Predrag Radivojac, Ph.D.
Affiliations: | 2004 | Temple University, Philadelphia, PA, United States |
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"Predrag Radivojac"Parents
Sign in to add mentor| Zoran Obradovic | grad student | 2004 | Temple University | |
| (Classification and knowledge discovery in protein databases.) | ||||
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Publications
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| Ramola R, Friedberg I, Radivojac P. (2022) The field of protein function prediction as viewed by different domain scientists. Bioinformatics Advances. 2: vbac057 |
| Radivojac P. (2022) Advancing remote homology detection: A step toward understanding and accurately predicting protein function. Cell Systems. 13: 435-437 |
| Pejaver V, Urresti J, Lugo-Martinez J, et al. (2020) Inferring the molecular and phenotypic impact of amino acid variants with MutPred2. Nature Communications. 11: 5918 |
| Stamboulian M, Guerrero RF, Hahn MW, et al. (2020) The ortholog conjecture revisited: the value of orthologs and paralogs in function prediction. Bioinformatics (Oxford, England). 36: i219-i226 |
| Zhou N, Jiang Y, Bergquist TR, et al. (2019) The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens. Genome Biology. 20: 244 |
| Clark WT, Kasak L, Bakolitsa C, et al. (2019) Assessment of predicted enzymatic activity of alpha-N-acetylglucosaminidase (NAGLU) variants of unknown significance for CAGI 2016. Human Mutation |
| Kasak L, Hunter JM, Udani R, et al. (2019) CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases. Human Mutation |
| Kasak L, Bakolitsa C, Hu Z, et al. (2019) Assessing Computational Predictions of the Phenotypic Effect of Cystathionine-beta-Synthase Variants. Human Mutation |
| Cline MS, Babbi G, Bonache S, et al. (2019) Assessment of blind predictions of the clinical significance of BRCA1 and BRCA2 variants. Human Mutation |
| Voskanian A, Katsonis P, Lichtarge O, et al. (2019) Assessing the performance of in-silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer. Human Mutation |