Open Derryxu opened 2 years ago
Dear Xu,
I'm really sorry that it has taken me this long to get back to you on this. I recently had to redo this analysis and couldn't exactly replicate the process used in the paper either, so I came up with a close approximation based on the description in the methods section of the nanocompore paper. You can follow the instructions on which references I used and on how to generate the m6A peaks file that I did in the github repository for NanOlympicsMod linked below.
https://github.com/mfurla/NanOlympicsMod/tree/main/Scripts
Look over these two files if you still need to replicate the work.
m6A_peaks_yeast_SK1_liftover.pdf convert_m6a_to_sk1.py
Again, sorry for the 1 year delay in getting back to you, and I hope that this information is still useful to your work after all this time.
All the best, Logan
Hi, I hava two problem in learning nanocompore.
The following files are provided in https://www.yeastgenome.org/strain/SK1 about reference file site mentioned in paper. Is the
SK1_NCSL00000000_SGD_rna_genomic.fsa
correct file for alignment ? Could you guide me on which Yeast SK1 transcriptome reference file to use for direct yeast RNA ?In addition, Nanocompare compiled an orthogonal reference set of m6A sites from SK1 yeast by taking m6ASeq sites from Schwartz et al. and
MAZTER-seq
sites from Garcia-Camposet al. for benchmarking results against known yeast m6A sites. Is it possible to detail the processing of 1297 reference m6A positions? I was unable to successfully reproduce as I can't find the sites file of MAZTER-seq clearly. Could the ground-truth m6a sites set file be shared please? Is there any way can obtain it?Thanks very much! Best, xu