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I used hg19 for direct comparison. How should the coordinates in the configuration file be correctly derived? The regions that qMotif uses seems to be adjacent to the ones I get from Table Browser, but I don't understand what the difference is.
Also, the section which describes the XML file does not give an example of how to correctly interpret it. How should the user determine the telomere length from the various numbers in the XML file?
The text was updated successfully, but these errors were encountered:
It would be nice to know how to create the configuration for another genome, such as hg38 or mouse genome. The example is:
but, when I use UCSC Genome Browser's Table Browser and extract telomeres from the Gap table, I got different coordinates.
I used hg19 for direct comparison. How should the coordinates in the configuration file be correctly derived? The regions that qMotif uses seems to be adjacent to the ones I get from Table Browser, but I don't understand what the difference is.
Also, the section which describes the XML file does not give an example of how to correctly interpret it. How should the user determine the telomere length from the various numbers in the XML file?
The text was updated successfully, but these errors were encountered: