Read counting against annotated features:

Question

ASpli: Error in h(simpleError(msg, call)) : error in evaluating the argument 'x' in selecting a method for function 'sort': 'start' or 'end' cannot contain NAs

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thithusuong.nguyen • 0

@f6f89172

Last seen 2.2 years ago

Australia

Dear ASpli maintainer team/users!

I was wondering if you could help me with an issue I have encountered when running jCounts. I got the error message as shown in the title and below. I've looked into "gbcounts@junction.counts" and I think the error was due to 325,589 rows that do not contain "gene_coordinates" information (shown as "-" instead of coordinate information). I wanted to filter out these rows and run jCounts again on the remaining rows (550,301 rows) but so far have been unsuccessful. I've tried to subset "gbcounts@junction.counts" by running subset(gbcounts@junction.counts, gene_coordinates != "-") but it only worked on the dataframe. I was thinking to somehow add this new "gbcounts@junction.counts" back into the gbcounts object but don't know how. I would appreciate it very much if anyone can give me some guidance on this.

Best regards,

Suong

```BiocManager::install("ASpli")

```library(ASpli)

```library(GenomicFeatures)

```gtfFileName <- "/home/suong/Documents/Effluxer project/novel_transcripts/ASpli_R_Oct2022/Pvulgaris_442_v2.1.gene_exons.gff3"

```genomeTxDb <- makeTxDbFromGFF( gtfFileName )

```features <- binGenome( genomeTxDb )

```geneCoord <- featuresg( features )

```binCoord <- featuresb( features )

```junctionCoord <- featuresj( features )

```BAMFiles <- c("/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_16DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_16DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_16DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_16DPA_4_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_21DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_21DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_21DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_21DPA_4_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_26DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_26DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_26DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/EM_26DPA_4_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_16DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_16DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_16DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_16DPA_4_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_21DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_21DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_21DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_21DPA_4_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_26DPA_1_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_26DPA_2_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_26DPA_3_valAligned.sortedByCoord.out.bam", "/home/suong/Documents/Effluxer project/novel_transcripts/bam_bai/SC_26DPA_4_valAligned.sortedByCoord.out.bam")

```(targets <- data.frame( bam = BAMFiles, tissue = c( 'Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo','Embryo', 'Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat','Seedcoat'), time = c( '16DPA', '16DPA', '16DPA', '16DPA', '21DPA', '21DPA', '21DPA', '21DPA', '26DPA', '26DPA', '26DPA', '26DPA', '16DPA', '16DPA', '16DPA', '16DPA', '21DPA', '21DPA', '21DPA', '21DPA', '26DPA', '26DPA', '26DPA', '26DPA'), stringsAsFactors = FALSE ))

```getConditions( targets )

```mBAMs <- data.frame(bam = sub("_[1_2_3_4_]","",targets$bam[c(1,5,9,13,17,21)]), condition= c("Embryo_16DPA","Embryo_21DPA","Embryo_26DPA", "Seedcoat_16DPA", "Seedcoat_21DPA", "Seedcoat_26DPA"))

Read counting against annotated features:

```gbcounts <- gbCounts(features=features, targets=targets, minReadLength = 100, maxISize = 50000)

```gbcounts

Junction-based de-novo counting and splicing signal estimation:

```asd <- jCounts(counts=gbcounts, features=features, minReadLength=100)

```asd

My error output

```asd <- jCounts(counts=gbcounts, features=features, minReadLength=100)

Error in h(simpleError(msg, call)) : error in evaluating the argument 'x' in selecting a method for function 'sort': 'start' or 'end' cannot contain NAs

In addition: Warning messages:

1: In matrix(unlist(strsplit(jnames, "[.]")), byrow = TRUE, ncol = 3) : data length [1646215] is not a sub-multiple or multiple of the number of rows [548739]

2: In .createGRangesExpJunctions(junctionNames) : NAs introduced by coercion

Here is my junction.counts data

head(gbcounts@junction.counts)

sessionInfo( )

```sessionInfo( )

R version 4.2.1 (2022-06-23) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Linux Mint 20.1

Matrix products: default BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.9.0 LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.9.0

locale: 1 LC_CTYPE=en_AU.UTF-8 LC_NUMERIC=C LC_TIME=en_AU.UTF-8 LC_COLLATE=en_AU.UTF-8 LC_MONETARY=en_AU.UTF-8
[6] LC_MESSAGES=en_AU.UTF-8 LC_PAPER=en_AU.UTF-8 LC_NAME=C LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_AU.UTF-8 LC_IDENTIFICATION=C

attached base packages: 1 stats4 parallel stats graphics grDevices utils datasets methods base

other attached packages: 1 dplyr_1.0.10 GenomicFeatures_1.48.4 GenomicRanges_1.48.0 GenomeInfoDb_1.32.4 ASpli_2.6.0 AnnotationDbi_1.58.0
[7] IRanges_2.30.1 S4Vectors_0.34.0 Biobase_2.56.0 BiocGenerics_0.42.0 edgeR_3.38.4 limma_3.52.4

loaded via a 1 colorspace_2.0-3 deldir_1.0-6 rjson_0.2.21 ellipsis_0.3.2 htmlTable_2.4.1
XVector_0.36.0 base64enc_0.1-3 dichromat_2.0-0.1 rstudioapi_0.14
bit64_4.0.5 fansi_1.0.3 xml2_1.3.3 codetools_0.2-18
cachem_1.0.6 knitr_1.40 Formula_1.2-4 Rsamtools_2.12.0
dbplyr_2.2.1 png_0.1-7 BiocManager_1.30.18 compiler_4.2.1
backports_1.4.1 lazyeval_0.2.2 assertthat_0.2.1 Matrix_1.5-1
cli_3.4.1 htmltools_0.5.3 prettyunits_1.1.1 tools_4.2.1
gtable_0.3.1 glue_1.6.2 GenomeInfoDbData_1.2.8 rappdirs_0.3.3
vctrs_0.4.2 Biostrings_2.64.1 rtracklayer_1.56.1 xfun_0.33
lifecycle_1.0.3 ensembldb_2.20.2 restfulr_0.0.15 statmod_1.4.37
zlibbioc_1.42.0 MASS_7.3-58 scales_1.2.1 BiocStyle_2.24.0
VariantAnnotation_1.42.1 ProtGenerics_1.28.0 hms_1.1.2 MatrixGenerics_1.8.1
AnnotationFilter_1.20.0 RColorBrewer_1.1-3 yaml_2.3.5 curl_4.3.3
gridExtra_2.3 ggplot2_3.3.6 UpSetR_1.4.0 rpart_4.1.16
latticeExtra_0.6-30 stringi_1.7.8 RSQLite_2.2.18 BiocIO_1.6.0
filelock_1.0.2 BiocParallel_1.30.3 rlang_1.0.6 pkgconfig_2.0.3
bitops_1.0-7 evaluate_0.17 lattice_0.20-45 purrr_0.3.5
GenomicAlignments_1.32.1 cowplot_1.1.1 bit_4.0.4 tidyselect_1.2.0
magrittr_2.0.3 R6_2.5.1 generics_0.1.3 Hmisc_4.7-1
DBI_1.1.3 foreign_0.8-82 pillar_1.8.1 nnet_7.3-17
KEGGREST_1.36.3 RCurl_1.98-1.9 tibble_3.1.8 crayon_1.5.2
utf8_1.2.2 BiocFileCache_2.4.0 rmarkdown_2.17 jpeg_0.1-9
locfit_1.5-9.6 grid_4.2.1 data.table_1.14.2 blob_1.2.3
pbmcapply_1.5.1 tidyr_1.2.1 munsell_0.5.0 Gviz_1.40.1

ASpli • 4.5k views

ADD COMMENT • link updated 15 months ago by andresrabinovich • 0 • written 2.2 years ago by thithusuong.nguyen • 0

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Hey there! I was having this exact problem and that same error. I had no clue what could be going wrong because it only showed up with specific BAM files and not with others. I ended up realizing that when I used TrimGalore (for removing low quality reads and adapters) sometimes this error showed up, but if I processed the same library with Trimmomatic the error disappeared. That's how I got my way around the problem (nowhere near actually solving it hahaha, but enough for me to move on). Regards!

ADD REPLY • link 24 months ago Jesús M • 0

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Entering edit mode

Hello, I am late to the party, but I had the same issue, with some datasets, and I solved adding the following line of code:

gbcounts@junction.counts<-na.omit(gbcounts@junction.counts)

Example:

# Read counting against annotated features
gbcounts <- gbCounts(
  features = features,
  targets = targets,
  minReadLength = 100,
  maxISize = 50000,
  strandMode = 2,
  libType = "PE"
)
# Export splicing junction counts
writeCounts(counts = gbcounts,
            output.dir = paste0("gbCounts", fileName))
gbcounts@junction.counts<-na.omit(gbcounts@junction.counts)
# Junction-based de-novo counting and splicing signal estimation
asd <- jCounts(
  counts = gbcounts,
  features = features,
  minReadLength = 100,
  libType = "PE",
  strandMode = 2
)

Cheerio, M

ADD REPLY • link 15 months ago MT ▴ 10

0

Entering edit mode

Problem might have been solved in devel version 2.11.1 (https://www.bioconductor.org/packages/devel/bioc/html/ASpli.html)

ADD REPLY • link 15 months ago andresrabinovich • 0