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Len Trigg

Showing results (1-10 of 6) with videos related to

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Bioinformatics (Oxford, England)|April 10, 2004
Data mining in bioinformatics using WekaEibe Frank, Mark Hall, Len Trigg, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|May 31, 2014
Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing dataJohn G Cleary, Ross Braithwaite, Kurt Gaastra, et al.
Nature Biotechnology|April 3, 2019
An open resource for accurately benchmarking small variant and reference callsJustin M Zook, Jennifer McDaniel, Nathan D Olson, et al.
Nature Biotechnology|March 13, 2019
Best practices for benchmarking germline small-variant calls in human genomesPeter Krusche, Len Trigg, Paul C Boutros, et al.
Nature Biotechnology|March 23, 2019
Author Correction: Best practices for benchmarking germline small-variant calls in human genomesPeter Krusche, Len Trigg, Paul C Boutros, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|April 10, 2004
Data mining in bioinformatics using WekaEibe Frank, Mark Hall, Len Trigg, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|May 31, 2014
Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing dataJohn G Cleary, Ross Braithwaite, Kurt Gaastra, et al.
Nature Biotechnology|April 3, 2019
An open resource for accurately benchmarking small variant and reference callsJustin M Zook, Jennifer McDaniel, Nathan D Olson, et al.
Nature Biotechnology|March 13, 2019
Best practices for benchmarking germline small-variant calls in human genomesPeter Krusche, Len Trigg, Paul C Boutros, et al.
Nature Biotechnology|March 23, 2019
Author Correction: Best practices for benchmarking germline small-variant calls in human genomesPeter Krusche, Len Trigg, Paul C Boutros, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
Pageof 1