# 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 4.3.1 (2023-06-16) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Ubuntu 22.04.3 LTS Matrix products: default BLAS: /home/biocbuild/bbs-3.18-bioc/R/lib/libRblas.so LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0 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 time zone: America/New_York tzcode source: system (glibc) attached base packages: [1] stats4 stats graphics grDevices utils datasets methods [8] base other attached packages: [1] BiocSingular_1.18.0 scran_1.30.0 [3] scater_1.30.0 ggplot2_3.4.4 [5] scuttle_1.12.0 ensembldb_2.26.0 [7] AnnotationFilter_1.26.0 GenomicFeatures_1.54.0 [9] AnnotationDbi_1.64.0 AnnotationHub_3.10.0 [11] BiocFileCache_2.10.0 dbplyr_2.3.4 [13] Matrix_1.6-1.1 scRNAseq_2.15.0 [15] SingleCellExperiment_1.24.0 SummarizedExperiment_1.32.0 [17] Biobase_2.62.0 GenomicRanges_1.54.0 [19] GenomeInfoDb_1.38.0 IRanges_2.36.0 [21] S4Vectors_0.40.0 BiocGenerics_0.48.0 [23] MatrixGenerics_1.14.0 matrixStats_1.0.0 [25] BiocStyle_2.30.0 rebook_1.12.0 loaded via a namespace (and not attached): [1] rstudioapi_0.15.0 jsonlite_1.8.7 [3] CodeDepends_0.6.5 magrittr_2.0.3 [5] ggbeeswarm_0.7.2 farver_2.1.1 [7] rmarkdown_2.25 BiocIO_1.12.0 [9] zlibbioc_1.48.0 vctrs_0.6.4 [11] memoise_2.0.1 Rsamtools_2.18.0 [13] DelayedMatrixStats_1.24.0 RCurl_1.98-1.12 [15] htmltools_0.5.6.1 S4Arrays_1.2.0 [17] progress_1.2.2 curl_5.1.0 [19] BiocNeighbors_1.20.0 SparseArray_1.2.0 [21] sass_0.4.7 bslib_0.5.1 [23] cachem_1.0.8 GenomicAlignments_1.38.0 [25] igraph_1.5.1 mime_0.12 [27] lifecycle_1.0.3 pkgconfig_2.0.3 [29] rsvd_1.0.5 R6_2.5.1 [31] fastmap_1.1.1 GenomeInfoDbData_1.2.11 [33] shiny_1.7.5.1 digest_0.6.33 [35] colorspace_2.1-0 dqrng_0.3.1 [37] irlba_2.3.5.1 ExperimentHub_2.10.0 [39] RSQLite_2.3.1 beachmat_2.18.0 [41] labeling_0.4.3 filelock_1.0.2 [43] fansi_1.0.5 httr_1.4.7 [45] abind_1.4-5 compiler_4.3.1 [47] bit64_4.0.5 withr_2.5.1 [49] BiocParallel_1.36.0 viridis_0.6.4 [51] DBI_1.1.3 biomaRt_2.58.0 [53] rappdirs_0.3.3 DelayedArray_0.28.0 [55] bluster_1.12.0 rjson_0.2.21 [57] tools_4.3.1 vipor_0.4.5 [59] beeswarm_0.4.0 interactiveDisplayBase_1.40.0 [61] httpuv_1.6.12 glue_1.6.2 [63] restfulr_0.0.15 promises_1.2.1 [65] grid_4.3.1 Rtsne_0.16 [67] cluster_2.1.4 generics_0.1.3 [69] gtable_0.3.4 hms_1.1.3 [71] metapod_1.10.0 ScaledMatrix_1.10.0 [73] xml2_1.3.5 utf8_1.2.4 [75] XVector_0.42.0 ggrepel_0.9.4 [77] BiocVersion_3.18.0 pillar_1.9.0 [79] stringr_1.5.0 limma_3.58.0 [81] later_1.3.1 dplyr_1.1.3 [83] lattice_0.22-5 rtracklayer_1.62.0 [85] bit_4.0.5 tidyselect_1.2.0 [87] locfit_1.5-9.8 Biostrings_2.70.0 [89] knitr_1.44 gridExtra_2.3 [91] bookdown_0.36 ProtGenerics_1.34.0 [93] edgeR_4.0.0 xfun_0.40 [95] statmod_1.5.0 stringi_1.7.12 [97] lazyeval_0.2.2 yaml_2.3.7 [99] evaluate_0.22 codetools_0.2-19 [101] tibble_3.2.1 BiocManager_1.30.22 [103] graph_1.80.0 cli_3.6.1 [105] xtable_1.8-4 munsell_0.5.0 [107] jquerylib_0.1.4 Rcpp_1.0.11 [109] dir.expiry_1.10.0 png_0.1-8 [111] XML_3.99-0.14 parallel_4.3.1 [113] ellipsis_0.3.2 blob_1.2.4 [115] prettyunits_1.2.0 sparseMatrixStats_1.14.0 [117] bitops_1.0-7 viridisLite_0.4.2 [119] scales_1.2.1 purrr_1.0.2 [121] crayon_1.5.2 rlang_1.1.1 [123] cowplot_1.1.1 KEGGREST_1.42.0 ```