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hello,Professor
I have two genome from two species and two set of hic reads from two genomes. I want to identify SVs between two genomes from two species by hic reads. I am confused whether should I align B genome hic reads to A reference genome to generate the input cool file of EagleC?
Could you give me any suggestions?
Looking forward with your reply!
The text was updated successfully, but these errors were encountered:
Hi, thanks for your interest ... but EagleC was not designed for identifying SVs between genomes of two species. Actually, since the sequences of the two genomes are known, I think the most straightforward way for your task is to align the two genomes using a traditional sequence alignment software :)
hello,Professor
I have two genome from two species and two set of hic reads from two genomes. I want to identify SVs between two genomes from two species by hic reads. I am confused whether should I align B genome hic reads to A reference genome to generate the input cool file of EagleC?
Could you give me any suggestions?
Looking forward with your reply!
The text was updated successfully, but these errors were encountered: