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One error when I loading data by using SoupX, Thank you so much. #8

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MQMQ2018 opened this issue Jan 15, 2019 · 5 comments
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@MQMQ2018
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Dear Dr. Matthew Young,

It is nice to try to reduce the ambient mRNA in scRNA-seq analysis. I tried to read my 10xgenomics scRNAseq data as below, but encountered an error as below, could you please help to check and give me some tips? Is that because of I loading the folder of aggregated samples by using Cellranger -aggr? Thank you so much.

#===#

dataDirs=c("/scRNAseq/BeforeForceCell/Mixtured/outs")
scl = load10X(dataDirs)
Loading data for 10X channel Channel1 from /scRNAseq/BeforeForceCell/Mixtured/outs
Error in intI(j, n = x@Dim[2], dn[[2]], give.dn = FALSE) :
'NA' indices are not (yet?) supported for sparse Matrices

#===#

Best,
Qi

@shristi-shrestha
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I have the same problem. Did you figure out the fix?

@MQMQ2018
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MQMQ2018 commented Feb 28, 2019 via email

@JonathanCruard
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Hi, I have that problem too, got some clues to resolve this?
Thanks,
JC

@constantAmateur
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This error usually indicates a duplicate or NA row or column name in the sparse matrix. If you have checked your data and are confident this is not the case, please send me an example file and I will investigate further.

@JonathanCruard
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Just saw that you fixed the problem of loading aggregated datasets from cellranger.
By the way thank you for that!
But I noticed that it keep the aggregated samples in the same soup channel. Wouldn't it be better if those aggregated samples were splited into different channels?
Best,
JonathanCruard

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