Robert B. Scharpf

According to our database, Robert B. Scharpf authored at least 8 papers between 2007 and 2022.

Collaborative distances:

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

2022

Estimation of cancer cell fractions and clone trees from multi-region sequencing of tumors.

Lily Zheng, Noushin Niknafs, Laura D. Wood, Rachel Karchin, Robert B. Scharpf

Bioinform., 2022

Detecting and quantifying antibody reactivity in PhIP-Seq data with BEER.

Athena Chen, Kai Kammers, H. Benjamin Larman, Robert B. Scharpf, Ingo Ruczinski

Bioinform., 2022

2019

Detection of rare disease variants in extended pedigrees using RVS.

Thomas Sherman, Jack M. Fu, Robert B. Scharpf, Alexandre Bureau, Ingo Ruczinski

Bioinform., 2019

Detection of de novo copy number deletions from targeted sequencing of trios.

Jack M. Fu, Elizabeth J. Leslie, Alan F. Scott, Jeffrey C. Murray, Mary L. Marazita, Terri H. Beaty, Robert B. Scharpf, Ingo Ruczinski

Bioinform., 2019

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

2011

Performance assessment of copy number microarray platforms using a spike-in experiment.

Eitan Halper-Stromberg, Laurence Frelin, Ingo Ruczinski, Robert B. Scharpf, Chunfa Jie, Benilton S. Carvalho, Haiping Hao, Kurt N. Hetrick, Anne Jedlicka, Amanda Dziedzic, Kim Doheny, Alan F. Scott, Steve Baylin, Jonathan Pevsner, Forrest Spencer, Rafael A. Irizarry

Bioinform., 2011

2007

Pre-processing Agilent microarray data.

Marianna Zahurak, Giovanni Parmigiani, Wayne Yu, Robert B. Scharpf, David Berman, Edward Schaeffer, Shabana Shabbeer, Leslie Cope

BMC Bioinform., 2007

<i>SNPchip</i>: R classes and methods for SNP array data.

Robert B. Scharpf, Jason C. Ting, Jonathan Pevsner, Ingo Ruczinski

Bioinform., 2007