Dr. Shuli Kang
Novartis Gene Therapies, USA
Email:
[email protected] (preferred), [email protected]
Qualifications
2008 Ph.D., Microbiology, Wuhan University, China
2003 B.Sc., National Education Base of Life Sciences,
Wuhan University, China
Publications (Selected)
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Li, W., Li, Q., Kang, S., Same, M., Zhou, Y., Sun, C., ... & Zhou, X. J. (2018). CancerDetector: ultrasensitive and non-invasive cancer detection at the resolution of individual reads using cell-free DNA methylation sequencing data. Nucleic acids research, 46(15), e89-e89.
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Kang, S., Li, Q., Chen, Q., Zhou, Y., Park, S., Lee, G., ... & Zhou, X. J. (2017). CancerLocator: non-invasive cancer diagnosis and tissue-of-origin prediction using methylation profiles of cell-free DNA. Genome biology, 18, 1-12.
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Yang, X., Coulombe-Huntington, J., Kang, S., Sheynkman, G. M., Hao, T., Richardson, A., ... & Vidal, M. (2016). Widespread expansion of protein interaction capabilities by alternative splicing. Cell, 164(4), 805-817.
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Li, W., Liu, C. C., Kang, S., Li, J. R., Tseng, Y. T., & Zhou, X. J. (2016). Pushing the annotation of cellular activities to a higher resolution: Predicting functions at the isoform level. Methods, 93, 110-118.
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Rolland, T., Taşan, M., Charloteaux, B., Pevzner, S. J., Zhong, Q., Sahni, N., ... & Vidal, M. (2014). A proteome-scale map of the human interactome network. Cell, 159(5), 1212-1226.
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Li, W., Dai, C., Kang, S., & Zhou, X. J. (2014). Integrative analysis of many RNA-seq datasets to study alternative splicing. Methods, 67(3), 313-324.
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Corominas, R., Yang, X., Lin, G. N., Kang, S., Shen, Y., Ghamsari, L., ... & Iakoucheva, L. M. (2014). Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism. Nature communications, 5(1), 3650.
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Li, W., Kang, S., Liu, C. C., Zhang, S., Shi, Y., Liu, Y., & Zhou, X. J. (2014). High-resolution functional annotation of human transcriptome: predicting isoform functions by a novel multiple instance-based label propagation method. Nucleic acids research, 42(6), e39-e39.
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Michaelson, J. J., Shi, Y., Gujral, M., Zheng, H., Malhotra, D., Jin, X., ... & Sebat, J. (2012). Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. Cell, 151(7), 1431-1442.
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Liao, Q., Liu, C., Yuan, X., Kang, S., Miao, R., Xiao, H., ... & Zhao, Y. (2011). Large-scale prediction of long non-coding RNA functions in a coding–non-coding gene co-expression network. Nucleic acids research, 39(9), 3864-3878.
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Mills, R. E., Walter, K., Stewart, C., Handsaker, R. E., Chen, K., Alkan, C., ... & 1000 Genomes Project. (2011). Mapping copy number variation by population-scale genome sequencing. Nature, 470(7332), 59-65.
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Yuan, X., Liu, C., Yang, P., He, S., Liao, Q., Kang, S., & Zhao, Y. (2009). Clustered microRNAs' coordination in regulating protein-protein interaction network. BMC systems biology, 3, 1-10.
Profile Details
https://www.linkedin.com/in/shulik/
https://scholar.google.com/citations?user=cty0KFUAAAAJ&hl=en
https://www.researchgate.net/profile/Shuli-Kang