A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing

por Mijušković, Martina, Brown, Stuart M., Tang, Zuojian, Lindsay, Cory R., Efstathiadis, Efstratios, Deriano, Ludovic, Roth, David B.
Publicado 2012

Information content and analysis methods for Multi-Modal High-Throughput Biomedical Data

por Ray, Bisakha, Henaff, Mikael, Ma, Sisi, Efstathiadis, Efstratios, Peskin, Eric R., Picone, Marco, Poli, Tito, Aliferis, Constantin F., Statnikov, Alexander
Publicado 2014