Hello everyone,
I am using modkit to analyse the results from Dorado m6A_DRACH methylation base-calling.
(1) I have generated the bedmethyl file from bam file. Now i need a filter criteria for "coverage" and "mod_rate" to get rid of noisy predictions.
Can we directly use the filter on column "Nvalid_cov" as >=20 reads? or do we need to normalise it for per million reads?
(2) for Differential methylation analysis between conditions i am using dmr pair, following command
modkit dmr pair -a c6_r1.bed.gz -a c6_r2.bed.gz -a c6_r3.bed.gz -b dr6_r1.bed.gz -b dr6_r2.bed.gz -b dr6_r3.bed.gz -o dmr_result --ref Genome.fa --base A --threads 96 --log-filepath dmr_result.log
- How does modkit make the unified list of sites from both conditions with replicates?
- How does modkit tools handle the sites which are present in one condition and not in another?
- What kind of test modkit applies to get the DMR sites?
Thanks
Looks like you already opened an issue on
modkit
GitHub. That is probably the best place to ask this: https://github.com/nanoporetech/modkit/issues/364If you get an answer there please come back to this thread and post it here.