This vignette provides several practical demonstrations of how to use HM450K and EPIC platform CpG probe annotations, which are provided in the platform-specific manifests. These examples are shown for an example RGChannelSet using functions from the minfi package.

Probe manifest background

The CpG probe manifest files were provided by Illumina and contain a number of useful fields pertaining to the genome location of a CpG probe. When we read DNAm IDAT files into a SummarizedExperiment object using the minfi package (e.g. using read.metharray.exp() or similar), they are automatically combined with an array platform manifest containing rich probe-level details about the probe chemistry, the genome location, and various functional features and annotations to be aware of.

Getting the HM450K manifest annotations from an `RGChannelSet`

We can easily access the manifest of the older HM450K platform. Using an example RGChannelSet object from the minfiData package, we can extract and inspect the full HM450K platform manifest with getAnnotation() as follows:

rg <- get(data("RGsetEx"))
man <- as.data.frame(getAnnotation(rg))
colnames(man)

##  [1] "chr"                      "pos"                     
##  [3] "strand"                   "Name"                    
##  [5] "AddressA"                 "AddressB"                
##  [7] "ProbeSeqA"                "ProbeSeqB"               
##  [9] "Type"                     "NextBase"                
## [11] "Color"                    "Probe_rs"                
## [13] "Probe_maf"                "CpG_rs"                  
## [15] "CpG_maf"                  "SBE_rs"                  
## [17] "SBE_maf"                  "Islands_Name"            
## [19] "Relation_to_Island"       "Forward_Sequence"        
## [21] "SourceSeq"                "Random_Loci"             
## [23] "Methyl27_Loci"            "UCSC_RefGene_Name"       
## [25] "UCSC_RefGene_Accession"   "UCSC_RefGene_Group"      
## [27] "Phantom"                  "DMR"                     
## [29] "Enhancer"                 "HMM_Island"              
## [31] "Regulatory_Feature_Name"  "Regulatory_Feature_Group"
## [33] "DHS"

Array platform manifests are made available in the Bioconductor packages IlluminaHumanMethylation450kmanifest and IlluminaHumanMethylationEPICmanifest, so be sure to have these installed before working with DNAm arrays as SummarizedExperiment objects. These manifests are unchanged from the original manifest files, which can be accessed from Illumina’s website. The HM450K manifest can be found here, and the EPIC manifest can be found here. The official documents also include detailed descriptions of the manifest columns.

Getting the EPIC manifest annotations from an `RGChannelSet`

The newer EPIC platform contains a manifest with updated probe information, including several new annotation columns useful for probe filters.

rg.epic <- get(data("RGsetEPIC"))
man.epic <- as.data.frame(getAnnotation(rg.epic))
colnames(man.epic)

##  [1] "chr"                                  
##  [2] "pos"                                  
##  [3] "strand"                               
##  [4] "Name"                                 
##  [5] "AddressA"                             
##  [6] "AddressB"                             
##  [7] "ProbeSeqA"                            
##  [8] "ProbeSeqB"                            
##  [9] "Type"                                 
## [10] "NextBase"                             
## [11] "Color"                                
## [12] "Probe_rs"                             
## [13] "Probe_maf"                            
## [14] "CpG_rs"                               
## [15] "CpG_maf"                              
## [16] "SBE_rs"                               
## [17] "SBE_maf"                              
## [18] "Islands_Name"                         
## [19] "Relation_to_Island"                   
## [20] "Forward_Sequence"                     
## [21] "SourceSeq"                            
## [22] "UCSC_RefGene_Name"                    
## [23] "UCSC_RefGene_Accession"               
## [24] "UCSC_RefGene_Group"                   
## [25] "Phantom4_Enhancers"                   
## [26] "Phantom5_Enhancers"                   
## [27] "DMR"                                  
## [28] "X450k_Enhancer"                       
## [29] "HMM_Island"                           
## [30] "Regulatory_Feature_Name"              
## [31] "Regulatory_Feature_Group"             
## [32] "GencodeBasicV12_NAME"                 
## [33] "GencodeBasicV12_Accession"            
## [34] "GencodeBasicV12_Group"                
## [35] "GencodeCompV12_NAME"                  
## [36] "GencodeCompV12_Accession"             
## [37] "GencodeCompV12_Group"                 
## [38] "DNase_Hypersensitivity_NAME"          
## [39] "DNase_Hypersensitivity_Evidence_Count"
## [40] "OpenChromatin_NAME"                   
## [41] "OpenChromatin_Evidence_Count"         
## [42] "TFBS_NAME"                            
## [43] "TFBS_Evidence_Count"                  
## [44] "Methyl27_Loci"                        
## [45] "Methyl450_Loci"                       
## [46] "Random_Loci"

