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Clinical Validation of a Myeloid Next-Generation Sequencing Panel for Single-Nucleotide Variants, Insertions/Deletions, and Fusion Genes

机译：单核苷酸变体，插入/缺失和融合基因的骨髓下一代测序面板的临床验证

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Iyare Izevbaye; Li Y. Liang; Cheryl Mather; Soufiane El-Hallani; Remegio Maglantay; Lalit Saini;
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1. Clinical Validation of a Myeloid Next-Generation Sequencing Panel for Single-Nucleotide Variants, Insertions/Deletions, and Fusion Genes [J] . Izevbaye Iyare, Liang Li Y., Mather Cheryl, The Journal of molecular diagnostics: JMD . 2020,第2期

机译：单核苷酸变体，插入/缺失和融合基因的骨髓下一代测序面板的临床验证
2. Clinical Validation of a Comprehensive DNA/RNA Panel (170 Genes) for Single Nucleotide Variants (SNVs), Small Insertions/Deletions (Indels), Copy Number Variations (CNVs) Splice Variations (SVs), and Gene Fusions (GF) on an NGS Platform in a CLIA Setting. [J] . Kolhe R., Mondal A. K., Pundkar C., The Journal of molecular diagnostics: JMD . 2018,第6期

机译：单个核苷酸变体（SNV），小插入/缺失（诱导），拷贝数变异（CNV）剪切变异（SVS）和基因融合（GF）对NGS的临床验证平台在Clia设置。
3. Technical Validation of a Next-Generation Sequencing Assay for Detecting Clinically Relevant Levels of Breast Cancer-Related Single-Nucleotide Variants and Copy Number Variants Using Simulated Cell-Free DNA [J] . Yang Xin, Chu Yuxing, Zhang Rui, The Journal of molecular diagnostics: JMD . 2017,第4期

机译：用于检测临床相关水平的乳腺癌相关单核苷酸变体和拷贝数变体的下一代测序测定的技术验证使用模拟无细胞DNA
4. An Effective and Efficient Algorithm for Detecting Exact Deletion Breakpoints from Viral Next-Generation Sequencing Data [C] . Ji-Hong Cheng, Wen-Chun Liu, Ting-Tsung Chang, International Computer Symposium . 2020

机译：一种有效且有效的算法，用于检测病毒下一代测序数据的精确删除断点
5. Probabilistic insertion, deletion and substitution error correction using Markov inference in next generation sequencing reads [D] . Noroozi, Vahid 2016

机译：在下一代测序读取中使用马尔可夫推论进行概率插入，删除和取代错误校正
6. Guideline-Adherent Clinical Validation of a Comprehensive 170-Gene DNA/RNA Panel for Determination of Small Variants Copy Number Variations Splice Variants and Fusions on a Next-Generation Sequencing Platform in the CLIA Setting [O] . Theresa A. Boyle, Ashis K. Mondal, Daryoush Saeed-Vafa, 2021

机译：综合170-基因DNA / RNA面板的指导鉴定临床验证用于测定CLIA设置下一代测序平台上的小变体拷贝数变异剪接变体和融合
7. Simultaneous detection of single-nucleotide variant, deletion/insertion, and fusion in lung and thyroid carcinoma using cytology specimen and an RNA-based next-generation sequencing assay [O] . Natalya V. Guseva, Omar Jaber, Aaron A. Stence, 2018

机译：使用细胞学标本和基于RNA的下一代测序测定，同时检测肺和甲状腺癌中的单核苷酸变体，缺失/插入和融合

Clinical Validation of a Myeloid Next-Generation Sequencing Panel for Single-Nucleotide Variants, Insertions/Deletions, and Fusion Genes

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