Guide to ggmanh Package
27 April 2022
Package
ggmanh 1.0.0
1 Introduction
The package ggmanh is aimed to provide easy and direct access to visualisation to the GWAS / PWAS results while also providing many functionalities and features.
Manhattan plot is commonly used to display significant Single Nucleotide Polymorphisms (SNPs) in Genome Wide Association Study (GWAS). The x-axis is divided into chromosomes, and SNPs are plotted in their respective positions. The y-axis typically represents \(-10*log(p value)\). Majority of the points have low y-values, with some of the significant SNPs having high y-values. It is not uncommon to see strong association between SNPs and a phenotype, yielding a high y-value. This results in a wide y-scales in which SNPs with lower significance are squished.
This function addresses this problem by rescaling the y-axis according to the range of y. There are more features, such as labelling without overlap (with the help of ggprepel package), reflecting the size of chromosomes along the x-axis, and displaying significant lines.
The package can be installed by:
if (!require("BiocManager"))
install.packages("BiocManager")
BiocManager::install("ggmanh")2 Functions Overview
manhattan_plot() is a generic method that can take a data.frame, MPdata, or a GRanges object. The data.frame, at bare minimum, must have three columns containing: chromosome, position, and p.value. For a GRanges object, meta data column name for the p-value needs to be passed.
There are two steps to this function: preprocess data and plot data. The preprocessing step (accomplished with manhattan_data_preprocess()) preprocesses the data by calculating the new x-position to map to the plot (new_pos column added to the data), “thining” the data points, and saving other graphical information needed for manhattan plot, which is returned as a MPdata object. The plot step (accomplished with manhattan_plot()) determines if rescaling of the y-axis is needed and plots / saves the manhattan plot.
While using manhattan_plot() on data.frame is sufficient, it is fine to separately run pre-processing and plotting for customizing the plot without having to preprocess again and again.
3 Example with Simulated GWAS
library(ggmanh)
#> Loading required package: ggplot2
library(SeqArray)
#> Loading required package: gdsfmtFirst, create a simulated data to be used for demonstration.
set.seed(1000)
nsim <- 50000
simdata <- data.frame(
"chromosome" = sample(c(1:22,"X"), size = nsim, replace = TRUE),
"position" = sample(1:100000000, size = nsim),
"P.value" = rbeta(nsim, shape1 = 5, shape2 = 1)^7
)manhattan_plot expects data.frame to have at least three columns: chromosome, position, and p.value.
head(simdata)
#> chromosome position P.value
#> 1 16 41575779 0.135933290
#> 2 4 73447172 0.764033749
#> 3 11 82120979 0.002440878
#> 4 22 94419970 0.644460838
#> 5 19 38141341 0.184945910
#> 6 3 43235060 0.774330251To avoid ambiguity in plotting, it is recommended that that the chromosome column is passed as a factor, or chr.order is specified.
simdata$chromosome <- factor(simdata$chromosome, c(1:22,"X"))This is the bare minimum to plot manhattan plot, and manhattan_plot can handle the rest.
g <- manhattan_plot(x = simdata, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position", plot.title = "Simulated P.Values", y.label = "P")
g
manhattan_plot is also defaulted to display the GWAS p.value threshold at 5e-8 and 5e-7. For now, the threshold is required; the values and color can be customized.
3.1 Rescaling
The function is also suited to rescale the y-axis depending on the magnitude of p values.
Let’s suppose that there are signals from chromosome 5 and 21, and the significant p-value is low for chromosome 21 and even lower for chromosome 5.
tmpdata <- data.frame(
"chromosome" = c(rep(5, 10), rep(21, 5)),
"position" = c(sample(250000:250100, 10, replace = FALSE), sample(590000:600000, 5, replace = FALSE)),
"P.value" = c(10^-(rnorm(10, 100, 3)), 10^-rnorm(5, 9, 1))
)
simdata <- rbind(simdata, tmpdata)
simdata$chromosome <- factor(simdata$chromosome, c(1:22,"X"))g <- manhattan_plot(x = simdata, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position", plot.title = "Simulated P.Values - Significant", rescale = FALSE)
g
The significant point at chromosome 5 has such a small p-value compared to other chromosomes that other significant poitns are less visible and the pattern at other chromosomes are masked. Rescaling attempts to fix this by changing the visual scale near the significant cutoff, removing the large white space in between.
g <- manhattan_plot(x = simdata, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position", plot.title = "Simulated P.Values - Significant", rescale = TRUE)
g
The place where jump happens is indicated on the y-axis by a double line (“=”).
3.2 Annotation
Annotation is also very simple. The function makes use of ggrepel’s geom_repel_label() to annotate each point while trying to avoid collision between texts.