Annotation-based probe filters

There are many reasons we may want to filter or remove a CpG probe prior to performing downstream analyses such as differential methylation tests or epigenome-wide association tests. For instance, it is common to filter CpG probes which are likely to be impacted by underlying population genetic variation, or probes which have consistent poor quality. Two common reasons to filter probes are , or based on studies showing extensive cross-reactivity that limits a probe’s reliability. We can see how to perform these filters below.

Filtering on common SNPs

We can filter a probe based on high likelihood of a confounding single nucleotide polymorphism (SNP), or a variant that occurs near a probe (e.g. within the 50bp annealing sequence), or if it overlaps the exact CpG location. These probe-proximal SNPs can be identified either from the manifest (see above), or accessed independently using getSnpInfo(). For instance:

getSnpInfo(rg)

## DataFrame with 485512 rows and 6 columns
##                    Probe_rs Probe_maf      CpG_rs   CpG_maf      SBE_rs
##                 <character> <numeric> <character> <numeric> <character>
## cg00050873               NA        NA          NA        NA          NA
## cg00212031               NA        NA          NA        NA          NA
## cg00213748               NA        NA          NA        NA          NA
## cg00214611               NA        NA          NA        NA          NA
## cg00455876               NA        NA          NA        NA          NA
## ...                     ...       ...         ...       ...         ...
## ch.22.909671F            NA        NA          NA        NA          NA
## ch.22.46830341F          NA        NA          NA        NA          NA
## ch.22.1008279F           NA        NA          NA        NA          NA
## ch.22.47579720R  rs79009754  0.012587          NA        NA          NA
## ch.22.48274842R  rs79812973  0.022589          NA        NA          NA
##                   SBE_maf
##                 <numeric>
## cg00050873             NA
## cg00212031             NA
## cg00213748             NA
## cg00214611             NA
## cg00455876             NA
## ...                   ...
## ch.22.909671F          NA
## ch.22.46830341F        NA
## ch.22.1008279F         NA
## ch.22.47579720R        NA
## ch.22.48274842R        NA

It is recommended that CpG probes which contain a common SNP be filtered prior to analysis. Common SNPs are identified based on their minor allele frequency (MAF, e.g. from columns Probe_maf, CpG_maf, or SBE_maf).

The function dropLociWithSnps() allows one to filter a mapped MethylSet or RatioSet based on the SNP MAF frequency. For example:

gm <- preprocessRaw(rg) # make MethylSet
gms <- mapToGenome(gm) # make GenomicMethylSet
gmsf <- dropLociWithSnps(gms) # filter probes with SNPs

The minimum MAF frequency filter can be changed in dropLociWithSnps() by setting the maf argument. See ?dropLociWithSnps for details. Also note the SNP information is a product of its reference, and details about the specific genetic variant databases mined for this SNP info can be found in the manifest documentation (see above).

