William Salerno, Ph.D.

Assistant Professor, Department of Molecular and Human Genetics

Contact information

william.salerno@bcm.edu

Publications

Beecham GW, Bis JC, Martin ER, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurol Genet. 2017;3(5):e194. doi:10.1212/NXG.0000000000000194.

Hampton OA, English AC, Wang M, et al. SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads. BMC Genomics. 2017;18(Suppl 6):691. doi:10.1186/s12864-017-4021-y.

Brody JA, Morrison AC, Bis JC, et al. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology. Nat Genet. 2017;49(11):1560-1563. doi:10.1038/ng.3968.

Xue C, Raveendran M, R Harris A, et al. The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences. Genome Res. 2016;26(12):1651-1662. doi:10.1101/gr.204255.116.

English AC, Salerno WJ, Hampton OA, et al. Assessing structural variation in a personal genome-towards a human reference diploid genome. BMC Genomics. 2015;16:286. doi:10.1186/s12864-015-1479-3.

English AC, Salerno WJ, Reid JG. PBHoney: identifying genomic variants via long-read discordance and interrupted mapping. BMC Bioinformatics. 2014;15:180. doi:10.1186/1471-2105-15-180.

Reid JG, Carroll A, Veeraraghavan N, et al. Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline. BMC Bioinformatics. 2014;15:30. doi:10.1186/1471-2105-15-30.

Salerno WJ, Havlak P, Miller J. Scale-invariant structure of strongly conserved sequence in genomic intersections and alignments. Proc Natl Acad Sci U S A. 2006;103(35):13121-5. doi:10.1073/pnas.0605735103.