--- title: "methods section" editor: visual format: html: code-fold: true code-summary: "Show the code" --- ::: callout-important This is draft method for Subproject "A" Nutrient exposure experiment - P verrocosa genome ::: ::: callout-warning I have some concern about quality of genome ::: ### DNA Methylation Analysis Deduplicated Alignment files (BAMs) were downloaded [from Becker](https://gannet.fish.washington.edu/Atumefaciens/hputnam-Becker_E5/WGBS_Becker_E5/Becker_WGBS/bismark_deduplicated/) Methylation levels were extracted ${bismark_dir}/bismark_methylation_extractor \ --bedGraph --counts --scaffolds \ --multicore 28 \ --counts \ --comprehensive \ --merge_non_CpG \ --buffer_size 75% \ *deduplicated.bam This was followed by coverage file generation find *deduplicated.bismark.cov.gz \ | xargs basename -s _R1_001_val_1_bismark_bt2_pe.deduplicated.bismark.cov.gz \ | xargs -I{} ${bismark_dir}/coverage2cytosine \ --genome_folder ${genome_folder} \ -o {} \ --merge_CpG \ --zero_based \ {}_R1_001_val_1_bismark_bt2_pe.deduplicated.bismark.cov.gz and files generated for downstream analysis.