Samuel G. Younkin

According to our database, Samuel G. Younkin authored at least 3 papers between 2012 and 2016.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2016

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

2014

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

2012

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