Quality Control
8 February 2022
Quality Ranking
## [1] TRUESesame provide convenient function to compare your sample with public data sets processed with the same pipeline. All you need is a raw SigSet.
Quality Metrics
SeSAMe provides a set of quality control steps. Be sure to pre-cache HM450 annotation data from ExperimentHub. This only needs to be done once per sesame installation.
The SeSAMe QC function returns an sesameQC object which can be directly printed onto the screen.
##
## =======================
## = Intensities =
## =======================
## No. probes (num_probes_all) 866895
## mean (M/U) (mean_intensity): 2657.248
## mean (M+U) (mean_intensity_total): 5314.496
##
## -- Infinium II --
## No. probes: (num_probes_II) 724612 (83.587%)
## Mean Intensity (mean_ii): 2526.561
##
## -- Infinium I (Red) --
## No. probes: (num_probes_IR) 92294 (10.647%)
## No. Probes Consistent Channel: 92200
## No. Porbes Swapped Channel: 94
## No. Probes Low Intensity:
## Mean Intensity (in-band): 3579.385
## Mean Intensity (out-of-band): 524.6618
##
## -- Infinium I (Grn) --
## No. probes: 49989 (5.766%)
## No. Probes Consistent Channel: 49393
## No. Probes Swapped Channel: 596
## No. Probes Low Intensity:
## Mean Intensity (in-band): 2849.083
## Mean Intensity (out-of-band): 303.2474
##
## =======================
## = Non-detection =
## =======================
## No. probes: 33437
## No. probes w/ NA (num_na): 33437 (3.857%)
## No. nondetection (num_nondt): 33437 (3.857%)
##
## =======================
## = Beta Values =
## =======================
## Mean Betas: 0.5762464
## Median Betas: 0.7268695
##
## -- cg probes --
## No. Probes: 863904
## No. Probes with NA: 32886 (3.807%)
## Mean Betas: 0.5776934
## Median Betas: 0.7289541
## % Unmethylated (Beta < 0.3): 30.806%
## % Methylated (Beta > 0.7): 51.878%
##
## -- ch probes --
## No. Probes: 2932
## No. Probes with NA: 548 (18.690%)
## Mean Betas: 0.07323188
## Median Betas: 0.06114149
## % Unmethylated (Beta < 0.3): 99.874%
## % Methylated (Beta > 0.7): 0.000%
##
## -- rs probes --
## No. Probes: 59
## No. Probes with NA: 3 (5.085%)
## Mean Betas: 0.518126
## Median Betas: 0.5150823
## % Unmethylated (Beta < 0.3): 30.357%
## % Methylated (Beta > 0.7): 33.929%The sesameQC object can be coerced into data.frame and linked using the following code
qc5 <- do.call(rbind, lapply(sdfs, function(x)
as.data.frame(sesameQC(x))))
qc5$sample_name <- names(sdfs)
qc5[,c('mean_beta_cg','frac_meth_cg','frac_unmeth_cg')]Signal Background
The background level is given by mean_oob_grn and mean_oob_red
library(ggplot2)
ggplot(qc5,
aes(x = mean_oob_grn, y= mean_oob_red, label = sample_name)) +
geom_point() + geom_text(hjust = -0.1, vjust = 0.1) +
geom_abline(intercept = 0, slope = 1, linetype = 'dotted') +
xlab('Green Background') + ylab('Red Background') +
xlim(c(200,600)) + ylim(c(200,600))
Mean Intensity
The mean {M,U} intensity can be reached by mean_intensity. Similarly, the mean M+U intensity can be reached by mean_intensity_total. Low intensities are symptomatic of low input or poor hybridization.
library(wheatmap)
p1 <- ggplot(qc5) +
geom_bar(aes(sample_name, mean_intensity), stat='identity') +
xlab('Sample Name') + ylab('Mean Intensity') +
ylim(0,18000) +
theme(axis.text.x = element_text(angle=90, vjust=0.5, hjust=1))
p2 <- ggplot(qc5) +
geom_bar(aes(sample_name, mean_intensity_total), stat='identity') +
xlab('Sample Name') + ylab('Mean M+U Intensity') +
ylim(0,18000) +
theme(axis.text.x = element_text(angle=90, vjust=0.5, hjust=1))
WGG(p1) + WGG(p2, RightOf())
Probe Success Rate
The fraction of NAs are signs of masking due to variety of reasons including failed detection, high background, putative low quality probes etc. This number can be reached in frac_na_cg and num_na_cg (the cg stands for CpG probes, so we also have num_na_ch and num_na_rs)
p1 <- ggplot(qc5) +
geom_bar(aes(sample_name, num_na_cg), stat='identity') +
xlab('Sample Name') + ylab('Number of NAs') +
theme(axis.text.x = element_text(angle=90, vjust=0.5, hjust=1))
p2 <- ggplot(qc5) +
geom_bar(aes(sample_name, frac_na_cg), stat='identity') +
xlab('Sample Name') + ylab('Fraction of NAs (%)') +
theme(axis.text.x = element_text(angle=90, vjust=0.5, hjust=1))
WGG(p1) + WGG(p2, RightOf())
Color Channel Switch
The fraction of color channel switch can be found in InfI_switch_G2R and InfI_switch_R2G. These numbers are symptomatic of how Infinium I probes are affected by SNP-induced color channel switching.