All that is needed is to add a column containing labels. The function labels everything included in the column, so it is important to keep the labels for the points you are interested in, and set the rest with NA or "". From my understanding & experience, the differences between the two options are:
NA: The labels will likely not overlap, but may conceal the points. If there are a lot of points & labels, this is faster than using""."": The labels will avoid other labels as well as other points.
If you forget to do so and try to label all the points, the plotting may take hours.
sig <- simdata$P.value < 5e-07
simdata$label <- ""
simdata$label[sig] <- sprintf("Label: %i", 1:sum(sig))To add the labels to the plot, specify the column name with labels to label.colname. Also, you can change various aspects of the plot by with different arguments. To avoid having to preprocess over and over, you can separately preprocess first and then customize the plot.
simdata$label2 <- ""
i <- (simdata$chromosome == 5) & (simdata$P.value < 5e-8)
simdata$label2[i] <- paste("Chromosome 5 label", 1:sum(i))
mpdata <- manhattan_data_preprocess(x = simdata, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position")
g <- manhattan_plot(x = mpdata, label.colname = "label", plot.title = "Simulated P.Values with labels")
g
g <- manhattan_plot(x = mpdata, label.colname = "label2", label.font.size = 2, plot.title = "Simulated P.Values with labels", max.overlaps = Inf, force = 5)
g
3.3 Highlighting
You can also choose the colors for each point. You will need to add a column that categorizes the point to the data, and supply the column name to highlight.colname as well pass a character vector to highlight.col, which specifies the colop mapped to each value in highlight.colname. Then set color.by.highlight = TRUE.
You can see that you only have to preprocess the original data once while still making changes to the plot itself.
simdata$color <- "Not Significant"
simdata$color[simdata$P.value <= 5e-8] <- "Significant"
highlight_colormap <- c("Not Significant" = "grey", "Significant" = "black")
tmp <- manhattan_data_preprocess(
simdata, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position",
highlight.colname = "color", highlight.col = highlight_colormap
)
g_nohighlight <- manhattan_plot(tmp, plot.title = "No Highlight Points")
g <- manhattan_plot(tmp, plot.title = "Highlight Points", color.by.highlight = TRUE)
g_nohighlight
g
3.4 thinPoints
Another simple, yet useful, feature of the package is a function called thinPoints. The function can be called manually or used as a part of manhattan_data_preprocess. It will partition the \(log_{10}(pvalue)\) into nbin bins (manhattan_data_preprocess uses 200 bins to be conservative), and then randomly sample up to n points to effectively reduce the data while keeping the resulting output visually equal. This is done to keep the size of MPdata, which contains the data itself, small, and speed up the process of plotting.
3.5 Zoom into Chromosome
If a value is passed to chromosome argument of the function manhattan_plot or manhattan_data_preprocess, then the plot zooms into a chromosome if you are interested in a specific chromosome.
NOTE: When chromosome is specified, the default behavior is to turn off thinPoints as the default thin.n value may be too small and may make the plot less cluttered than it actually is. The user can manually increase thin.n so that the visual output is not changed dramatically while keeping the data size small.
manhattan_plot(simdata, chromosome = 5, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position")
4 Annotation with GDS File
The package also comes with a small GDS file in a SeqArray file format that contains chromosome, position, reference / alternate allele, and Ensembl Variant Effect Predictor of highest consequence. We obtained exomic data from the GnomAD database in VCF format, then converted to GDS file. Finally, some cleaning was done to get this final GDS file. The gds data that comes with this package can be located with this code after installation.
default_gds_path <- system.file("extdata", "gnomad.exomes.vep.hg19.v5.gds", mustWork = TRUE, package = "ggmanh")
print(default_gds_path)
gds <- SeqArray::seqOpen(default_gds_path)
print(gds)
SeqArray::seqClose(gds)The gds file contains position, chromosome, and allele (reference and alternate), which can be used to search variants. In this file, the gene symbol, consequence (by VEP), and the loss of function predictor (by LOFTEE) are stored in annotation/symbol, annotation/consequence, annnotation/LoF, respectively. We were able to keep the annotation data size small due to several reasons:
* We have removed RS IDs, which is stored in `annotation/id`. Although the gds file has the capabilities to store the RS IDs, we removed them to save space
* Each variant may have multiple Gene/Consequence predicted by VEP. For example, VEP predicts rs429358 to have an effect on APOE and TOMM40 genes. We've selected only one effect with the highest consequence in this case. Only one predicted effect is included for each variant.
