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Biorxiv : the Preprint Server for Biology
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September 26, 2025
Evaluating Language Models for Biomedical Fact-Checking: A Benchmark Dataset for Cancer Variant Interpretation Verification
Caralyn Reisle, Cameron J Grisdale, Kilannin Krysiak, et al.
Communications Biology
|
April 22, 2024
Single-cell T-cell receptor repertoire profiling in dogs
My H Hoang, Zachary L Skidmore, Hans Rindt, et al.
Genome Research
|
October 19, 2004
Systematic recovery and analysis of full-ORF human cDNA clones
Agnes Baross, Yaron S N Butterfield, Shaun M Coughlin, et al.
Nature Genetics
|
November 7, 2018
A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data
Benjamin J Ainscough, Erica K Barnell, Peter Ronning, et al.
Cell Reports
|
August 23, 2018
Oral Cavity Squamous Cell Carcinoma Xenografts Retain Complex Genotypes and Intertumor Molecular Heterogeneity
Katie M Campbell, Tianxiang Lin, Paul Zolkind, et al.
Arxiv
|
July 1, 2024
pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection
Huiming Xia, My Hoang, Evelyn Schmidt, et al.
Genome Biology
|
May 8, 2016
High-performance web services for querying gene and variant annotation
Jiwen Xin, Adam Mark, Cyrus Afrasiabi, et al.
Genome Medicine
|
November 14, 2024
pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection
Huiming Xia, My H Hoang, Evelyn Schmidt, et al.
Nature Methods
|
February 1, 2008
ALEXA: a microarray design platform for alternative expression analysis
Malachi Griffith, Michelle J Tang, Obi L Griffith, et al.
Nucleic Acids Research
|
November 5, 2015
DGIdb 2.0: mining clinically relevant drug-gene interactions
Alex H Wagner, Adam C Coffman, Benjamin J Ainscough, et al.
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of 18
Search research articles
Search
Showing results (81-90 of 175) with videos related to
Sort By:
Page
of 18
Biorxiv : the Preprint Server for Biology
|
September 26, 2025
Evaluating Language Models for Biomedical Fact-Checking: A Benchmark Dataset for Cancer Variant Interpretation Verification
Caralyn Reisle, Cameron J Grisdale, Kilannin Krysiak, et al.
Communications Biology
|
April 22, 2024
Single-cell T-cell receptor repertoire profiling in dogs
My H Hoang, Zachary L Skidmore, Hans Rindt, et al.
Genome Research
|
October 19, 2004
Systematic recovery and analysis of full-ORF human cDNA clones
Agnes Baross, Yaron S N Butterfield, Shaun M Coughlin, et al.
Nature Genetics
|
November 7, 2018
A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data
Benjamin J Ainscough, Erica K Barnell, Peter Ronning, et al.
Cell Reports
|
August 23, 2018
Oral Cavity Squamous Cell Carcinoma Xenografts Retain Complex Genotypes and Intertumor Molecular Heterogeneity
Katie M Campbell, Tianxiang Lin, Paul Zolkind, et al.
Arxiv
|
July 1, 2024
pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection
Huiming Xia, My Hoang, Evelyn Schmidt, et al.
Genome Biology
|
May 8, 2016
High-performance web services for querying gene and variant annotation
Jiwen Xin, Adam Mark, Cyrus Afrasiabi, et al.
Genome Medicine
|
November 14, 2024
pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection
Huiming Xia, My H Hoang, Evelyn Schmidt, et al.
Nature Methods
|
February 1, 2008
ALEXA: a microarray design platform for alternative expression analysis
Malachi Griffith, Michelle J Tang, Obi L Griffith, et al.
Nucleic Acids Research
|
November 5, 2015
DGIdb 2.0: mining clinically relevant drug-gene interactions
Alex H Wagner, Adam C Coffman, Benjamin J Ainscough, et al.
Page
of 18