I am running bwameth.py tabulate on an Ecoli bisulfite treated sample aligned with bismark/bowtie2.
I was getting no methylation calls with the default parameters, so I changed to --context all and ran a parameter sweep on the --map-q option. If I run this on the first 1000bp of the Ecoli genome, I get no calls for mapq values ranging from 60-43, but then I get 138 lines in the meth.vcf file from map-q 42 downwards.
Any ideas what would be a good way of running bwameth/BisSNP on Ecoli data like this?
I read a paper that says Ecoli methylation is found in around 1-2 cases every 1000bp for the CmCWGG motif, but I am unsure how to specify that in BisSNP. Is it possible?
I think it's better to use something like PileOMeth or maybe biscuit if you have trouble with tabulate_methlation since it's just a thin wrapper around BisSNP.
Hi,
I am running
bwameth.py tabulate
on an Ecoli bisulfite treated sample aligned with bismark/bowtie2.I was getting no methylation calls with the default parameters, so I changed to
--context all
and ran a parameter sweep on the--map-q
option. If I run this on the first 1000bp of the Ecoli genome, I get no calls for mapq values ranging from 60-43, but then I get 138 lines in the meth.vcf file from map-q 42 downwards.Any ideas what would be a good way of running bwameth/BisSNP on Ecoli data like this?
I read a paper that says Ecoli methylation is found in around 1-2 cases every 1000bp for the CmCWGG motif, but I am unsure how to specify that in BisSNP. Is it possible?