Thomas E. Royce, Ph.D.
Affiliations: | Yale University, New Haven, CT |
Area:
Computational Biology and BioinformaticsGoogle:
"Thomas Royce"Parents
Sign in to add mentor| 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 |