Thomas E. Royce, Ph.D.

Affiliations: 
Yale University, New Haven, CT 
Area:
Computational Biology and Bioinformatics
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"Thomas Royce"

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Mark B. Gerstein grad student 2007 Yale
 (Tiling microarray informatics.)
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Publications

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Basu GD, Drenner K, Ozols A, et al. (2020) Whole exome and transcriptome sequencing of colorectal and pancreatic cancer. Journal of Clinical Oncology. 38: e15666-e15666
Norman PJ, Norberg SJ, Guethlein LA, et al. (2017) Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II. Genome Research
Basu GD, White T, LoBello J, et al. (2017) Abstract 2779: Assessing germline and somatic alterations in DNA repair pathway in cancer Cancer Research. 77: 2779-2779
Roller E, Ivakhno S, Lee S, et al. (2016) Canvas: versatile and scalable detection of copy number variants. Bioinformatics (Oxford, England)
Basu GD, White T, LoBello JR, et al. (2016) ARID1A alterations in gastrointestinal cancers as therapeutic opportunities. Journal of Clinical Oncology. 34: 671-671
Norman PJ, Norberg SJ, Nemat-Gorgani N, et al. (2015) Very long haplotype tracts characterized at high resolution from HLA homozygous cell lines. Immunogenetics. 67: 479-85
Amini S, Pushkarev D, Christiansen L, et al. (2014) Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing. Nature Genetics. 46: 1343-9
Norman PJ, Norberg S, Royce T, et al. (2013) 148-P Human Immunology. 74: 151
Norman PJ, Norberg S, Nemat-Gorgani N, et al. (2013) 34-OR Human Immunology. 74: 26
Ivakhno S, Royce T, Cox AJ, et al. (2010) CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing data. Bioinformatics (Oxford, England). 26: 3051-8
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