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For two isoforms to be compared at the sequence level, they should overlap at the exonic level by a certain percent (eg, each exon should be 90% overlapping)
If they are missing an entire exon or something like that, I suggest that is better reported as a splice variant. We aren't calling variants -- we're finding (significant) differences
The text was updated successfully, but these errors were encountered:
For two isoforms to be compared at the sequence level, they should overlap at the exonic level by a certain percent (eg, each exon should be 90% overlapping)
If they are missing an entire exon or something like that, I suggest that is better reported as a splice variant. We aren't calling variants -- we're finding (significant) differences
The text was updated successfully, but these errors were encountered: