 dbplyr_2.1.1 [13] scRNAseq_2.7.2 SingleCellExperiment_1.16.0 [15] SummarizedExperiment_1.24.0 Biobase_2.54.0 [17] GenomicRanges_1.46.0 GenomeInfoDb_1.30.0 [19] IRanges_2.28.0 S4Vectors_0.32.0 [21] BiocGenerics_0.40.0 MatrixGenerics_1.6.0 [23] matrixStats_0.61.0 BiocStyle_2.22.0 [25] rebook_1.4.0 loaded via a namespace (and not attached): [1] igraph_1.2.7 lazyeval_0.2.2 [3] BiocParallel_1.28.0 digest_0.6.28 [5] htmltools_0.5.2 viridis_0.6.2 [7] fansi_0.5.0 magrittr_2.0.1 [9] memoise_2.0.0 ScaledMatrix_1.2.0 [11] cluster_2.1.2 limma_3.50.0 [13] Biostrings_2.62.0 prettyunits_1.1.1 [15] colorspace_2.0-2 blob_1.2.2 [17] rappdirs_0.3.3 ggrepel_0.9.1 [19] xfun_0.27 dplyr_1.0.7 [21] crayon_1.4.1 RCurl_1.98-1.5 [23] jsonlite_1.7.2 graph_1.72.0 [25] glue_1.4.2 gtable_0.3.0 [27] zlibbioc_1.40.0 XVector_0.34.0 [29] DelayedArray_0.20.0 scales_1.1.1 [31] edgeR_3.36.0 DBI_1.1.1 [33] Rcpp_1.0.7 viridisLite_0.4.0 [35] xtable_1.8-4 progress_1.2.2 [37] dqrng_0.3.0 bit_4.0.4 [39] rsvd_1.0.5 metapod_1.2.0 [41] httr_1.4.2 dir.expiry_1.2.0 [43] ellipsis_0.3.2 pkgconfig_2.0.3 [45] XML_3.99-0.8 farver_2.1.0 [47] CodeDepends_0.6.5 sass_0.4.0 [49] locfit_1.5-9.4 utf8_1.2.2 [51] tidyselect_1.1.1 labeling_0.4.2 [53] rlang_0.4.12 later_1.3.0 [55] munsell_0.5.0 BiocVersion_3.14.0 [57] tools_4.1.1 cachem_1.0.6 [59] generics_0.1.1 RSQLite_2.2.8 [61] ExperimentHub_2.2.0 evaluate_0.14 [63] stringr_1.4.0 fastmap_1.1.0 [65] yaml_2.2.1 knitr_1.36 [67] bit64_4.0.5 purrr_0.3.4 [69] KEGGREST_1.34.0 sparseMatrixStats_1.6.0 [71] mime_0.12 xml2_1.3.2 [73] biomaRt_2.50.0 compiler_4.1.1 [75] beeswarm_0.4.0 filelock_1.0.2 [77] curl_4.3.2 png_0.1-7 [79] interactiveDisplayBase_1.32.0 statmod_1.4.36 [81] tibble_3.1.5 bslib_0.3.1 [83] stringi_1.7.5 highr_0.9 [85] bluster_1.4.0 lattice_0.20-45 [87] ProtGenerics_1.26.0 Matrix_1.3-4 [89] vctrs_0.3.8 pillar_1.6.4 [91] lifecycle_1.0.1 BiocManager_1.30.16 [93] jquerylib_0.1.4 BiocNeighbors_1.12.0 [95] cowplot_1.1.1 bitops_1.0-7 [97] irlba_2.3.3 httpuv_1.6.3 [99] rtracklayer_1.54.0 R6_2.5.1 [101] BiocIO_1.4.0 bookdown_0.24 [103] promises_1.2.0.1 gridExtra_2.3 [105] vipor_0.4.5 codetools_0.2-18 [107] assertthat_0.2.1 rjson_0.2.20 [109] withr_2.4.2 GenomicAlignments_1.30.0 [111] Rsamtools_2.10.0 GenomeInfoDbData_1.2.7 [113] parallel_4.1.1 hms_1.1.1 [115] grid_4.1.1 beachmat_2.10.0 [117] rmarkdown_2.11 DelayedMatrixStats_1.16.0 [119] Rtsne_0.15 shiny_1.7.1 [121] ggbeeswarm_0.6.0 restfulr_0.0.13 ```