The Current State and Future of CRISPR-Cas9 gRNA Design Tools
暂无分享,去创建一个
[1] J. Keith Joung,et al. Improving CRISPR-Cas nuclease specificity using truncated guide RNAs , 2014, Nature Biotechnology.
[2] Henriette O'Geen,et al. A genome-wide analysis of Cas9 binding specificity using ChIP-seq and targeted sequence capture , 2014, bioRxiv.
[3] Matthew C. Canver,et al. Impact of Genetic Variation on CRISPR-Cas Targeting. , 2018, The CRISPR journal.
[4] Lei S. Qi,et al. The New State of the Art: Cas9 for Gene Activation and Repression , 2015, Molecular and Cellular Biology.
[5] Matthew C. Canver,et al. Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci , 2017, Nature Genetics.
[6] L. Zhu,et al. CRISPRseek: A Bioconductor Package to Identify Target-Specific Guide RNAs for CRISPR-Cas9 Genome-Editing Systems , 2014, PloS one.
[7] Max A. Horlbeck,et al. Nucleosomes impede Cas9 access to DNA in vivo and in vitro , 2016, eLife.
[8] E. Lander,et al. Genetic Screens in Human Cells Using the CRISPR-Cas9 System , 2013, Science.
[9] B. Davies,et al. CRISPR-Cas orthologues and variants: optimizing the repertoire, specificity and delivery of genome engineering tools , 2017, Mammalian Genome.
[10] J. Joung,et al. CIRCLE-seq: a highly sensitive in vitro screen for genome-wide CRISPR-Cas9 nuclease off-targets , 2017, Nature Methods.
[11] Toshio Ando,et al. Real-space and real-time dynamics of CRISPR-Cas9 visualized by high-speed atomic force microscopy , 2017, Nature Communications.
[12] Denis C. Bauer,et al. High Activity Target-Site Identification Using Phenotypic Independent CRISPR-Cas9 Core Functionality. , 2018, The CRISPR journal.
[13] Charles E. Vejnar,et al. CRISPRscan: designing highly efficient sgRNAs for CRISPR/Cas9 targeting in vivo , 2015, Nature Methods.
[14] James A. Gagnon,et al. Efficient CRISPR-Cas9-mediated generation of knockin human pluripotent stem cells lacking undesired mutations at the targeted locus. , 2015, Cell reports.
[15] J. Keith Joung,et al. High frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells , 2013, Nature Biotechnology.
[16] J. Doudna,et al. A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity , 2012, Science.
[17] Max A. Horlbeck,et al. Compact and highly active next-generation libraries for CRISPR-mediated gene repression and activation , 2016, eLife.
[18] Eli J. Fine,et al. DNA targeting specificity of RNA-guided Cas9 nucleases , 2013, Nature Biotechnology.
[19] Shailesh Sharma,et al. SSFinder: high throughput CRISPR-Cas target sites prediction tool. , 2014 .
[20] David M. Reif,et al. Machine Learning for Detecting Gene-Gene Interactions , 2006, Applied bioinformatics.
[21] Nicole M. Gaudelli,et al. Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage , 2017, Nature.
[22] David A. Scott,et al. Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells , 2014, Nature Biotechnology.
[23] J. Kent,et al. Evaluation of off-target and on-target scoring algorithms and integration into the guide RNA selection tool CRISPOR , 2016, Genome Biology.
[24] James E. DiCarlo,et al. RNA-Guided Human Genome Engineering via Cas9 , 2013, Science.
[25] W. Lim,et al. Nucleosome breathing and remodeling constrain CRISPR-Cas9 function , 2016, eLife.
[26] Leslie S. Edwards,et al. Mapping the genomic landscape of CRISPR–Cas9 cleavage , 2017, Nature Methods.
[27] Martin J. Aryee,et al. GUIDE-Seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases , 2014, Nature Biotechnology.
[28] Sangsu Bae,et al. Microhomology-based choice of Cas9 nuclease target sites , 2014, Nature Methods.
