Hi, All,
I would like to use the raw genome pair-end data or the assembled scaffold and RAD sequencing data to detect inversion and the breaking point for special region in the genome and special chromosome. I heard that using pair-end data can deal with these questions, but I do not have much experience on it... Could anyone give me any suggestion?
Thanks in advance!
All the best,
Sadiexiaoyu
I would like to use the raw genome pair-end data or the assembled scaffold and RAD sequencing data to detect inversion and the breaking point for special region in the genome and special chromosome. I heard that using pair-end data can deal with these questions, but I do not have much experience on it... Could anyone give me any suggestion?
Thanks in advance!
All the best,
Sadiexiaoyu
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