Hello there, I see that many of the other Non-Species RefSeq IDs are repetitive and blat to multiple locations. Your brief methods say that if an RNA aligned to multiple places, the highest identity was retrieved and alignments having a "base identity level within 0.5% of the best and 25% base identity with the genomic sequence were kept". Is there a table that displays how well each RNA aligned to a genome and its base identity with the same transcript aligning to other locations?
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