Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays

por Oldridge, Derek A., Banerjee, Samprit, Setlur, Sunita R., Sboner, Andrea, Demichelis, Francesca
Publicado 2010

Defining fallopian tube‐derived miRNA cancer signatures

por Dejene, Selam B., Ohman, Anders W., Du, Wei, Randhawa, Deepinder, Bradley, Anand, Yadav, Niraj, Elias, Kevin M., Dinulescu, Daniela M., Setlur, Sunita R.
Publicado 2019

Association of CNVs with methylation variation

por Shi, Xinghua, Radhakrishnan, Saranya, Wen, Jia, Chen, Jin Yun, Chen, Junjie, Lam, Brianna Ashlyn, Mills, Ryan E., Stranger, Barbara E., Lee, Charles, Setlur, Sunita R.
Publicado 2020

Molecular sampling of prostate cancer: a dilemma for predicting disease progression

por Sboner, Andrea, Demichelis, Francesca, Calza, Stefano, Pawitan, Yudi, Setlur, Sunita R, Hoshida, Yujin, Perner, Sven, Adami, Hans-Olov, Fall, Katja, Mucci, Lorelei A, Kantoff, Philip W, Stampfer, Meir, Andersson, Swen-Olof, Varenhorst, Eberhard, Johansson, Jan-Erik, Gerstein, Mark B, Golub, Todd R, Rubin, Mark A, Andrén, Ove
Publicado 2010