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Detecting Rare AID-Induced Mutations in B-Lineage Oncogenes from High-Throughput Sequencing Data Using the Detection of Minor Variants by Error Correction Method

机译：通过误差校正方法检测来自高通量测序数据的B型血管生成的罕见辅助诱导突变

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Ophélie Alyssa Martin; Armand Garot; Sandrine Le Noir; Jean-Claude Aldigier; Michel Cogné; Eric Pinaud; François Boyer;
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年度 2018
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1. Detecting Rare AID-Induced Mutations in B-Lineage Oncogenes from High-Throughput Sequencing Data Using the Detection of Minor Variants by Error Correction Method [J] . Martin Ophelie Alyssa, Garot Armand, Le Noir Sandrine, The Journal of Immunology: Official Journal of the American Association of Immunologists . 2018,第3期

机译：通过误差校正方法检测来自高通量测序数据的B型血管生成的罕见辅助诱导突变
2. Machine learning models in error and variant detection in high-variation high-throughput sequencing datasets [J] . Milko Krachunov, Maria Nisheva, Dimitar Vassilev Procedia Computer Science . 2017,第期

机译：高变高吞吐量排序数据集的误差和变体检测机器学习模型
3. GxGrare: gene-gene interaction analysis method for rare variants from high-throughput sequencing data [J] . Minseok Kwon, Sangseob Leem, Joon Yoon, BMC Systems Biology . 2018,第2期

机译：GxGrare：高通量测序数据中罕见变异的基因-基因相互作用分析方法
4. A* fast and scalable high-throughput sequencing data error correction via oligomers [C] . Franco Milicchio, Iain E. Buchan, Mattia C.F. Prosperi IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology . 2016

机译：通过低聚物实现快速，可扩展的高通量测序数据纠错
5. Computational assessment of somatic missense mutations detected in tumor sequencing studies with cancer-specific high-throughput annotation of somatic mutations (CHASM). [D] . Carter, Hannah. 2012

机译：具有肿瘤特异性高通量体细胞突变（CHASM）的肿瘤测序研究中检测到的体细胞错义突变的计算评估。
6. Inflated Type I Error Rates When Using Aggregation Methods to Analyze Rare Variants in the 1000 Genomes Project Exon Sequencing Data in Unrelated Individuals: Summary Results from Group 7 at Genetic Analysis Workshop 17 [O] . Nathan Tintle, Hugues Aschard, Inchi Hu, -1

机译：使用聚集方法时膨胀I型错误率分析1000个基因组项目外显子测序数据中的稀有变体：在遗传分析研讨会上的第7组摘要结果17
7. Denoising DNA deep sequencing data—high-throughput sequencing errors and their correction [O] . David Laehnemann, Arndt Borkhardt, Alice Carolyn McHardy 2015

机译：去噪DNA深度测序数据 - 高通量测序误差及其校正
8. New Sieving Matrix for DNA Sequencing, Genotyping and Mutation Detection and High-Throughput Genotyping with a 96-Capillary Array System [R] . Gao, D. 1999

机译：使用96-毛细管阵列系统进行DNa测序，基因分型和突变检测以及高通量基因分型的新筛选矩阵

Detecting Rare AID-Induced Mutations in B-Lineage Oncogenes from High-Throughput Sequencing Data Using the Detection of Minor Variants by Error Correction Method

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