[29] David A. Scott,et al. Implications of human genetic variation in CRISPR-based therapeutic genome editing , 2017, Nature Medicine.
[30] Jin-Soo Kim,et al. Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases , 2014, Bioinform..
[31] Jennifer Listgarten,et al. Prediction of off-target activities for the end-to-end design of CRISPR guide RNAs , 2018, Nature Biomedical Engineering.
[32] Daniel Capurso,et al. DNA Repair Profiling Reve als Nonrandom Outcomes at Cas 9-Mediated Breaks Graphical Abstract Highlights , 2016 .
[33] Meagan E. Sullender,et al. Rational design of highly active sgRNAs for CRISPR-Cas9–mediated gene inactivation , 2014, Nature Biotechnology.
[34] Mazhar Adli,et al. Genome-wide analysis reveals characteristics of off-target sites bound by the Cas9 endonuclease , 2014, Nature Biotechnology.
[35] Yilong Li,et al. Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library , 2013, Nature Biotechnology.
[36] Qiang Sun,et al. Homology-mediated end joining-based targeted integration using CRISPR/Cas9 , 2017, Cell Research.
[37] Rongchen Wang,et al. Production of Guide RNAs in vitro and in vivo for CRISPR Using Ribozymes and RNA Polymerase II Promoters. , 2017, Bio-protocol.
[38] H. Kim,et al. A guide to genome engineering with programmable nucleases , 2014, Nature Reviews Genetics.
[39] Le Cong,et al. Multiplex Genome Engineering Using CRISPR/Cas Systems , 2013, Science.
[40] Meagan E. Sullender,et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9 , 2015, Nature Biotechnology.
[41] Xiaowei Wang,et al. WU-CRISPR: characteristics of functional guide RNAs for the CRISPR/Cas9 system , 2015, Genome Biology.
[42] Itay Mayrose,et al. A machine learning approach for predicting CRISPR-Cas9 cleavage efficiencies and patterns underlying its mechanism of action , 2017, PLoS Comput. Biol..
[43] Steven Salzberg,et al. Short Read Mapping: An Algorithmic Tour , 2017, Proceedings of the IEEE.
[44] G. Church,et al. Unraveling CRISPR-Cas9 genome engineering parameters via a library-on-library approach , 2015, Nature Methods.
[45] Jean-Claude Tardif,et al. Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci , 2017, Proceedings of the National Academy of Sciences.
[46] Mazhar Adli,et al. Cas9-chromatin binding information enables more accurate CRISPR off-target prediction , 2015, Nucleic acids research.
[47] Jin-Soo Kim,et al. Cas-Database: web-based genome-wide guide RNA library design for gene knockout screens using CRISPR-Cas9 , 2016, Bioinform..
[48] Neville E. Sanjana,et al. Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells , 2014, Science.
[49] R. Jaenisch,et al. One-Step Generation of Mice Carrying Reporter and Conditional Alleles by CRISPR/Cas-Mediated Genome Engineering , 2013, Cell.
[50] T. Takumi,et al. Sequence features associated with the cleavage efficiency of CRISPR/Cas9 system , 2016, Scientific Reports.
[51] Yanhui Hu,et al. Enhanced specificity and efficiency of the CRISPR/Cas9 system with optimized sgRNA parameters in Drosophila. , 2014, Cell reports.
[52] Howard M. Salis,et al. A Biophysical Model of CRISPR/Cas9 Activity for Rational Design of Genome Editing and Gene Regulation , 2016, PLoS Comput. Biol..
[53] R. Tjian,et al. Dynamics of CRISPR-Cas9 genome interrogation in living cells , 2015, Science.
[54] Yanfang Jiang,et al. Targeted activation of diverse CRISPR-Cas systems for mammalian genome editing via proximal CRISPR targeting , 2017, Nature Communications.
[55] Jennifer Doudna,et al. RNA-programmed genome editing in human cells , 2013, eLife.
[56] Xingxu Huang,et al. sgRNAcas9: A Software Package for Designing CRISPR sgRNA and Evaluating Potential Off-Target Cleavage Sites , 2014, PloS one.