I am currently using cDNA sequencing data, and when I tried to upload reads on ucsc, I found my reads representing the strand information in opposite way (I am very postive that all of the sequeces are showing the opposite direction). I am wondering if there's any specific options or steps needed to process the data.
I have generated my data straight out from the MINion, mapped using minimap2 without any filteirng. So I am wondering if there any filtering steps that you perform that is necessary for nanopore sequencing analysis? I was doing some research as well, but I am also hoping to get methods that you might be using.
Hello.
I am currently using cDNA sequencing data, and when I tried to upload reads on ucsc, I found my reads representing the strand information in opposite way (I am very postive that all of the sequeces are showing the opposite direction). I am wondering if there's any specific options or steps needed to process the data.
I have generated my data straight out from the MINion, mapped using minimap2 without any filteirng. So I am wondering if there any filtering steps that you perform that is necessary for nanopore sequencing analysis? I was doing some research as well, but I am also hoping to get methods that you might be using.
Thank you for your time and generous help.