Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

di McKernan, Kevin Judd, Peckham, Heather E., Costa, Gina L., McLaughlin, Stephen F., Fu, Yutao, Tsung, Eric F., Clouser, Christopher R., Duncan, Cisyla, Ichikawa, Jeffrey K., Lee, Clarence C., Zhang, Zheng, Ranade, Swati S., Dimalanta, Eileen T., Hyland, Fiona C., Sokolsky, Tanya D., Zhang, Lei, Sheridan, Andrew, Fu, Haoning, Hendrickson, Cynthia L., Li, Bin, Kotler, Lev, Stuart, Jeremy R., Malek, Joel A., Manning, Jonathan M., Antipova, Alena A., Perez, Damon S., Moore, Michael P., Hayashibara, Kathleen C., Lyons, Michael R., Beaudoin, Robert E., Coleman, Brittany E., Laptewicz, Michael W., Sannicandro, Adam E., Rhodes, Michael D., Gottimukkala, Rajesh K., Yang, Shan, Bafna, Vineet, Bashir, Ali, MacBride, Andrew, Alkan, Can, Kidd, Jeffrey M., Eichler, Evan E., Reese, Martin G., De La Vega, Francisco M., Blanchard, Alan P.
Pubblicazione 2009