-
Notifications
You must be signed in to change notification settings - Fork 100
Description
Currently, if I am not mistaken, GeneActivity() uses as forced default gene_name column from the genome annotation of chromatin assay as basis for gene nomenclature. This then causes problems with label transfer from scRNA if scRNA has been processed with Ensembl ids. Could there be option in in GeneActivity which specifies the column used as gene identification. Like in this case:
GRanges object with 1763965 ranges and 5 metadata columns:
seqnames ranges strand | tx_id gene_name gene_id gene_biotype type
|
ENSMUSE00001236884 chr3 3508030-3508332 + | ENSMUST00000108393 Hnf4g ENSMUSG00000017688 protein_coding exon
ENSMUSE00000676606 chr3 3634150-3634347 + | ENSMUST00000108394 Hnf4g ENSMUSG00000017688 protein_coding exon
ENSMUSE00001345708 chr3 3638059-3638230 + | ENSMUST00000108393 Hnf4g ENSMUSG00000017688 protein_coding exon
There is ENSMUSG id available in the same annotation data.