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Christopher Douville

Showing results (1-10 of 55) with videos related to

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BMC Genomics|July 4, 2013
Identifying Mendelian disease genes with the variant effect scoring toolHannah Carter, Christopher Douville, Peter D Stenson, et al.
Nature Communications|May 18, 2021
Supervised dimensionality reduction for big dataJoshua T Vogelstein, Eric W Bridgeford, Minh Tang, et al.
Human Molecular Genetics|August 7, 2015
Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patternsTychele N Turner, Christopher Douville, Dewey Kim, et al.
Cancer Research|November 3, 2017
CRAVAT 4: Cancer-Related Analysis of Variants ToolkitDavid L Masica, Christopher Douville, Collin Tokheim, et al.
Bioinformatics (Oxford, England)|January 18, 2013
CRAVAT: cancer-related analysis of variants toolkitChristopher Douville, Hannah Carter, Rick Kim, et al.
Human Mutation|October 8, 2015
Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel)Christopher Douville, David L Masica, Peter D Stenson, et al.
Scandinavian Journal of Gastroenterology|October 14, 2011
Development of a quantitative method for the diagnosis of cirrhosisHannu Huhdanpaa, Christopher Douville, Kerry Baum, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2018
Detection of aneuploidy in patients with cancer through amplification of long interspersed nucleotide elements (LINEs)Christopher Douville, Simeon Springer, Isaac Kinde, et al.
Human Genetics|August 11, 2014
Predicting survival in head and neck squamous cell carcinoma from TP53 mutationDavid L Masica, Shuli Li, Christopher Douville, et al.
Neuro-Oncology Advances|February 5, 2021
The mutational landscape of spinal chordomas and their sensitive detection using circulating tumor DNAAustin K Mattox, Beibei Yang, Christopher Douville, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
BMC Genomics|July 4, 2013
Identifying Mendelian disease genes with the variant effect scoring toolHannah Carter, Christopher Douville, Peter D Stenson, et al.
Nature Communications|May 18, 2021
Supervised dimensionality reduction for big dataJoshua T Vogelstein, Eric W Bridgeford, Minh Tang, et al.
Human Molecular Genetics|August 7, 2015
Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patternsTychele N Turner, Christopher Douville, Dewey Kim, et al.
Cancer Research|November 3, 2017
CRAVAT 4: Cancer-Related Analysis of Variants ToolkitDavid L Masica, Christopher Douville, Collin Tokheim, et al.
Bioinformatics (Oxford, England)|January 18, 2013
CRAVAT: cancer-related analysis of variants toolkitChristopher Douville, Hannah Carter, Rick Kim, et al.
Human Mutation|October 8, 2015
Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel)Christopher Douville, David L Masica, Peter D Stenson, et al.
Scandinavian Journal of Gastroenterology|October 14, 2011
Development of a quantitative method for the diagnosis of cirrhosisHannu Huhdanpaa, Christopher Douville, Kerry Baum, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2018
Detection of aneuploidy in patients with cancer through amplification of long interspersed nucleotide elements (LINEs)Christopher Douville, Simeon Springer, Isaac Kinde, et al.
Human Genetics|August 11, 2014
Predicting survival in head and neck squamous cell carcinoma from TP53 mutationDavid L Masica, Shuli Li, Christopher Douville, et al.
Neuro-Oncology Advances|February 5, 2021
The mutational landscape of spinal chordomas and their sensitive detection using circulating tumor DNAAustin K Mattox, Beibei Yang, Christopher Douville, et al.
Pageof 6