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Justin M Zook

Showing results (21-30 of 87) with videos related to

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Nature Biotechnology|February 18, 2014
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype callsJustin M Zook, Brad Chapman, Jason Wang, et al.
Communications Biology|October 13, 2024
StratoMod: predicting sequencing and variant calling errors with interpretable machine learningNathan Dwarshuis, Peter Tonner, Nathan D Olson, et al.
Analytical and Bioanalytical Chemistry|March 4, 2016
PEPR: pipelines for evaluating prokaryotic referencesNathan D Olson, Justin M Zook, Daniel V Samarov, et al.
F1000Research|November 11, 2017
Tools for annotation and comparison of structural variationFritz J Sedlazeck, Andi Dhroso, Dale L Bodian, et al.
Annals of Laboratory Medicine|September 1, 2016
Development and Characterization of Reference Materials for Genetic Testing: Focus on Public PartnershipsLisa V Kalman, Vivekananda Datta, Mickey Williams, et al.
Lab on a Chip|January 13, 2010
Magnetic connectors for microfluidic applicationsJavier Atencia, Gregory A Cooksey, Andreas Jahn, et al.
Nature Reviews. Genetics|April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequencesNathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Methods|June 26, 2023
Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genesChen-Shan Chin, Sairam Behera, Asif Khalak, et al.
Genome Biology|June 19, 2026
Aardvark: sifting through differences in a mound of variantsJames M Holt, Christopher T Saunders, Egor Dolzhenko, et al.
Genome Medicine|March 3, 2016
Medical implications of technical accuracy in genome sequencingRachel L Goldfeder, James R Priest, Justin M Zook, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
Nature Biotechnology|February 18, 2014
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype callsJustin M Zook, Brad Chapman, Jason Wang, et al.
Communications Biology|October 13, 2024
StratoMod: predicting sequencing and variant calling errors with interpretable machine learningNathan Dwarshuis, Peter Tonner, Nathan D Olson, et al.
Analytical and Bioanalytical Chemistry|March 4, 2016
PEPR: pipelines for evaluating prokaryotic referencesNathan D Olson, Justin M Zook, Daniel V Samarov, et al.
F1000Research|November 11, 2017
Tools for annotation and comparison of structural variationFritz J Sedlazeck, Andi Dhroso, Dale L Bodian, et al.
Annals of Laboratory Medicine|September 1, 2016
Development and Characterization of Reference Materials for Genetic Testing: Focus on Public PartnershipsLisa V Kalman, Vivekananda Datta, Mickey Williams, et al.
Lab on a Chip|January 13, 2010
Magnetic connectors for microfluidic applicationsJavier Atencia, Gregory A Cooksey, Andreas Jahn, et al.
Nature Reviews. Genetics|April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequencesNathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Methods|June 26, 2023
Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genesChen-Shan Chin, Sairam Behera, Asif Khalak, et al.
Genome Biology|June 19, 2026
Aardvark: sifting through differences in a mound of variantsJames M Holt, Christopher T Saunders, Egor Dolzhenko, et al.
Genome Medicine|March 3, 2016
Medical implications of technical accuracy in genome sequencingRachel L Goldfeder, James R Priest, Justin M Zook, et al.
Pageof 9