Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes. - S. Udhaya Kumar; Ambritha Balasundaram; Cathryn R. Hephzibah; Rinku Polachirakkal Varghese; R. Siva; Gnanasambandan Ramanathan; Salma Younes; Hatem Zayed; C. George Priya Doss (Comput. Biol. Medicine, 2022)