Ng, Pauline C

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Kumar, P., Henikoff, S., & Ng, P. C. (2009) · Nature Protocols

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

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The Diploid Genome Sequence of an Individual Human

Levy, S., Sutton, G., Ng, P. C., Feuk, L., Halpern, A. L., Walenz, B. P., Axelrod, N., Huang, J., Kirkness, E. F., Denisov, G., et al. (2007) · PLoS Biology

Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities

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SIFT missense predictions for genomes

Vaser, R., Adusumalli, S., Leng, S. N., Sikic, M., & Ng, P. C. (2016) · Nature Protocols

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

Cited by 1,510

Evaluation of next generation sequencing platforms for population targeted sequencing studies

Harismendy, O., Ng, P. C., Strausberg, R. L., Wang, X., Stockwell, T. B., Beeson, K. Y., Schork, N. J., Murray, S. S., Topol, E. J., Levy, S., et al. (2009) · Genome Biology

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

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An agenda for personalized medicine

Ng, P. C., Murray, S. S., Levy, S., & Venter, J. C. (2009) · Nature

Biomedical Ethics and RegulationGenomics and Rare Diseases

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