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Journal Articles
- 2022
[j8]Athena Chen
, Kai Kammers, H. Benjamin Larman, Robert B. Scharpf, Ingo Ruczinski:
Detecting and quantifying antibody reactivity in PhIP-Seq data with BEER. Bioinform. 38(19): 4647-4649 (2022)- 2019
- [j7]Jack M. Fu, Elizabeth J. Leslie, Alan F. Scott, Jeffrey C. Murray, Mary L. Marazita, Terri H. Beaty, Robert B. Scharpf, Ingo Ruczinski:
Detection of de novo copy number deletions from targeted sequencing of trios. Bioinform. 35(4): 571-578 (2019) - [j6]Thomas Sherman, Jack M. Fu, Robert B. Scharpf, Alexandre Bureau, Ingo Ruczinski:
Detection of rare disease variants in extended pedigrees using RVS. Bioinform. 35(14): 2509-2511 (2019) - 2014
- [j5]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:
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinform. 30(15): 2189-2196 (2014) - 2012
- [j4]Robert B. Scharpf, Terri H. Beaty, Holger Schwender, Samuel G. Younkin, Alan F. Scott, Ingo Ruczinski:
Fast detection of de novo copy number variants from SNP arrays for case-parent trios. BMC Bioinform. 13: 330 (2012) - 2011
- [j3]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:
Performance assessment of copy number microarray platforms using a spike-in experiment. Bioinform. 27(8): 1052-1060 (2011) - 2007
- [j2]Robert B. Scharpf, Jason C. Ting, Jonathan Pevsner, Ingo Ruczinski:
SNPchip: R classes and methods for SNP array data. Bioinform. 23(5): 627-628 (2007) - 2006
- [j1]Jason C. Ting, Ying Ye, George H. Thomas, Ingo Ruczinski, Jonathan Pevsner:
Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan. BMC Bioinform. 7: 25 (2006)
Coauthor Index
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