1.Trimmed the adaptors in the fastq files using TrimGalore!
./trim_galore -a <adapter> --gzip --rrbs --length 15 --stringency 4 FILE
2.Mapped to the baboon reference genome using BSseeker2
python bs_seeker2-align.py -i FILE.fq --aligner=bowtie2 -o FILE.bam -g reference.fa -r
python bs_seeker2-call_methylation.py -i FILE.bam -o FILE --db reference
3.Called SNPs using CGmaptools with the BayesWC strategy
cgmaptools snv -i FILE.ATCGmap.gz -m bayes -v FILE.vcf -o FILE.snv –bayes-e=0.01 –bayes-dynamicP -a
4.Merged and filtered VCF files using VCFtools
vcftools --vcf FILE.vcf –minDP 3 --max-missing 0.5 --maf 0.05 --recode --recode-INFO-all --out FILE
5.Called allele-specific methylation using CGmaptools
cgmaptools asm -r reference.fa -b FILE.bam -l FILE.vcf > FILE.asm
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