* The VCF data format has been converted to a GDS data format.gds_annotate() is used to retrieve annotations.
sampledata <- data.frame(
chromosome = c(1, 17, 19, 22),
position = c(12422750, 10366900, 43439739, 39710145),
Reference = c("A", "T", "T", "G"),
Alternate = c("G", "G", "C", "A")
)
gds_annotate(
sampledata, annot.method = "position",
chr = "chromosome", pos = "position", ref = "Reference", alt = "Alternate"
)
#> Using default gds annotation file from ggmanh package. Run '?ggmanh_annotation_gds' for more information.
#> # of selected variants: 2
#> [1] "" "" "PSG7/missense" "RPL3/synonymous"Annotations are returned in the same order as the rows in the data.frame. If the parameter gdsfile is empty (NULL), then the default GDS file is used.
There are two ways to retrieve annotations. One way is to match the variants by chromosome, position, reference allele, and alternate allele. Another way is to match by RS ID (the RS ID needs to be stored in “annotation/id” in the annotation gds file. Look up documentation for SeqArray::seqSetFilterAnnotID for more detail).
Therefore, you can use gds_annotate to quickly add annotations to the GWAS summary results, and then plot manhattan plot with annotations.
simdata$Reference <- NA
simdata$Alternate <- NA
simdata <- simdata[,c("chromosome", "position", "Reference", "Alternate", "P.value")]
sampledata$P.value <- 10^-rnorm(4, 14, 1)
sampledata <- sampledata[c("chromosome", "position", "Reference", "Alternate", "P.value")]
simdata_label <- rbind(simdata, sampledata)
# add annotation
simdata_label$label <- gds_annotate(x = simdata_label, annot.method = "position", chr = "chromosome", pos = "position", ref = "Reference", alt = "Alternate")
#> Using default gds annotation file from ggmanh package. Run '?ggmanh_annotation_gds' for more information.
#> # of selected variants: 2
manhattan_plot(simdata_label, outfn = NULL, pval.colname = "P.value", chr.colname = "chromosome", pos.colname = "position", label.colname = "label")
5 SessionInfo
sessionInfo()
#> R version 4.2.0 RC (2022-04-19 r82224)
#> Platform: x86_64-pc-linux-gnu (64-bit)
#> Running under: Ubuntu 20.04.4 LTS
#>
#> Matrix products: default
#> BLAS: /home/biocbuild/bbs-3.15-bioc/R/lib/libRblas.so
#> LAPACK: /home/biocbuild/bbs-3.15-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] stats graphics grDevices utils datasets methods base
#>
#> other attached packages:
#> [1] SeqArray_1.36.0 gdsfmt_1.32.0 ggmanh_1.0.0 ggplot2_3.3.5
#> [5] BiocStyle_2.24.0
#>
#> loaded via a namespace (and not attached):
#> [1] ggrepel_0.9.1 Rcpp_1.0.8.3 Biostrings_2.64.0
#> [4] assertthat_0.2.1 digest_0.6.29 utf8_1.2.2
#> [7] R6_2.5.1 GenomeInfoDb_1.32.0 stats4_4.2.0
#> [10] evaluate_0.15 highr_0.9 pillar_1.7.0
#> [13] zlibbioc_1.42.0 rlang_1.0.2 jquerylib_0.1.4
#> [16] magick_2.7.3 S4Vectors_0.34.0 rmarkdown_2.14
#> [19] labeling_0.4.2 stringr_1.4.0 RCurl_1.98-1.6
#> [22] munsell_0.5.0 compiler_4.2.0 xfun_0.30
#> [25] pkgconfig_2.0.3 BiocGenerics_0.42.0 htmltools_0.5.2
#> [28] tidyselect_1.1.2 tibble_3.1.6 GenomeInfoDbData_1.2.8
#> [31] bookdown_0.26 IRanges_2.30.0 fansi_1.0.3
#> [34] crayon_1.5.1 dplyr_1.0.8 withr_2.5.0
#> [37] bitops_1.0-7 grid_4.2.0 jsonlite_1.8.0
#> [40] gtable_0.3.0 lifecycle_1.0.1 DBI_1.1.2
#> [43] magrittr_2.0.3 scales_1.2.0 cli_3.3.0
#> [46] stringi_1.7.6 farver_2.1.0 XVector_0.36.0
#> [49] bslib_0.3.1 ellipsis_0.3.2 generics_0.1.2
#> [52] vctrs_0.4.1 RColorBrewer_1.1-3 tools_4.2.0
#> [55] glue_1.6.2 purrr_0.3.4 parallel_4.2.0
#> [58] fastmap_1.1.0 yaml_2.3.5 colorspace_2.0-3
#> [61] BiocManager_1.30.17 GenomicRanges_1.48.0 knitr_1.39
#> [64] sass_0.4.1