You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
I use the tombo detect_modifications alternative_model to dectect the RNA m5C modification. Then I use the tombo text_output browser_files to get the resluts.
I get fraction_modified_reads.minus.wig and fraction_modified_reads.plus.wig two files. I think one file is for fwd_strand while another is for rev_strand.
Because my data is RNA and my reference sequence is synthetic sequence or transcriptome. So in this case, which one should I use in fraction_modified_reads.minus.wig and fraction_modified_reads.plus.wig ?
I think the raw file in fast5 is form 3' to 5' (RNA is currently sequenced in the 3’ to 5’ direction). So in RNA sequencing, why here have two files for plus strand and minus strand?
Thanks!
The text was updated successfully, but these errors were encountered:
guangzhaocs
changed the title
Which strand to use in RNA modification
Which strand to use in RNA modification?
May 24, 2024
Hi,
I use the
tombo detect_modifications alternative_model
to dectect the RNA m5C modification. Then I use thetombo text_output browser_files
to get the resluts.I get
fraction_modified_reads.minus.wig
andfraction_modified_reads.plus.wig
two files. I think one file is forfwd_strand
while another is forrev_strand
.Because my data is RNA and my reference sequence is synthetic sequence or transcriptome. So in this case, which one should I use in
fraction_modified_reads.minus.wig
andfraction_modified_reads.plus.wig
?I think the raw file in fast5 is form 3' to 5' (RNA is currently sequenced in the 3’ to 5’ direction). So in RNA sequencing, why here have two files for plus strand and minus strand?
Thanks!
The text was updated successfully, but these errors were encountered: