Hi,
I have used tophat to run rna-seq against to ref_genome without annotation,and it output indel discovery,insertion.bed and deletion.bed.
My question is how do I pick out high significant mutation from *.bed .
Thanks
Best Regard!
I have used tophat to run rna-seq against to ref_genome without annotation,and it output indel discovery,insertion.bed and deletion.bed.
My question is how do I pick out high significant mutation from *.bed .
Thanks
Best Regard!