Open jcm6t opened 3 days ago
Hi,
build argument is only useful if you'd like to query UCSC for gene models. In your case, you should use a custom gtf file. Also set query_ucsc = FALSE
so that it wont try to connect to the UCSC.

t <- track_extract(colData = bigwigs, query_ucsc = FALSE, gtf=gtffile, gene = "Kirrel2")
Parsing gtf file.. Error in track_extract(colData = bigwigs, query_ucsc = FALSE, gtf = gtffile, : No transcript models found for Kirrel2
I have attached the gtf.
etbl = .parse_gtf(gtf = "kirrel2.gtf", genename = "Kirrel2") Parsing gtf file.. Warning message: In .parse_gtf(gtf = "kirrel2.gtf", genename = "Kirrel2") : Requested gene or transcript could not be found within the requested loci!
Which is a bit strange since the gtf is formatted correctly and parsed by trackplot.R and Kirrel2 is specified as a gene_name in the parsed info column. I thought you would be able to see the problem faster.
Thanks, Joe
On Jun 30, 2024, at 4:31 AM, Anand Mayakonda @.***> wrote:
Hi,
build argument is only useful if you'd like to query UCSC for gene models. In your case, you should use a custom gtf file. Also set query_ucsc = FALSE so that it wont try to connect to the UCSC.
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Hi,
The attachment is missing. Could you please tray again?
Here is the gtf. (it was rejected because not a recognized file type).
Is there a way to pass in a non-custom genome build in the read_coldata() step ? My reads are aligned to a specific mouse strain genome but it is not the standard mm build.
Thanks.