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Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing

机译：通过多路复用CRAP-CAS9富集和长读数纳米孔测序检测合作伙伴独立的融合基因检测

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Christina Stangl; Sam de Blank; Ivo Renkens; Liset Westera; Tamara Verbeek; Jose Espejo Valle-Inclan; Rocio Chamorro González; Anton G. Henssen; Markus J. van Roosmalen; Ronald W. Stam; Emile E. Voest; Wigard P. Kloosterman; Gijs van Haaften; Glen R. Monroe;
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1. Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing [J] . Christina Stangl, Sam de Blank, Ivo Renkens, Nature Communications . 2020,第1期

机译：通过多路复用CRAP-CAS9富集和长读数纳米孔测序检测合作伙伴独立的融合基因检测
2. Detection of a Complex EML4-ALK Fusion Transcript Via Anchored Multiplex PCR and de novo Assembly of Next-Generation Sequencing Reads [J] . Davies K. D., Mann P. R., Le A. T., The Journal of molecular diagnostics: JMD . 2016,第6期

机译：通过锚定多重PCR和新一代测序读物的从头组装检测复杂的EML4-ALK融合转录本
3. MinION (R) multiplex long read nanopore sequencing: an innovative and effective tool for thiopurine pharmacogenetics [J] . Fundamental & clinical pharmacology. . 2019,第S1期

机译：Minion（R）多重长读数纳米孔测序：硫嘌呤药物遗传学的创新有效工具
4. NanoBLASTer: Fast alignment and characterization of Oxford Nanopore single molecule sequencing reads [C] . Mohammad Ruhul Amin, Steven Skiena, Michael C. Schatz IEEE International Conference on Computational Advances in Bio and Medical Sciences . 2016

机译：NanoBLASTer：牛津纳米孔单分子测序读物的快速比对和表征
5. Nanopore DNA sequencing and epigenetic detection with a MspA nanopore [D] . Laszlo, Andrew H. 2014

机译：纳米孔DNA测序和MspA纳米孔的表观遗传检测
6. Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing [O] . Christina Stangl, Sam de Blank, Ivo Renkens, -1

机译：通过多重CRISPR-Cas9富集和长读纳米孔测序来检测伴侣独立的融合基因
7. Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for Rapid, Accurate, and Affordable Somatic Mutation Detection [O] . Deepak Thirunavukarasu, Lauren Y. Cheng, Ping Song, 2020

机译：癌基因串联富集扩增子纳米孔测序，用于快速，准确，实惠的体细胞突变检测

Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing

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