Biao Li

发表

In silico functional profiling of human disease‐associated and polymorphic amino acid substitutions

Peter H. Baenziger, Kishore K. Kamati, Uday S. Evani, 2010, Human mutation.

Bioinformatics Approaches to the Functional Proﬁling of Genetic Variants

P. Radivojac, S. Mooney, Biao Li, 2012 .

MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing

P. Radivojac, S. Mooney, D. Cooper, 2014, Genome Biology.

Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways

Sean D. Mooney, Birgit Schilling, Matthew J. Rardin, 2013, Proceedings of the National Academy of Sciences.

In silico comparative characterization of pharmacogenomic missense variants

M. Whirl‐Carrillo, E. Capriotti, S. Mooney, 2014, BMC Genomics.

Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential

P. Radivojac, Biao Li, D. Samuels, 2014, Scientific Reports.

Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges

Silvio C. E. Tosatto, Hui Ting Grace Yeo, Madeleine P. Ball, 2017, Human mutation.

Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

Alexander A. Morgan, Yanay Ofran, Predrag Radivojac, 2017, Human mutation.

Calibration of Multiple In Silico Tools for Predicting Pathogenicity of Mismatch Repair Gene Missense Substitutions

Predrag Radivojac, Biao Li, Alun Thomas, 2013, Human mutation.

MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing

P. Radivojac, S. Mooney, D. Cooper, 2014, Genome Biology.

In silico prediction of deleterious single amino acid polymorphisms from amino acid sequence

Biao Li, Shuyan Li, Huanxiang Liu, 2011, J. Comput. Chem..

Evaluating Purifying Selection in the Mitochondrial DNA of Various Mammalian Species

P. Radivojac, Biao Li, V. Macaulay, 2013, PloS one.

Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity.

Predrag Radivojac, Biao Li, Luísa Pereira, 2011, American journal of human genetics.

Automated inference of molecular mechanisms of disease from amino acid substitutions

Predrag Radivojac, Biao Li, Sean D. Mooney, 2009, Bioinform..

A Large Scale Huntingtin Protein Interaction Network Implicates Rho GTPase Signaling Pathways in Huntington Disease*♦

Sean D. Mooney, Biao Li, Russell Bell, 2014, The Journal of Biological Chemistry.

Optimizing the Molecular Diagnosis of GALNS: Novel Methods to Define and Characterize Morquio—A Syndrome‐Associated Mutations

S. Mooney, S. Bianca, Biao Li, 2015, Human mutation.

A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing

Cheng Wang, Biao Li, Sean D. Mooney, 2014, PLoS Comput. Biol..

An expanded evaluation of protein function prediction methods shows an improvement in accuracy

Tapio Salakoski, Paolo Fontana, Silvio C. E. Tosatto, 2016, Genome Biology.

Tau/MAPT disease-associated variant A152T alters tau function and toxicity via impaired retrograde axonal transport

A. Burlingame, S. Mooney, Victoria J. Butler, 2018, Human molecular genetics.

Disease GTPase Signaling Pathways in Huntington Interaction Network Implicates Rho A Large Scale Huntingtin Protein Molecular Bases of Disease

S. Mooney, L. Kaltenbach, R. Bell, 2014 .

Optimizing the Molecular Diagnosis of GALNS: Novel Methods to Define and Characterize Morquio—A Syndrome‐Associated Mutations

S. Mooney, S. Bianca, Biao Li, 2015, Human mutation.

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

Silvio C. E. Tosatto, Julius O. B. Jacobsen, Nicholas A. Sinnott-Armstrong, 2024, Genome biology.

The Aquila Digital Community The Aquila Digital Community

Silvio C. E. Tosatto, Karin M. Verspoor, David A. Lee, 2022 .

Calibration of Multiple In Silico Tools for Predicting Pathogenicity of Mismatch Repair Gene Missense Substitutions

P. Radivojac, S. Mooney, S. Sunyaev, 2013, Human mutation.