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I have a simulated dataset, with a chromosome which contains a "perfect palindrome", which means the reverse complement is directly downstream to the primary sequence without intervening nucleotides.
Strangely, Sibelia, be it with -s loose or -s fine doesn't detect it. However, if I copy that palindrome sequence and ask Sibelia to search for syntheny between it and the chromosome it's copied from, then the palindrome is reported.
I can easily provide the file if needed.
Thanks a lot
The text was updated successfully, but these errors were encountered:
Other parts of the graph interferring with the part of the genomes you are interested in. It may hinder the bubble collapsing algorithm or something else
Hello,
I have a simulated dataset, with a chromosome which contains a "perfect palindrome", which means the reverse complement is directly downstream to the primary sequence without intervening nucleotides.
Strangely, Sibelia, be it with -s loose or -s fine doesn't detect it. However, if I copy that palindrome sequence and ask Sibelia to search for syntheny between it and the chromosome it's copied from, then the palindrome is reported.
I can easily provide the file if needed.
Thanks a lot
The text was updated successfully, but these errors were encountered: