1) O'Roak, B. J., P. Deriziotis, et al. (2011). "Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations." Nat Genet 43(6): 585-589.
2) Yan, X. J., J. Xu, et al. (2011). "Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia." Nat Genet 43(4): 309-315.
*This pipeline (shown above) is a general representation and modification is necessary for specific project.