Can't merge snATAC samples
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Entering edit mode
11 months ago
myoui3122010 ▴ 30

I downloaded supplementary files from GSE232480 to get used to analyzing snATAC data.

filter_premerge <- function(fragment_path, count_path, meta_data_path, annotations) {
mouse_frag <- read.delim(fragment_path, header = TRUE, nrows = 10)

mouse_count <- Read10X_h5(count_path)

mouse_assay <- CreateChromatinAssay(
counts = mouse_count,
sep = c(":", "-"),
fragments = fragment_path,
min.cells = 10,
min.features = 200
)

mouse_meta <- read.csv(meta_data_path, header = TRUE, row.names = 1)

mouse_obj <- CreateSeuratObject(
counts = mouse_assay,
 = mouse_meta,
assay = 'ATAC'
)

Annotation(mouse_obj) <- annotations  

mouse_obj <- NucleosomeSignal(mouse_obj)
mouse_obj <- TSSEnrichment(mouse_obj)

mouse_obj$pct_reads_in_peaks <- mouse_obj$peak_region_fragments / mouse_obj$passed_filters * 100
mouse_obj$blacklist_ratio <- mouse_obj$blacklist_region_fragments / mouse_obj$peak_region_fragments

mouse_obj <- subset(
mouse_obj, 
subset = peak_region_fragments > 2000 & peak_region_fragments < 50000 & 
  pct_reads_in_peaks > 30 & blacklist_ratio < 0.05 &
  nucleosome_signal < 2 & TSS.enrichment > 2
)

return(mouse_obj)
}

Used this function to create seurat objects, for the next step I have to merge four such objects then further downstream analysis. But there is a problem with the merge, the ram gets exhausted and the kernel is restarted. enter image description here This is the output before the kernel restarts, I thought since I only have 32GB of memory that could be the issue.

So I used seurat IntegrateData method to see if that works, but that didn't work either and this time I still had 50% of memory left with the code running indefinitely. enter image description here

Finally I tried to use Harmony integration, now again stuck at scaleData. Runs Indefinitely. enter image description here

Any suggestions will be appreciated, Thanks

snATAC • 329 views
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