Fast detection of de novo copy number variants from SNP arrays for case-parent trios. - Robert B. Scharpf; Terri H. Beaty; Holger Schwender; Samuel G. Younkin; Alan F. Scott; Ingo Ruczinski (BMC Bioinform., 2012)

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. - Alexandre Bureau; Samuel G. Younkin; Margaret M. Parker; Joan E. Bailey-Wilson; Mary L. Marazita; Jeffrey C. Murray; Elisabeth Mangold; Hasan Albacha-Hejazi; Terri H. Beaty; Ingo Ruczinski (Bioinform., 2014)

Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection. - Qi Zhang; Xin Zeng; Samuel G. Younkin; Trupti Kawli; Michael P. Snyder; Sündüz Keles (BMC Bioinform., 2016)