Filtering on cross-reactive CpG probes

A number of probes on both the EPIC and HM450K platforms were previously found to possess high cross-reactivity, an undesirable quality that limits probe measurement reliability. We can identify and remove probes with evidence of cross-reactivity from either platform by simply filtering on the identifiers of the probes to be removed. Several commonly utilized sources of CpG IDs for cross-reactive probes include:

Chen et al 2013 cross-reactive HM450K probes (source). Note, these probes have been uploaded here.
Pidsley et al 2016 cross-reactive EPIC probes (source). Note, these probes have also been uploaded here.

Access lists of cross-reactive probes with the recountmethylation function using get_crossreactive_cpgs() (see ?get_crossreactive_cpgs for details).

Querying and quantifying genome regions and functional groups

Many DNAm studies note whether methylation occurs in a gene’s promoter or body region. One reason is that we expect the functional consequences of DNAm to vary given its location in a gene, or indeed if it occurs in a gene at all. Another common way to annotate CpG probes is according to their position relative to protein-coding gene regions as well as relative to cytosine- and guanine-dense regions called CG Islands. We can quickly group probes according to either their gene or CG Island region using information in the manifest, as shown below.

Find probes mapping to a gene

The gene IDs can be found under the columns UCSC_RefGene_Name (for the common gene name) and UCSC_RefGene_Accession (for the official RefGene accession). Note that entries in these columns correspond to transcript labels, so gene names and IDs may be repeated multiple times separated by a semi-colon character. This formatting means we need to use regular expression to isolate all the probes by a given gene name.

We can quantify the number of intergenic (non-gene-mapping) and genic (gene-mapping) probes with:

as.data.frame(table(man$UCSC_RefGene_Name==""))

##    Var1   Freq
## 1 FALSE 365860
## 2  TRUE 119652

We can further grab all probes mapping to the gene ARID1A using:

gene.str <- "ARID1A" # common gene name
gene.patt <- paste0("(^|;)", gene.str, "($|;)") # regex pattern
which.gene <- which(grepl(gene.patt, man$UCSC_RefGene_Name)) # gene filter
manf <- man[which.gene,]
dim(manf)

## [1] 29 33

Viewing gene functional region frequencies

We can find the gene relation annotations under the column UCSC_RefGene_Group in the manifest. Values under this column are either blank, if a probe does not map to a gene (a.k.a. “intergenic probes”), or contains one or more location annotations corresponding to various overlapping transcript IDs.

To get all mapped gene regions as a vector, use:

gene.regionv <- unlist(strsplit(man$UCSC_RefGene_Group, ";"))

To view all possible group values, we can use:

unique(gene.regionv)

## [1] "Body"    "TSS1500" "TSS200"  "1stExon" "5'UTR"   "3'UTR"

To view the frequency with which each region is mapped by an array probe, use:

df <- as.data.frame(table(gene.regionv)) # get group frequencies
ggplot(df, aes(x = gene.regionv, y = Freq, fill = gene.regionv)) + theme_bw() +
  geom_bar( stat = "identity") + xlab("Gene group") + ylab("Num. probes") +
  theme(legend.position = "none",
        axis.text.x = element_text(angle = 45, hjust = 1))

Identifying promoter-mapping and gene body-mapping CpG probes

We can use this logic of the UCSC_RefGene_Group variable to build conditions for new functional regions of interest, namely promoter and gene body regions.

For promoters, we can use a common definition of a probe that maps to either the 5'UTR, TSS1500, or TSS200 annotation labels. We can make the new promoter variable using:

# make pattern: "(^|;)5'UTR($|;)|(^|;)TSS1500($|;)|(^|;)TSS200($|;)"
prom.catv <- c("5'UTR", "TSS1500", "TSS200")
prom.patt <- paste0("(^|;)", prom.catv, "($|;)", collapse = "|")
# use regex to detect promoter-mapping probes
man$promoter <- ifelse(grepl(prom.patt, man$UCSC_RefGene_Group),
                       TRUE, FALSE)
as.data.frame(table(man$promoter))

