Pooled clone collections by multiplexed CRISPR-Cas12a-assisted gene tagging in yeast
暂无分享,去创建一个
[1] Krisztina Gubicza,et al. CRISPR/Cas12a-assisted PCR tagging of mammalian genes , 2018, bioRxiv.
[2] Benjamin Dubreuil,et al. YeastRGB: comparing the abundance and localization of yeast proteins across cells and libraries , 2018, Nucleic Acids Res..
[3] Fumihito Arai,et al. Intelligent Image-Activated Cell Sorting , 2018, Cell.
[4] E. Levy,et al. Genome-wide C-SWAT library for high-throughput yeast genome tagging , 2018, Nature Methods.
[5] Anton Khmelinskii,et al. Mapping Degradation Signals and Pathways in a Eukaryotic N-terminome. , 2018, Molecular cell.
[6] James E. DiCarlo,et al. High-throughput creation and functional profiling of DNA sequence variant libraries using CRISPR/Cas9 in yeast , 2018, Nature Biotechnology.
[7] Attila Balint,et al. Systematic analysis of complex genetic interactions , 2018, Science.
[8] Robert P. St.Onge,et al. Multiplexed precision genome editing with trackable genomic barcodes in yeast , 2018, Nature Biotechnology.
[9] Anastasia Baryshnikova,et al. Unification of Protein Abundance Datasets Yields a Quantitative Saccharomyces cerevisiae Proteome. , 2018, Cell systems.
[10] Johannes A. Roubos,et al. CRISPR/Cpf1 enables fast and simple genome editing of Saccharomyces cerevisiae , 2017, Yeast.
[11] Jean-Marc Daran,et al. FnCpf1: a novel and efficient genome editing tool for Saccharomyces cerevisiae , 2017, Nucleic acids research.
[12] Márton Hunyadi,et al. National Academies of Sciences, Engineering, and Medicine (2015) The Integration of Immigrants into American Society. Washington, DC: The National Academies Press. 458 pages , 2017 .
[13] P. Billon,et al. CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons. , 2017, Molecular cell.
[14] Junhao Fu,et al. A ‘new lease of life’: FnCpf1 possesses DNA cleavage activity for genome editing in human cells , 2017, Nucleic acids research.
[15] Heng Li,et al. Minimap2: pairwise alignment for nucleotide sequences , 2017, Bioinform..
[16] S. Kosuri,et al. Highly parallel genome variant engineering with CRISPR/Cas9 , 2018, Nature Genetics.
[17] Mazhar Adli,et al. CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations , 2017, Nature Methods.
[18] J. Haber,et al. Rad51-mediated double-strand break repair and mismatch correction of divergent substrates , 2017, Nature.
[19] Sasha F. Levy,et al. A method for high‐throughput production of sequence‐verified DNA libraries and strain collections , 2017, Molecular systems biology.
[20] Jin-Wu Nam,et al. In vivo high-throughput profiling of CRISPR–Cpf1 activity , 2016, Nature Methods.
[21] Ryan T Gill,et al. Genome-wide mapping of mutations at single-nucleotide resolution for protein, metabolic and genome engineering , 2016, Nature Biotechnology.
[22] Division on Earth. Gene Drives on the Horizon , 2016 .
[23] A. Heger,et al. UMI-tools: modeling sequencing errors in Unique Molecular Identifiers to improve quantification accuracy , 2016, bioRxiv.
[24] Paul J. McMurdie,et al. DADA2: High resolution sample inference from Illumina amplicon data , 2016, Nature Methods.
[25] Matthias Meurer,et al. One library to make them all: streamlining the creation of yeast libraries via a SWAp-Tag strategy , 2016, Nature Methods.
[26] David Baker,et al. Multiplex pairwise assembly of array-derived DNA oligonucleotides , 2015, Nucleic acids research.
[27] James E. DiCarlo,et al. Safeguarding CRISPR-Cas9 gene drives in yeast , 2015, Nature Biotechnology.
[28] A. Regev,et al. Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System , 2015, Cell.
[29] W. Huber,et al. Protein quality control at the inner nuclear membrane , 2014, Nature.
[30] Paul Theodor Pyl,et al. HTSeq—a Python framework to work with high-throughput sequencing data , 2014, bioRxiv.
[31] Peter Rodgers,et al. eulerAPE: Drawing Area-Proportional 3-Venn Diagrams Using Ellipses , 2014, PloS one.
[32] G. Church,et al. Large-scale de novo DNA synthesis: technologies and applications , 2014, Nature Methods.
