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Tom
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@tom-10763
Last seen 5.2 years ago
Hi all,
I have several 450k and 850k (EPIC) array IDAT files. After combining them using minfi::combineArrays() and normalizing, I want to convert the object into MethyLumiSet class for downstream analysis.
Because no functions are implemented for that purpose, I tried to create a new MethyLumiSet inheriting the values from the combined MethylSet. However, I am not able to create a MethyLumiSet with some errors.
Is there a good way to achieve it?
> library(minfi) > library(methylumi) > illumina_epic=read.metharray.exp("~/My/EPICdata/directory/") > illumina_450k=read.metharray.exp("~/My/450Kdata/directory/") > comb=combineArrays(illumina_epic,illumina_450k,outType="IlluminaHumanMethylation450k") > GRset.norm=preprocessNoob(comb, offset = 15, dyeCorr = TRUE, verbose = TRUE,dyeMethod="single") > metLumi=new("MethyLumiSet",assayData=GRset.norm@assayData,phenoData=GRset.norm@phenoData,annotation=GRset.norm@annotation,betas=getBeta(GRset.norm)) Error in validObject(.Object) : invalid class "MethyLumiSet" object: 'AssayData' missing 'betas'
I tried another way, which also ended with an error.
> x=new("MethyLumiSet") > methylated(x) = getMeth(GRset.norm) Error in .validate_assayDataElementReplace(obj, value) : object and replacement value have different dimensions
> sessionInfo() R version 3.3.2 (2016-10-31) Platform: x86_64-apple-darwin13.4.0 (64-bit) Running under: OS X Mavericks 10.9.5 locale: [1] C attached base packages: [1] stats4 parallel stats graphics grDevices utils datasets methods base other attached packages: [1] methylumi_2.20.0 FDb.InfiniumMethylation.hg19_2.2.0 [3] org.Hs.eg.db_3.4.0 TxDb.Hsapiens.UCSC.hg19.knownGene_3.2.2 [5] GenomicFeatures_1.26.2 AnnotationDbi_1.36.0 [7] matrixStats_0.51.0 ggplot2_2.2.0 [9] reshape2_1.4.2 scales_0.4.1 [11] minfi_1.20.2 bumphunter_1.14.0 [13] locfit_1.5-9.1 iterators_1.0.8 [15] foreach_1.4.3 Biostrings_2.42.1 [17] XVector_0.14.0 SummarizedExperiment_1.4.0 [19] GenomicRanges_1.26.1 GenomeInfoDb_1.10.1 [21] IRanges_2.8.1 S4Vectors_0.12.1 [23] Biobase_2.34.0 BiocGenerics_0.20.0 loaded via a namespace (and not attached): [1] httr_1.2.1 nor1mix_1.2-2 splines_3.3.2 [4] assertthat_0.1 doRNG_1.6 Rsamtools_1.26.1 [7] RSQLite_1.1-1 lattice_0.20-34 limma_3.30.7 [10] quadprog_1.5-5 digest_0.6.10 RColorBrewer_1.1-2 [13] colorspace_1.3-2 preprocessCore_1.36.0 Matrix_1.2-7.1 [16] plyr_1.8.4 GEOquery_2.40.0 siggenes_1.48.0 [19] XML_3.98-1.5 biomaRt_2.30.0 genefilter_1.56.0 [22] zlibbioc_1.20.0 xtable_1.8-2 BiocParallel_1.8.1 [25] tibble_1.2 openssl_0.9.5 annotate_1.52.1 [28] beanplot_1.2 pkgmaker_0.22 lazyeval_0.2.0 [31] survival_2.40-1 magrittr_1.5 mclust_5.2 [34] memoise_1.0.0 nlme_3.1-128 MASS_7.3-45 [37] tools_3.3.2 registry_0.3 data.table_1.10.0 [40] stringr_1.1.0 munsell_0.4.3 rngtools_1.2.4 [43] base64_2.0 grid_3.3.2 RCurl_1.95-4.8 [46] bitops_1.0-6 gtable_0.2.0 codetools_0.2-15 [49] multtest_2.30.0 DBI_0.5-1 reshape_0.8.6 [52] R6_2.2.0 illuminaio_0.16.0 GenomicAlignments_1.10.0 [55] rtracklayer_1.34.1 stringi_1.1.2 Rcpp_0.12.8
I would appreciate any helps or comments.
Tom
also ended with the same error.
Any suggestion would be very welcome.