##    Var1   Freq
## 1 FALSE 295988
## 2  TRUE 189524

One way we can define the gene body is as all gene-mapping probes which don’t map to the gene promoter. Using a similar strategy as for the new promoter variable, we can define a new gene_body variable with:

# make pattern: "(^|;)Body($|;)|(^|;)3'UTR($|;)"
body.catv <- c("Body", "3'UTR")
body.patt <- paste0("(^|;)", body.catv, "($|;)", collapse = "|")
# use regex to detect body-mapping probes
man$gene_body <- ifelse(grepl(body.patt, man$UCSC_RefGene_Group),
                       TRUE, FALSE)
table(man$gene_body)

## 
##  FALSE   TRUE 
## 292622 192890

Since the manifest is transcript-centric, you will find that some probes map to the promoter of one transcript and the body of another transcript. You can view these as follows:

dfp <- as.data.frame(table(man$gene_body, man$promoter))
dfp$region <- c("intergenic", "body-only", "promoter-only", "body-and-promoter")
ggplot(dfp, aes(x = region, y = Freq, fill = region)) + theme_bw() +
  geom_bar( stat = "identity") + xlab("Gene region") + ylab("Num. probes") +
  theme(legend.position = "none",
        axis.text.x = element_text(angle = 45, hjust = 1))

CG Island annotations

It is comparatively straightforward to view a probe’s relation to a CG Island from the manifest using the variable Relation_to_Island. Unlike with the transcript-centric gene annotations, values in this variable occur 1:1 with probe IDs, as only one category applies to any given genome coordinate location.

We can see the unique categories for this variable from the manifest using:

unique(man$Relation_to_Island)

## [1] "N_Shore" "Island"  "S_Shore" "OpenSea" "N_Shelf" "S_Shelf"

Categories in Relation_to_Island are defined in the official documentation as:

Island : CG Island, a region with high cytosine- and guaning content. If a probe maps to a CG Island, the island name/coordinates can be found in the column Islands_Name.
N_Shore/S_Shore : The upstream (5’/North) and downstream (3’/South) shore regions. These are up to 2kbp-wide regions flanking CG islands.
N_Shelf/S_Shelf : The upstream (5’/North) and downstream (3’/South) shelf regions. These are 2-4kbp-wide regions flanking CG Islands and their shores.
OpenSea : Any regions occurring between CG islands.

We can plot the frequency of relative CG Island locations across HM450K array probes as follows:

dfp <- as.data.frame(table(man$Relation_to_Island))
ggplot(dfp, aes(x = Var1, y = Freq, fill = Var1)) + theme_bw() +
  geom_bar(stat = "identity") + xlab("Relation_to_Island") + ylab("Num. probes") +
  theme(legend.position = "none",
        axis.text.x = element_text(angle = 45, hjust = 1))

It is also easy to add the “genic” information, or whether a probe maps to a gene, alongside the CG Island annotations, as follows:

dfp <- as.data.frame(table(man$Relation_to_Island, man$UCSC_RefGene_Name==""))
dfp$region <- paste0(dfp$Var1," ; ", c(rep("genic", 6), rep("intergenic", 6)))
ggplot(dfp, aes(x = region, y = Freq, fill = Var1)) + theme_bw() +
  geom_bar(stat = "identity") + xlab("Relation_to_Island;Genic_status") + 
  ylab("Num. probes") +
  theme(legend.position = "none", 
        axis.text.x = element_text(angle = 45, hjust = 1))

Conclusions

This vignette described practical uses for the platform-specific, manifest-based annotations for CpG probes on HM450K and EPIC platforms.

Additional resources, information, and guidance for analyzing compilations of DNAm array datasets can be found in the following vignettes:

recountmethylation R/Bioconductor package documentation
minfi R/Bioconductor package and documentation
Illumina’s EPIC array documentation This official resource includes helpful descriptions of manifest columns in the file called infinium-methylationepic-manifest-column-headings.pdf.

Practical uses for provided CpG probe annotations