# 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 4.2.1 (2022-06-23) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Ubuntu 20.04.5 LTS Matrix products: default BLAS: /home/biocbuild/bbs-3.16-bioc/R/lib/libRblas.so LAPACK: /home/biocbuild/bbs-3.16-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_1.14.0 scran_1.26.0 [3] scater_1.26.0 ggplot2_3.3.6 [5] scuttle_1.8.0 ensembldb_2.22.0 [7] AnnotationFilter_1.22.0 GenomicFeatures_1.50.0 [9] AnnotationDbi_1.60.0 AnnotationHub_3.6.0 [11] BiocFileCache_2.6.0 dbplyr_2.2.1 [13] scRNAseq_2.11.0 SingleCellExperiment_1.20.0 [15] SummarizedExperiment_1.28.0 Biobase_2.58.0 [17] GenomicRanges_1.50.0 GenomeInfoDb_1.34.0 [19] IRanges_2.32.0 S4Vectors_0.36.0 [21] BiocGenerics_0.44.0 MatrixGenerics_1.10.0 [23] matrixStats_0.62.0 BiocStyle_2.26.0 [25] rebook_1.8.0 loaded via a namespace (and not attached): [1] igraph_1.3.5 lazyeval_0.2.2 [3] BiocParallel_1.32.0 digest_0.6.30 [5] htmltools_0.5.3 viridis_0.6.2 [7] fansi_1.0.3 magrittr_2.0.3 [9] memoise_2.0.1 ScaledMatrix_1.6.0 [11] cluster_2.1.4 limma_3.54.0 [13] Biostrings_2.66.0 prettyunits_1.1.1 [15] colorspace_2.0-3 blob_1.2.3 [17] rappdirs_0.3.3 ggrepel_0.9.1 [19] xfun_0.34 dplyr_1.0.10 [21] crayon_1.5.2 RCurl_1.98-1.9 [23] jsonlite_1.8.3 graph_1.76.0 [25] glue_1.6.2 gtable_0.3.1 [27] zlibbioc_1.44.0 XVector_0.38.0 [29] DelayedArray_0.24.0 scales_1.2.1 [31] edgeR_3.40.0 DBI_1.1.3 [33] Rcpp_1.0.9 viridisLite_0.4.1 [35] xtable_1.8-4 progress_1.2.2 [37] dqrng_0.3.0 bit_4.0.4 [39] rsvd_1.0.5 metapod_1.6.0 [41] httr_1.4.4 dir.expiry_1.6.0 [43] ellipsis_0.3.2 pkgconfig_2.0.3 [45] XML_3.99-0.12 farver_2.1.1 [47] CodeDepends_0.6.5 sass_0.4.2 [49] locfit_1.5-9.6 utf8_1.2.2 [51] labeling_0.4.2 tidyselect_1.2.0 [53] rlang_1.0.6 later_1.3.0 [55] munsell_0.5.0 BiocVersion_3.16.0 [57] tools_4.2.1 cachem_1.0.6 [59] cli_3.4.1 generics_0.1.3 [61] RSQLite_2.2.18 ExperimentHub_2.6.0 [63] evaluate_0.17 stringr_1.4.1 [65] fastmap_1.1.0 yaml_2.3.6 [67] knitr_1.40 bit64_4.0.5 [69] purrr_0.3.5 KEGGREST_1.38.0 [71] sparseMatrixStats_1.10.0 mime_0.12 [73] xml2_1.3.3 biomaRt_2.54.0 [75] compiler_4.2.1 beeswarm_0.4.0 [77] filelock_1.0.2 curl_4.3.3 [79] png_0.1-7 interactiveDisplayBase_1.36.0 [81] statmod_1.4.37 tibble_3.1.8 [83] bslib_0.4.0 stringi_1.7.8 [85] highr_0.9 bluster_1.8.0 [87] lattice_0.20-45 ProtGenerics_1.30.0 [89] Matrix_1.5-1 vctrs_0.5.0 [91] pillar_1.8.1 lifecycle_1.0.3 [93] BiocManager_1.30.19 jquerylib_0.1.4 [95] BiocNeighbors_1.16.0 cowplot_1.1.1 [97] bitops_1.0-7 irlba_2.3.5.1 [99] httpuv_1.6.6 rtracklayer_1.58.0 [101] R6_2.5.1 BiocIO_1.8.0 [103] bookdown_0.29 promises_1.2.0.1 [105] gridExtra_2.3 vipor_0.4.5 [107] codetools_0.2-18 assertthat_0.2.1 [109] rjson_0.2.21 withr_2.5.0 [111] GenomicAlignments_1.34.0 Rsamtools_2.14.0 [113] GenomeInfoDbData_1.2.9 parallel_4.2.1 [115] hms_1.1.2 grid_4.2.1 [117] beachmat_2.14.0 rmarkdown_2.17 [119] DelayedMatrixStats_1.20.0 Rtsne_0.16 [121] shiny_1.7.3 ggbeeswarm_0.6.0 [123] restfulr_0.0.15 ```