Cite
Locus co-occupancy, nucleosome positioning, and H3K4me1 regulate the functionality of FOXA2-, HNF4A-, and PDX1-bound loci in islets and liver.
MLA
Hoffman, Brad G., et al. “Locus Co-Occupancy, Nucleosome Positioning, and H3K4me1 Regulate the Functionality of FOXA2-, HNF4A-, and PDX1-Bound Loci in Islets and Liver.” Genome Research, vol. 20, no. 8, Aug. 2010, p. 4. EBSCOhost, https://doi.org/10.1101/gr.104356.109.
APA
Hoffman, B. G., Robertson, G., Zavaglia, B., Beach, M., Cullum, R., Lee, S., Soukhatcheva, G., Leping Li, Wederell, E. D., Thiessen, N., Bilenky, M., Cezard, T., Tam, A., Kamoh, B., Birol, I., Dai, D., YongJun Zhao, Hirst, M., Helgason, C. D., & Marra, M. A. (2010). Locus co-occupancy, nucleosome positioning, and H3K4me1 regulate the functionality of FOXA2-, HNF4A-, and PDX1-bound loci in islets and liver. Genome Research, 20(8), 4. https://doi.org/10.1101/gr.104356.109
Chicago
Hoffman, Brad G., Gordon Robertson, Bogard Zavaglia, Mike Beach, Rebecca Cullum, Sam Lee, Galina Soukhatcheva, et al. 2010. “Locus Co-Occupancy, Nucleosome Positioning, and H3K4me1 Regulate the Functionality of FOXA2-, HNF4A-, and PDX1-Bound Loci in Islets and Liver.” Genome Research 20 (8): 4. doi:10.1101/gr.104356.109.