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Hi, there
The scallop2 is a good software to do the assembly of the RNA-seq data. These day, I also check the results form the scallop with the IGV. There are some transcripts that merge from two seperate transcripts, and the other part was labeled as UTR region. As shown in the following picture, the transcripts from gene TGS101 and UEVLD covered each other. I wonder the reality of these transcripts and how to deal with? Any ideas?
Thank so much!
yizhong Huang
The text was updated successfully, but these errors were encountered:
Hi, there
The scallop2 is a good software to do the assembly of the RNA-seq data. These day, I also check the results form the scallop with the IGV. There are some transcripts that merge from two seperate transcripts, and the other part was labeled as UTR region. As shown in the following picture, the transcripts from gene TGS101 and UEVLD covered each other. I wonder the reality of these transcripts and how to deal with? Any ideas?
Thank so much!
yizhong Huang
The text was updated successfully, but these errors were encountered: