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You need to use the
No, if you want to run LinkPeaks() there's no need to run Cicero |
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Full code as in from the very start of analysis? |
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Hi Tim,
I was trying to generate a cds object with a view to getting the co-accessible sites. I'm getting the following error:
int.cds <- as.CellDataSet(integrated,assay="ATAC", reduction = "wnn.umap")
Error in validObject(.Object) :
invalid class "CellDataSet" object: sampleNames differ between assayData and phenoData
In addition: Warning messages:
1: In .sparse2dense(e1) :
sparse->dense coercion: allocating vector of size 24.5 GiB
2: In .sparse2dense(e2) :
sparse->dense coercion: allocating vector of size 24.5 GiB
What follows are the specifics of my object:
An object of class Seurat
218108 features across 20983 samples within 4 assays
Active assay: ATAC (156711 features, 156711 variable features)
2 layers present: counts, data
3 other assays present: RNA, SCT, integrated
5 dimensional reductions calculated: pca, umap.rna, lsi, umap.atac, wnn.umap
> integrated@reductions
$pca
A dimensional reduction object with key PC_
Number of dimensions: 50
Number of cells: 20983
Projected dimensional reduction calculated: FALSE
Jackstraw run: FALSE
Computed using assay: integrated
$umap.rna
A dimensional reduction object with key rnaUMAP_
Number of dimensions: 2
Number of cells: 20983
Projected dimensional reduction calculated: FALSE
Jackstraw run: FALSE
Computed using assay: integrated
$lsi
A dimensional reduction object with key LSI_
Number of dimensions: 50
Number of cells: 20983
Projected dimensional reduction calculated: FALSE
Jackstraw run: FALSE
Computed using assay: ATAC
$umap.atac
A dimensional reduction object with key atacUMAP_
Number of dimensions: 2
Number of cells: 20983
Projected dimensional reduction calculated: FALSE
Jackstraw run: FALSE
Computed using assay: ATAC
$wnn.umap
A dimensional reduction object with key wnnUMAP_
Number of dimensions: 2
Number of cells: 20983
Projected dimensional reduction calculated: FALSE
Jackstraw run: FALSE
Computed using assay: ATAC
I integrated the RNA modality from 3 multiome assays but NOT the ATAC modalities since these were multiome datasets.. So there is overlap when I look at the wnn.umap projection and umap.rna projection but NOT with the umap.atac projection.
Is that to be expected? Also to run LinkPeaks() I do have to establish the conns correct?
So which reduction should I be using? wnn.umap or umap.atac.
What is the error:
invalid class "CellDataSet" object: sampleNames differ between assayData and phenoData referring to? How may I fix it?
Despite adding the chr prefix to the ranges in the ATAC component of the object I'm still unable to run the Motif analysis. As a reminder I'm using the Macaca mulatta datasets and used the gtf file at Ensembl for Mmul_10 for annotation purposes.
Thanks for your time!
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