Výsledky vyhledávání - Len Trigg
- Zobrazuji výsledky 1 - 7 z 7
-
1
Data mining in bioinformatics using Weka Autor Eibe Frank, Mark Hall, Len Trigg, Geoffrey Holmes, Ian H. Witten
Vydáno 2004Artigo -
2
Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials Autor 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
Vydáno 2018Pré-impressão -
3
Comparing Variant Call Files for Performance Benchmarking of Next-Generation Sequencing Variant Calling Pipelines Autor 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
Vydáno 2015Pré-impressão -
4
Joint Variant and <i>De Novo</i> Mutation Identification on Pedigrees from High-Throughput Sequencing Data Autor 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
Vydáno 2014Artigo -
5
An open resource for accurately benchmarking small variant and reference calls Autor 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
Vydáno 2019Artigo -
6
Best practices for benchmarking germline small-variant calls in human genomes Autor 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
Vydáno 2019Artigo -
7
Assessing reproducibility of inherited variants detected with short-read whole genome sequencing Autor 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
Vydáno 2022Artigo
Vyhledávací nástroje:
Související témata
Computer science
Biology
Computational biology
Gene
Genetics
Genome
Benchmarking
Business
Data mining
Marketing
Context (archaeology)
Genomics
Genotype
Paleontology
Programming language
Single-nucleotide polymorphism
Data science
Indel
1000 Genomes Project
Artificial intelligence
Benchmark (surveying)
Best practice
Bioinformatics
Botany
Cluster analysis
Computer network
Concordance
DNA sequencing
Data pre-processing
Economics