SNP calling I – alignment programs and PCR duplicates

I have tested various SNP calling methods using exome re-sequencing data from 12 interior spruce samples. I tried Bowtie2, BWA (mem), Picard (mark duplicates) and GATK for indel realignment and base quality recalibration. For SNP calling I used mpileup with and without BAQ as well as the Unified Genotyper from GATK. For an interesting and informative workshop outlining the Broad best practices SNP calling pipeline check out these youtube videos ( My results are in a series of blog posts and I hope you find them useful. Please let me know if you have any suggestions for SNP calling. We only want to do the alignments and SNP calling once for the entire set of samples, because it is going to take a long time!

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