Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes
| Autor: | Kumar S, Udhaya, Balasundaram, Ambritha, Cathryn R, Hephzibah, Varghese, Rinku Polachirakkal, R, Siva, R, Gnanasambandan, Younes, Salma, Zayed, Hatem, Doss C, George Priya |
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| Zdroj: | In Computers in Biology and Medicine September 2022 148 |
| Databáze: | ScienceDirect |
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