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| Bioinformatics Interpretation of Exome Sequencing: Blood Cancer |
| Jiwoong Kim, Yun-Gyeong Lee, Namshin Kim |
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Genomics Inform. 2013;11(1):24-33. Published online March 31, 2013 DOI: https://doi.org/10.5808/GI.2013.11.1.24 |
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Bioinformatics Interpretation of Exome Sequencing: Blood Cancer Genomics & Informatics. 2013;11(1):24  ERRATUM: Acknowledgments Correction. Bioinformatics Interpretation of Exome Sequencing: Blood Cancer Genomics & Informatics. 2013;11(2):98 Whole Exome Sequencing of Simultaneous Primary Multifocal Lung Cancer (SMPLC): Case Report and Bioinformatics Analysis . 2020; SeqGene: a comprehensive software solution for mining exome- and transcriptome- sequencing data BMC Bioinformatics. 2011;12(1): Exome Sequencing Dictionary of Bioinformatics and Computational Biology. 2004; An evaluation of copy number variation detection tools for cancer using whole exome sequencing data BMC Bioinformatics. 2017;18(1): Whole exome sequencing of pediatric gastric adenocarcinoma reveals an atypical presentation of Li-Fraumeni syndrome Pediatric Blood & Cancer. 2012;60(4):570-574 CoNVEX: copy number variation estimation in exome sequencing data using HMM BMC Bioinformatics. 2013;14(S2): Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors Pediatric Blood & Cancer. 2015;63(3):511-515 Exome Sequencing Data Analysis Encyclopedia of Bioinformatics and Computational Biology. 2019;164-175 |
