Rapidly evolving homing CRISPR barcodes

Nature Methods

Volumn 14, Issue 2, 2017, Pages 195-200

  Kalhor, Reza ^a   Mali, Prashant ^b   Church, George M ^a,c  

^a HARVARD MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^c HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; RNA 16S; BACTERIAL PROTEIN; CAS9 ENDONUCLEASE STREPTOCOCCUS PYOGENES; ENDONUCLEASE; GREEN FLUORESCENT PROTEIN; GUIDE RNA;

AMPLICON; ARTICLE; CELL POPULATION; CELL VIABILITY; CLONAL CELL LINE; CONNECTOME; CONTROLLED STUDY; CRISPR CAS SYSTEM; DNA BARCODING; DNA END JOINING REPAIR; EMBRYO; ENTROPY; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN CELL; INDUCED MUTATION; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; RNA TRANSCRIPTION; STREPTOCOCCUS PYOGENES; CLUSTERED REGULARLY INTERSPACED SHORT PALINDROMIC REPEAT; GENE VECTOR; GENETICS; HEK293 CELL LINE; HIGH THROUGHPUT SEQUENCING; LENTIVIRINAE; METABOLISM; PROCEDURES;

BACTERIAL PROTEINS; CLUSTERED REGULARLY INTERSPACED SHORT PALINDROMIC REPEATS; CRISPR-CAS SYSTEMS; ENDONUCLEASES; GENETIC VECTORS; GREEN FLUORESCENT PROTEINS; HEK293 CELLS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; LENTIVIRUS; RNA, GUIDE;

EID: 85002263454     PISSN: 15487091     EISSN: 15487105     Source Type: Journal    
DOI: 10.1038/nmeth.4108     Document Type: Article

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