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No overlaps or Enrichment in Results #12
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Hi, |
I used hg19 assembly. setwd("/Users/uqsperiy/Brain_Data/") Or download other versionsremapCatalog2018hg19 <- downloadRemapCatalog(demo.dir, version = "2018", assembly = "hg19") |
The bed file chr1 52317230 52317231 |
hello, thanks you |
Here it is:
|
thank you for your response |
I did that and I am getting an error: |
I am using SNP data in regulatory regions to calculate enrichments. I am using the R package.
My Input data (hg38) looks like this:
GRanges object with 1800 ranges and 0 metadata columns:
seqnames ranges strand
[1] chr1 51851558-51851559 *
[2] chr1 51800569-51800570 *
[3] chr1 51825311-51825312 *
[4] chr1 51832478-51832479 *
[5] chr1 51845209-51845210 *
However, I am not getting any results.
TAL1 TAL1 0 0 0 NaN NA NA NA NA
GABPA GABPA 0 0 0 NaN NA NA NA NA
FOXP1 FOXP1 0 0 0 NaN NA NA NA NA
NME2 NME2 0 0 0 NaN NA NA NA NA
NRF1 NRF1 0 0 0 NaN NA NA NA NA
CTCF CTCF 0 0 0 NaN NA NA NA NA
e.significance e.value
TAL1 NA NA
GABPA NA NA
FOXP1 NA NA
NME2 NA NA
NRF1 NA NA
CTCF NA NA
I am not sure what I am doing wrong and would appreciate any feedback.
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