Entering edit mode
Hello,
I am using DRIMSeq to conduct differential splicing analyses from RNAseq data run with Salmon. unfortunately, I have encountered the below problem. It seems like there are issues with the filtering function. I have tried different parameters but even the simple 0 (meaning no filtering at all) given an error.
Any help and appreciation on how to overcome this is welcome. Thanks, Gaia
> d
#An object of class dmDSdata
#with 24916 genes and 6 samples
#* data accessors: counts(), samples()
> n <- 6
> n.small <- 1
> d <- dmFilter(d,
+ min_samps_feature_expr=n.small, min_feature_expr=1,
+ min_samps_feature_prop=n.small, min_feature_prop=0.1,
+ min_samps_gene_expr=n, min_gene_expr=1)
#Error in dmDS_filter(counts = x@counts, min_samps_gene_expr = min_samps_gene_expr, :
# !No genes left after filtering!
> n <- 0
> n.small <- 0
> d <- dmFilter(d,
+ min_samps_feature_expr=n.small, min_feature_expr=1,
+ min_samps_feature_prop=n.small, min_feature_prop=0.1,
+ min_samps_gene_expr=n, min_gene_expr=1)
#Error in dmDS_filter(counts = x@counts, min_samps_gene_expr = min_samps_gene_expr, :
# !No genes left after filtering!
> sessionInfo( )
> sessionInfo( )
R version 3.5.1 (2018-07-02)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: CentOS Linux 7 (Core)
Matrix products: default
BLAS: /bifx/apps/spack/spack-20190717/opt/spack/linux-centos7-x86_64/gcc-8.2.0/r-3.5.1-sgjamjmaepz56jr3vyephqqefmesazby/rlib/R/lib/libRblas.so
LAPACK: /bifx/apps/spack/spack-20190717/opt/spack/linux-centos7-x86_64/gcc-8.2.0/r-3.5.1-sgjamjmaepz56jr3vyephqqefmesazby/rlib/R/lib/libRlapack.so
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8 LC_MONETARY=en_US.UTF-8
[6] LC_MESSAGES=en_US.UTF-8 LC_PAPER=en_US.UTF-8 LC_NAME=C LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats4 parallel stats graphics grDevices utils datasets methods base
other attached packages:
[1] GenomicFeatures_1.34.1 EnhancedVolcano_1.0.1 ggrepel_0.8.0 ggplot2_3.1.0 dplyr_1.0.5
[6] biobroom_1.14.0 broom_0.5.1 dbplyr_1.3.0 pheatmap_1.0.12 annotables_0.1.91
[11] DEXSeq_1.28.3 RColorBrewer_1.1-2 AnnotationDbi_1.44.0 DESeq2_1.22.2 SummarizedExperiment_1.12.0
[16] DelayedArray_0.8.0 matrixStats_0.54.0 GenomicRanges_1.34.0 GenomeInfoDb_1.18.1 IRanges_2.16.0
[21] S4Vectors_0.20.1 Biobase_2.42.0 BiocGenerics_0.28.0 BiocParallel_1.16.5 DRIMSeq_1.10.1
loaded via a namespace (and not attached):
[1] colorspace_1.4-0 hwriter_1.3.2 ellipsis_0.3.1 htmlTable_1.13.1 XVector_0.22.0
[6] base64enc_0.1-3 rstudioapi_0.9.0 bit64_0.9-7 fansi_0.4.0 splines_3.5.1
[11] geneplotter_1.60.0 knitr_1.21 Formula_1.2-3 Rsamtools_1.34.0 annotate_1.60.0
[16] cluster_2.0.7-1 compiler_3.5.1 httr_1.4.0 backports_1.1.3 assertthat_0.2.0
[21] Matrix_1.2-15 lazyeval_0.2.1 limma_3.38.3 cli_1.1.0 acepack_1.4.1
[26] htmltools_0.3.6 prettyunits_1.0.2 tools_3.5.1 gtable_0.2.0 glue_1.4.1.9000
[31] GenomeInfoDbData_1.2.0 reshape2_1.4.3 Rcpp_1.0.0 vctrs_0.3.6 Biostrings_2.50.2
[36] nlme_3.1-137 rtracklayer_1.42.1 xfun_0.4 stringr_1.3.1 lifecycle_1.0.0
[41] statmod_1.4.32 XML_3.98-1.16 edgeR_3.24.3 zlibbioc_1.28.0 scales_1.0.0
[46] hms_0.4.2 yaml_2.2.0 memoise_1.1.0 gridExtra_2.3 biomaRt_2.38.0
[51] rpart_4.1-13 latticeExtra_0.6-28 stringi_1.2.4 RSQLite_2.1.1 genefilter_1.64.0
[56] checkmate_1.9.0 rlang_0.4.10 pkgconfig_2.0.2 bitops_1.0-6 lattice_0.20-35
[61] purrr_0.3.4 GenomicAlignments_1.18.1 htmlwidgets_1.3 bit_1.1-14 tidyselect_1.1.0
[66] plyr_1.8.4 magrittr_1.5 R6_2.3.0 generics_0.0.2 Hmisc_4.1-1
[71] DBI_1.0.0 pillar_1.5.1 foreign_0.8-70 withr_2.1.2 survival_2.42-3
[76] RCurl_1.95-4.11 nnet_7.3-12 tibble_3.1.0 crayon_1.3.4 utf8_1.1.4
[81] progress_1.2.0 locfit_1.5-9.1 grid_3.5.1 data.table_1.12.0 blob_1.1.1
[86] digest_0.6.18 xtable_1.8-3 tidyr_0.8.2 munsell_0.5.0
Mike, Sorry, I realized I was stupidity taking only the longer transcript. All is working now - apologies for the trouble!
Gaia