Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes.
S. Udhaya KumarAmbritha BalasundaramCathryn R. HephzibahRinku Polachirakkal VargheseR. SivaR. GnanasambandanSalma YounesHatem ZayedC. George Priya DossPublished in: Comput. Biol. Medicine (2022)