Bisulfite Conversion
Infinium platforms are intrinsically robust to incomplete bisulfite conversion as non-converted probes would fail to hybridize to the target. Residual incomplete bisulfite conversion can be quantified using GCT score based on C/T-extension probes. Details of this method can be found in Zhou et al. 2017. The closer the score to 1.0, the more complete the bisulfite conversion.
## [1] 1.067769Extract Genotypes
SeSAMe can output explicit and Infinium-I-derived SNP to VCF. This information can be used to identify sample swaps.
## Retrieving annotation from https://zhouserver.research.chop.edu/InfiniumAnnotation/current/EPIC/EPIC.hg19.snp_overlap_b151.rds ... Done.## Retrieving annotation from https://zhouserver.research.chop.edu/InfiniumAnnotation/current/EPIC/EPIC.hg19.typeI_overlap_b151.rds ... Done.One can output to actual VCF file with a header by formatVCF(sdf, vcf=path_to_vcf).
Session Info
## R version 4.1.2 (2021-11-01)
## 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] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] wheatmap_0.1.0 ggplot2_3.3.5 sesame_1.12.9
## [4] sesameData_1.12.0 rmarkdown_2.11 ExperimentHub_2.2.1
## [7] AnnotationHub_3.2.1 BiocFileCache_2.2.1 dbplyr_2.1.1
## [10] BiocGenerics_0.40.0
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## loaded via a namespace (and not attached):
## [1] matrixStats_0.61.0 bitops_1.0-7
## [3] bit64_4.0.5 RColorBrewer_1.1-2
## [5] filelock_1.0.2 httr_1.4.2
## [7] GenomeInfoDb_1.30.1 tools_4.1.2
## [9] bslib_0.3.1 utf8_1.2.2
## [11] R6_2.5.1 KernSmooth_2.23-20
## [13] DBI_1.1.2 colorspace_2.0-2
## [15] withr_2.4.3 DNAcopy_1.68.0
## [17] tidyselect_1.1.1 gridExtra_2.3
## [19] preprocessCore_1.56.0 bit_4.0.4
## [21] curl_4.3.2 compiler_4.1.2
## [23] cli_3.1.1 Biobase_2.54.0
## [25] DelayedArray_0.20.0 labeling_0.4.2
## [27] sass_0.4.0 scales_1.1.1
## [29] randomForest_4.7-1 proxy_0.4-26
## [31] rappdirs_0.3.3 stringr_1.4.0
## [33] digest_0.6.29 XVector_0.34.0
## [35] pkgconfig_2.0.3 htmltools_0.5.2
## [37] MatrixGenerics_1.6.0 highr_0.9
## [39] fastmap_1.1.0 rlang_1.0.1
## [41] RSQLite_2.2.9 shiny_1.7.1
## [43] farver_2.1.0 jquerylib_0.1.4
## [45] generics_0.1.2 jsonlite_1.7.3
## [47] BiocParallel_1.28.3 dplyr_1.0.7
## [49] RCurl_1.98-1.5 magrittr_2.0.2
## [51] GenomeInfoDbData_1.2.7 Matrix_1.4-0
## [53] Rcpp_1.0.8 munsell_0.5.0
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## [57] lifecycle_1.0.1 stringi_1.7.6
## [59] yaml_2.2.2 MASS_7.3-55
## [61] SummarizedExperiment_1.24.0 zlibbioc_1.40.0
## [63] plyr_1.8.6 grid_4.1.2
## [65] blob_1.2.2 parallel_4.1.2
## [67] promises_1.2.0.1 ggrepel_0.9.1
## [69] crayon_1.4.2 lattice_0.20-45
## [71] Biostrings_2.62.0 KEGGREST_1.34.0
## [73] knitr_1.37 pillar_1.7.0
## [75] GenomicRanges_1.46.1 fgsea_1.20.0
## [77] reshape2_1.4.4 stats4_4.1.2
## [79] fastmatch_1.1-3 glue_1.6.1
## [81] BiocVersion_3.14.0 evaluate_0.14
## [83] data.table_1.14.2 BiocManager_1.30.16
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## [93] mime_0.12 xtable_1.8-4
## [95] e1071_1.7-9 later_1.3.0
## [97] class_7.3-20 tibble_3.1.6
## [99] AnnotationDbi_1.56.2 memoise_2.0.1
## [101] IRanges_2.28.0 ellipsis_0.3.2
## [103] interactiveDisplayBase_1.32.0 BiocStyle_2.22.0