Ingo Ruczinski

According to our database, Ingo Ruczinski authored at least 8 papers between 2006 and 2022.

Collaborative distances:

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

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

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

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

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

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

Bioinform., 2007

2006

Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.

Jason C. Ting, Ying Ye, George H. Thomas, Ingo Ruczinski, Jonathan Pevsner

BMC Bioinform., 2006