[33] Shiyou Zhu,et al. High-throughput screening of a CRISPR/Cas9 library for functional genomics in human cells , 2014, Nature.
[34] Neville E. Sanjana,et al. Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells , 2014, Science.
[35] Edith D. Wong,et al. The Reference Genome Sequence of Saccharomyces cerevisiae: Then and Now , 2013, G3: Genes, Genomes, Genetics.
[36] Michael W. Davidson,et al. A bright monomeric green fluorescent protein derived from Branchiostoma lanceolatum , 2013, Nature Methods.
[37] Richard J Maraia,et al. Transcription termination by the eukaryotic RNA polymerase III. , 2013, Biochimica et biophysica acta.
[38] L. Steinmetz,et al. Genotyping 1000 yeast strains by next-generation sequencing , 2013, BMC Genomics.
[39] Brenda J. Andrews,et al. Functional Analysis With a Barcoder Yeast Gene Overexpression System , 2012, G3: Genes | Genomes | Genetics.
[40] Natasha S. Barteneva,et al. Imaging Flow Cytometry , 2016, Methods in Molecular Biology.
[41] Philipp J. Keller,et al. Tandem fluorescent protein timers for in vivo analysis of protein dynamics , 2012, Nature Biotechnology.
[42] Steven L Salzberg,et al. Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.
[43] S. Linnarsson,et al. Counting absolute numbers of molecules using unique molecular identifiers , 2011, Nature Methods.
[44] M. Mann,et al. Comprehensive mass-spectrometry-based proteome quantification of haploid versus diploid yeast , 2008, Nature.
[45] U. K. Laemmli,et al. The anchor-away technique: rapid, conditional establishment of yeast mutant phenotypes. , 2008, Molecular cell.
[46] C. Landry,et al. An in Vivo Map of the Yeast Protein Interactome , 2008, Science.
[47] E. O’Shea,et al. Quantification of protein half-lives in the budding yeast proteome , 2006, Proceedings of the National Academy of Sciences.
[48] J. Derisi,et al. Single-cell proteomic analysis of S. cerevisiae reveals the architecture of biological noise , 2006, Nature.
[49] Sean R. Collins,et al. Global landscape of protein complexes in the yeast Saccharomyces cerevisiae , 2006, Nature.
[50] T. Hughes,et al. Mapping pathways and phenotypes by systematic gene overexpression. , 2006, Molecular cell.
[51] Simon Kasif,et al. GC/AT-content spikes as genomic punctuation marks. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[52] Michael Knop,et al. A versatile toolbox for PCR‐based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes , 2004, Yeast.
[53] K. Thorn,et al. Optimized cassettes for fluorescent protein tagging in Saccharomyces cerevisiae , 2004, Yeast.
[54] E. O’Shea,et al. Global analysis of protein expression in yeast , 2003, Nature.
[55] E. O’Shea,et al. Global analysis of protein localization in budding yeast , 2003, Nature.
[56] Chang‐Deng Hu,et al. Visualization of interactions among bZIP and Rel family proteins in living cells using bimolecular fluorescence complementation. , 2002, Molecular cell.
[57] P. Bork,et al. Functional organization of the yeast proteome by systematic analysis of protein complexes , 2002, Nature.
[58] Gary D Bader,et al. Systematic Genetic Analysis with Ordered Arrays of Yeast Deletion Mutants , 2001, Science.
[59] K. Siegers,et al. Epitope tagging of yeast genes using a PCR‐based strategy: more tags and improved practical routines , 1999, Yeast.
[60] P. Philippsen,et al. Saccharomyces cerevisiae cells with defective spindle pole body outer plaques accomplish nuclear migration via half-bridge-organized microtubules. , 1998, Molecular biology of the cell.
[61] Fred Winston,et al. Construction of a set of convenient saccharomyces cerevisiae strains that are isogenic to S288C , 1995, Yeast.
[62] O. Ozier-Kalogeropoulos,et al. A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae. , 1993, Nucleic acids research.
[63] M. Johnston. A model fungal gene regulatory mechanism: the GAL genes of Saccharomyces cerevisiae. , 1987, Microbiological reviews.
[64] J W Szostak,et al. Yeast transformation: a model system for the study of recombination. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[65] Anton Khmelinskii,et al. Analysis of protein dynamics with tandem fluorescent protein timers. , 2014, Methods in molecular biology.
[66] Corey Nislow,et al. Bugs, drugs and chemical genomics. , 2011, Nature chemical biology.
[67] Y. Shiio,et al. Epitope tagging. , 1995, Methods in enzymology.