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BMC Genomics
|
July 4, 2013
Identifying Mendelian disease genes with the variant effect scoring tool
Hannah Carter, Christopher Douville, Peter D Stenson, et al.
Nature Communications
|
May 18, 2021
Supervised dimensionality reduction for big data
Joshua 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 patterns
Tychele N Turner, Christopher Douville, Dewey Kim, et al.
Cancer Research
|
November 3, 2017
CRAVAT 4: Cancer-Related Analysis of Variants Toolkit
David L Masica, Christopher Douville, Collin Tokheim, et al.
Bioinformatics (Oxford, England)
|
January 18, 2013
CRAVAT: cancer-related analysis of variants toolkit
Christopher 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 cirrhosis
Hannu 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 mutation
David 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 DNA
Austin K Mattox, Beibei Yang, Christopher Douville, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 55) with videos related to
Sort By:
Page
of 6
BMC Genomics
|
July 4, 2013
Identifying Mendelian disease genes with the variant effect scoring tool
Hannah Carter, Christopher Douville, Peter D Stenson, et al.
Nature Communications
|
May 18, 2021
Supervised dimensionality reduction for big data
Joshua 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 patterns
Tychele N Turner, Christopher Douville, Dewey Kim, et al.
Cancer Research
|
November 3, 2017
CRAVAT 4: Cancer-Related Analysis of Variants Toolkit
David L Masica, Christopher Douville, Collin Tokheim, et al.
Bioinformatics (Oxford, England)
|
January 18, 2013
CRAVAT: cancer-related analysis of variants toolkit
Christopher 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 cirrhosis
Hannu 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 mutation
David 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 DNA
Austin K Mattox, Beibei Yang, Christopher Douville, et al.
Page
of 6