Education

Ph.D., Stanford School of Medicine, USA, 2017

Current position

Post-doc, Pathology, Stanford School of Medicine, USA

Publications

1. Fu, B. X., Wainberg, M., Kundaje, A. and Fire, A. Z. (2017). High-Throughput Characterization of Cascade type I-E CRISPR Guide Efficacy Reveals Unexpected PAM Diversity and Target Sequence Preferences. Genetics 206(4): 1727-1738.
2. Fu, B. X., St Onge, R. P., Fire, A. Z. and Smith, J. D. (2016). Distinct patterns of Cas9 mismatch tolerance in vitro and in vivo. Nucleic Acids Res 44(11): 5365-5377.
3. Bell, R. T., Fu, B. X. and Fire, A. Z. (2016). Cas9 Variants Expand the Target Repertoire in Caenorhabditis elegans. Genetics 202(2): 381-388.
4. Meyer, D., Fu, B. X. and Heyer, W. D. (2015). DNA polymerases delta and lambda cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A 112(50): E6907-6916.
5. Fu, B. X., Hansen, L. L., Artiles, K. L., Nonet, M. L. and Fire, A. Z. (2014). Landscape of target:guide homology effects on Cas9-mediated cleavage. Nucleic Acids Res 42(22): 13778-13787.
6. Arribere, J. A., Bell, R. T., Fu, B. X., Artiles, K. L., Hartman, P. S. and Fire, A. Z. (2014). Efficient marker-free recovery of custom genetic modifications with CRISPR/Cas9 in Caenorhabditis elegans. Genetics 198(3): 837-846.
7. Liddell, L. C., Manthey, G. M., Owens, S. N., Fu, B. X. and Bailis, A. M. (2013). Alleles of the homologous recombination gene, RAD59, identify multiple responses to disrupted DNA replication in Saccharomyces cerevisiae. BMC Microbiol 13: 229.
8. Pannunzio, N. R., Manthey, G. M., Liddell, L. C., Fu, B. X., Roberts, C. M. and Bailis, A. M. (2012). Rad59 regulates association of Rad52 with DNA double-strand breaks. Microbiologyopen 1(3): 285-297.