首页> 外文OA文献 >Figure 2: Mutational exposures and three mutational signatures from the analysis of 16 trunk mutational catalogs and 16 branch mutational catalogs in the USC data (16 colon cancer patients).

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Figure 2: Mutational exposures and three mutational signatures from the analysis of 16 trunk mutational catalogs and 16 branch mutational catalogs in the USC data (16 colon cancer patients).

机译：图2：来自USC数据中16个中继突发目录和16分支突变目录的分析（16例结肠癌患者）的分析中的突变暴露和三种突变签名。

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1. Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations [J] . Elisa A Colombo, J Fernando Bazan, Gloria Negri, Orphanet journal of rare diseases . 2012,第S1期

机译：中性粒细胞减少症的鬼臼病患者的新C16orf57突变：蛋白质的生物信息学分析和所有报道的突变的预测作用
2. The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease [J] . Elson Joanna L., Smith Paul M., Greaves Laura C., Mitochondrion . 2015,第Null期

机译：临床样品中高度破坏性的16S rRNA突变的存在表明线粒体核糖体突变在人类疾病中的作用更加广泛
3. Mutational analysis of PAX6: 16 novel mutations including 5 missense mutations with a mild aniridia phenotype. [J] . Gronskov K, Rosenberg T, Sand A, European journal of human genetics: EJHG . 1999,第3期

机译：PAX6的突变分析：16个新突变，包括5个具有轻度无虹膜表型的错义突变。
4. Identification of potential long non-coding RNA biomarkers for breast cancer patients with somatic BRCA1 mutations from RNA-Seq datasets [C] . Jia-Hua Cai, Yu-Ching Chen, Hsueh-Ting Chu, IEEE International Conference on Bioinformatics and Bioengineering . 2018

机译：鉴定来自RNA-SEQ数据集的乳腺癌患者乳腺癌患者的潜在长期非编码RNA生物标志物
5. Mutational analysis of the E5 protein of human papillomavirus type 16 to analyze the role of interaction with the 16-kDa subunit of the vacuolar H(+)-ATPase in inhibiting activity of this complex and altering metabolism of the epidermal growth factor receptor. [D] . Adam, Jamie L. 2000

机译：人类乳头瘤病毒16型E5蛋白的突变分析，以分析与液泡H（+）-ATPase的16-kDa亚基相互作用在抑制该复合物活性和改变表皮生长因子受体代谢中的作用。
6. GENE-16. CLINICALLY AGGRESSIVE MENINGIOMAS ARE CHARACTERIZED BY MUTATIONAL SIGNATURES ASSOCIATED WITH DEFECTIVE DNA REPAIR AND MUTATIONS IN CHROMATIN REMODELING GENES [O] . Sylvia Kurz, Benjamin Liechty, Stephen Kelly, -1

机译：基因16。临床上广泛的脑膜瘤是通过与缺陷DNA修复和染色质重塑基因突变相关的突变信号来表征的。
7. Figure S2: The result of estimating mutational signatures for the USC data, including 16 trunk mutational catalogs and 16 branch mutational catalogs, using different values of K, the number of mutational signatures [O] . -1

机译：图S2：估计USC数据的突变签名的结果，包括16个中继突变目录和16分支突变目录，使用不同的k值，突变签名的数量

Figure 2: Mutational exposures and three mutational signatures from the analysis of 16 trunk mutational catalogs and 16 branch mutational catalogs in the USC data (16 colon cancer patients).

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