نتائج البحث - Len Trigg

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  1. 1
    Data mining in bioinformatics using Weka

    Data mining in bioinformatics using Weka حسب Eibe Frank, Mark Hall, Len Trigg, Geoffrey Holmes, Ian H. Witten

    منشور في 2004
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  2. 2
    Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials

    Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials حسب Justin M. Zook, Jennifer McDaniel, Hemang Parikh, Haynes Heaton, Sean A. Irvine, Len Trigg, Rebecca Truty, Cory Y. McLean, Francisco M. De La Vega, Chunlin Xiao, Stephen T. Sherry, Marc Salit

    منشور في 2018
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  3. 3
    Comparing Variant Call Files for Performance Benchmarking of Next-Generation Sequencing Variant Calling Pipelines

    Comparing Variant Call Files for Performance Benchmarking of Next-Generation Sequencing Variant Calling Pipelines حسب John G. Cleary, Ross Braithwaite, Kurt Gaastra, Brian S. Hilbush, Stuart J. Inglis, Sean A. Irvine, Alan A. Jackson, Richard Littin, Mehul Rathod, David Ware, Justin M. Zook, Len Trigg, Francisco M. De La Vega

    منشور في 2015
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  4. 4
    Joint Variant and <i>De Novo</i> Mutation Identification on Pedigrees from High-Throughput Sequencing Data

    Joint Variant and <i>De Novo</i> Mutation Identification on Pedigrees from High-Throughput Sequencing Data حسب John G. Cleary, Ross Braithwaite, Kurt Gaastra, Brian S. Hilbush, Stuart J. Inglis, Sean A. Irvine, Alan A. Jackson, Richard Littin, Sahar Nohzadeh‐Malakshah, Mehul Rathod, David Ware, Len Trigg, Francisco M. De La Vega

    منشور في 2014
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  5. 5
    An open resource for accurately benchmarking small variant and reference calls

    An open resource for accurately benchmarking small variant and reference calls حسب Justin M. Zook, Jennifer McDaniel, Nathan D. Olson, Justin Wagner, Hemang Parikh, Haynes Heaton, Sean A. Irvine, Len Trigg, Rebecca Truty, Cory Y. McLean, Francisco M. De La Vega, Chunlin Xiao, Stephen T. Sherry, Marc Salit

    منشور في 2019
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  6. 6
    Best practices for benchmarking germline small-variant calls in human genomes

    Best practices for benchmarking germline small-variant calls in human genomes حسب Peter Krusche, Len Trigg, Paul C. Boutros, Christopher E. Mason, Francisco M. De La Vega, Benjamin L. Moore, Mar González-Porta, Michael A. Eberle, Živana Težak, Samir Lababidi, Rebecca Truty, George Asimenos, Birgit Funke, Mark Fleharty, Brad Chapman, Marc Salit, Justin M. Zook

    منشور في 2019
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  7. 7
    Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

    Assessing reproducibility of inherited variants detected with short-read whole genome sequencing حسب Bohu Pan, Luyao Ren, Vitor Onuchic, Meijian Guan, Rebecca Kusko, Steve Bruinsma, Len Trigg, Andreas Scherer, Baitang Ning, Chaoyang Zhang, Christine Glidewell-Kenney, Chunlin Xiao, Eric Donaldson, Fritz J. Sedlazeck, Gary P. Schroth, Gökhan Yavaş, Haiying Grunenwald, Haodong Chen, Heather Meinholz, Joe Meehan, Jing Wang, Jingcheng Yang, Jonathan Foox, Jun Shang, Kelci Miclaus, Lianhua Dong, Leming Shi, Marghoob Mohiyuddin, Mehdi Pirooznia, Ping Gong, Rooz Golshani, Russ Wolfinger, Samir Lababidi, Sayed Mohammad Ebrahim Sahraeian, Stephen T. Sherry, Tao Han, Tao Chen, Tieliu Shi, Wanwan Hou, Weigong Ge, Wen Zou, Wenjing Guo, Wenjun Bao, Wenzhong Xiao, Xiaohui Fan, Yoichi Gondo, Ying Yu, Yongmei Zhao, Zhenqiang Su, Zhichao Liu, Weida Tong, Wenming Xiao, Justin M. Zook, Yuanting Zheng, Huixiao Hong

    منشور في 2022
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