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License: GNU General Public License v3.0
An accurate, robust, and fast genotype caller for bisulfite-sequencing data
License: GNU General Public License v3.0
Hi,
I am analyzing methylation data- finding differentially methylated sites/regions, and I wanted to inquire about suggestions whether my input is good or if I should preprocess with better software.
My collaborator enzyme-converted DNA with the NEBNext® Enzymatic Methyl-seq Kit](https://www.neb.com/en-us/products/e7120-nebnext-enzymatic-methyl-seq-kit, and sequenced with Nova-seq. I removed adapters with trimgalore!, and then mapped the reads with bwa-meth, bam converted and sorted, and then used Picard to eliminate duplicate reads.
According to two papers, the bayesian model of cgmaptools is the suggested tool for non-model organisms. Hence I used the sorted-duplicate-removed bam files and generated the ATCGmap files and did the variant calling. My surprise was that the vcf file had degenerated bases.
Thus, I wanted first to ask if the sorted-deduplicated bam files could be used as input or if I should use the ATCGmap generated from them.
Thanks;
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