Multiplexed precision genome editing with trackable genomic barcodes in yeast
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Multiplexed precision genome editing with trackable genomic barcodes in yeast
Authors
Keywords
-
Journal
NATURE BIOTECHNOLOGY
Volume 36, Issue 6, Pages 512-520
Publisher
Springer Nature
Online
2018-05-08
DOI
10.1038/nbt.4137
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Evolved Cas9 variants with broad PAM compatibility and high DNA specificity
- (2018) Johnny H. Hu et al. NATURE
- A method for high‐throughput production of sequence‐verified DNA libraries and strain collections
- (2017) Justin D Smith et al. Molecular Systems Biology
- Enhanced proofreading governs CRISPR–Cas9 targeting accuracy
- (2017) Janice S. Chen et al. NATURE
- CRISPR-UMI: single-cell lineage tracing of pooled CRISPR–Cas9 screens
- (2017) Georg Michlits et al. NATURE METHODS
- High-fidelity CRISPR–Cas9 nucleases with no detectable genome-wide off-target effects
- (2016) Benjamin P. Kleinstiver et al. NATURE
- Genome-wide mapping of mutations at single-nucleotide resolution for protein, metabolic and genome engineering
- (2016) Andrew D Garst et al. NATURE BIOTECHNOLOGY
- Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9
- (2016) John G Doench et al. NATURE BIOTECHNOLOGY
- Distinct patterns of Cas9 mismatch tolerancein vitroandin vivo
- (2016) Becky X.H. Fu et al. NUCLEIC ACIDS RESEARCH
- Binding of the Fkh1 Forkhead Associated Domain to a Phosphopeptide within the Mph1 DNA Helicase Regulates Mating-Type Switching in Budding Yeast
- (2016) Antoinette M. Dummer et al. PLoS Genetics
- Rationally engineered Cas9 nucleases with improved specificity
- (2015) I. M. Slaymaker et al. SCIENCE
- Rational design of highly active sgRNAs for CRISPR-Cas9–mediated gene inactivation
- (2014) John G Doench et al. NATURE BIOTECHNOLOGY
- Selection of chromosomal DNA libraries using a multiplex CRISPR system
- (2014) Owen W Ryan et al. eLife
- DNA targeting specificity of RNA-guided Cas9 nucleases
- (2013) Patrick D Hsu et al. NATURE BIOTECHNOLOGY
- PITPs as targets for selectively interfering with phosphoinositide signaling in cells
- (2013) Aaron H Nile et al. Nature Chemical Biology
- Genome engineering in Saccharomyces cerevisiae using CRISPR-Cas systems
- (2013) James E. DiCarlo et al. NUCLEIC ACIDS RESEARCH
- Transcription termination by the eukaryotic RNA polymerase III
- (2012) Aneeshkumar G. Arimbasseri et al. Biochimica et Biophysica Acta-Gene Regulatory Mechanisms
- Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation
- (2012) Davis J. McCarthy et al. NUCLEIC ACIDS RESEARCH
- Regulation of Budding Yeast Mating-Type Switching Donor Preference by the FHA Domain of Fkh1
- (2012) Jin Li et al. PLoS Genetics
- Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications
- (2011) S. E. Polo et al. GENES & DEVELOPMENT
- SEC14 is a specific requirement for secretion of phospholipase B1 and pathogenicity of Cryptococcus neoformans
- (2011) Methee Chayakulkeeree et al. MOLECULAR MICROBIOLOGY
- Widespread occurrence of non-canonical transcription termination by human RNA polymerase III
- (2011) Andrea Orioli et al. NUCLEIC ACIDS RESEARCH
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
- (2009) M. D. Robinson et al. BIOINFORMATICS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started