Hello everyone!
The problem of the day that has me a little stymied is the following:
I try to visualise a large alignment (bam file) in either IGV or tablet.
I have tried to upload the feature file (GFF3); to help me navigate. No luck.
My suspicion is; that the name of the contigs does not match between genome reference and gff.
My reference genome is a whole genome shotgut assembly consisting of a ton of scaffolds.
These are named as follows (example): gi|123456789|ref|NW_123456789.1|
They are also showing up in my bam file; so all good there!
The gff file, if I interpret it correctly; only uses the NW_123456789.1 part as the reference; which is why I assume tablet and IGV cannot recognize the features.
Now, the solution would be to create an alias file. But, how do I do it? I have 100.000 odd scaffolds; doing it by hand is out of the question...
The problem of the day that has me a little stymied is the following:
I try to visualise a large alignment (bam file) in either IGV or tablet.
I have tried to upload the feature file (GFF3); to help me navigate. No luck.
My suspicion is; that the name of the contigs does not match between genome reference and gff.
My reference genome is a whole genome shotgut assembly consisting of a ton of scaffolds.
These are named as follows (example): gi|123456789|ref|NW_123456789.1|
They are also showing up in my bam file; so all good there!
The gff file, if I interpret it correctly; only uses the NW_123456789.1 part as the reference; which is why I assume tablet and IGV cannot recognize the features.
Now, the solution would be to create an alias file. But, how do I do it? I have 100.000 odd scaffolds; doing it by hand is out of the question...
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