tximport error: vroom
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RLiu ▴ 40
@7cbf87e1
Last seen 12 months ago
Canada

I'm trying to import a list of salmon counts files quant.sf:

txi <- tximport(files=files, type="salmon", tx2gene=tx2gene[,c("refseq", "entrezid")], countsFromAbundance="lengthScaledTPM")

Rstudio threw me an error:

reading in files with read_tsv
1 Error in vroom_(file, delim = delim %||% col_types$delim, col_names = col_names,  : 
  bad value

why did it happen?

Here are what files and tx2gene look like:

> head(files)
                                                       cy201702 
"/Users/maxineliu/work/bufo/RNA/salmon/cy201702_quant/quant.sf" 
                                                       cy201802 
"/Users/maxineliu/work/bufo/RNA/salmon/cy201802_quant/quant.sf" 
                                                       cy201902 
"/Users/maxineliu/work/bufo/RNA/salmon/cy201902_quant/quant.sf" 
                                                       cy202302 
"/Users/maxineliu/work/bufo/RNA/salmon/cy202302_quant/quant.sf" 
                                                       cy202402 
"/Users/maxineliu/work/bufo/RNA/salmon/cy202402_quant/quant.sf" 
                                                       cy202502 
"/Users/maxineliu/work/bufo/RNA/salmon/cy202502_quant/quant.sf"
head(tx2gene[,c("refseq", "entrezid")])
          refseq  entrezid
1 XM_044268240.1 122946843
2 XM_044268241.1 122919300
3 XM_044268242.1 122919300
4 XM_044268243.1 122919300
5 XM_044268244.1 122919301
6 XM_044268245.1 122919299
tximport • 2.6k views
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@mikelove
Last seen 4 hours ago
United States

Check that they all have same number of lines. I guess one of them was interrupted while writing out and may need to be re-run (Salmon).

Seems an issue with readr (see below). Try importer=read.delim

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I checked that all quant.sfs have the same line number (42013 lines in each file), which is different from tx2gene (81493 lines).

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I also ran into this same issue today. All my quant.sf files are the same length, were generated within the last month, do not contain comments at the beginning (see the cross-post's suggestion), and worked with tximport until today (I've used the same script for the past three weeks).

My tx2gene is 34403 rows long. All of my quant.sf files are 32262 rows long.

I think this is due to an issue with vroom. My old script was on vroom_1.6.3. I updated today from vroom_1.6.3 to vroom_1.6.4 and this issue began afterwards. I believe this is the reason since readr which also depends on vroom gives me the same error, while data.table::fread (doesn't depend on vroom) does not throw an error.

> # Use readr
> data <- readr::read_delim("path/quant.sf", "\t")
  Error in vroom_(file, delim = delim %||% col_types$delim, col_names = col_names,  :                                                                                                                         
  bad value

> # Use fread from data.table
> data <- data.table::fread("path/quant.sf")

I've tried to downgrade back to vroom_1.6.3, but I still get the same error, so I might be totally wrong that it is vroom's fault or something else might be going wrong I'm not sure how to fix.

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Thank you for providing this clue. I never installed vroom manually. I guess it is one of dependences for tximport that automatically installed in R.

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Of course! Let me know if you figure it out.

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You can force the function used for importing:

https://github.com/thelovelab/tximport/blob/devel/R/tximport.R#L265

Try importer=read.delim

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Worked perfectly! Thanks!

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yes! worked perfectly! Thank you~

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Hi Mike - I'm having the same issue with tximeta. Would you mind posting a how-to for how to edit the function in RStudio? thx.

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genes_results = tximport(files, type = 'rsem', txIn = F, txOut = F, ignoreTxVersion = TRUE, importer = read.delim)

you can change the type to whatever you used to align. I hope this helps.

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