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James A. Gagnon

Researcher at University of Utah

Publications -  45
Citations -  5520

James A. Gagnon is an academic researcher from University of Utah. The author has contributed to research in topics: Zebrafish & CRISPR. The author has an hindex of 21, co-authored 42 publications receiving 4370 citations. Previous affiliations of James A. Gagnon include Brown University & Harvard University.

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CHOPCHOP: a CRISPR/Cas9 and TALEN web tool for genome editing

TL;DR: An online tool, CHOPCHOP, that uses efficient sequence alignment algorithms to minimize search times, and rigorously predicts off-target binding of single-guide RNAs (sgRNAs) and TALENs, making it a valuable tool for genome engineering.
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Efficient Mutagenesis by Cas9 Protein-Mediated Oligonucleotide Insertion and Large-Scale Assessment of Single-Guide RNAs

TL;DR: Improved methods and detailed protocols make Cas9-mediated mutagenesis an attractive approach for labs of all sizes and increase rates of mutagenisation by implementing several novel approaches.
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CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering

TL;DR: This major update of CHOPCHOP introduces tools for the next generation of CRISPR advances, including Cpf1 and Cas9 nickases, and provides support for custom length sgRNAs and evaluates the sequence composition of the whole sgRNA and its surrounding region using models compiled from multiple large-scale studies.
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Whole-organism lineage tracing by combinatorial and cumulative genome editing

TL;DR: It is shown that combinatorial, cumulative genome editing of a compact barcode can be used to record lineage information in multicellular systems and that rich, systematically generated maps of organismal development will advance the understanding of development in both healthy and disease states.
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Toddler: an embryonic signal that promotes cell movement via Apelin receptors.

TL;DR: Toddler is an essential, short, conserved embryonic signal that promotes cell migration during zebrafish gastrulation and helps explain previous genetic studies that found a broader requirement for APJ/Apelin receptors than for Apelin, and may be one of several uncharacterized embryonic signals.