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Nature Biotechnology
|
February 18, 2014
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
Justin M Zook, Brad Chapman, Jason Wang, et al.
Communications Biology
|
October 13, 2024
StratoMod: predicting sequencing and variant calling errors with interpretable machine learning
Nathan Dwarshuis, Peter Tonner, Nathan D Olson, et al.
Analytical and Bioanalytical Chemistry
|
March 4, 2016
PEPR: pipelines for evaluating prokaryotic references
Nathan D Olson, Justin M Zook, Daniel V Samarov, et al.
F1000Research
|
November 11, 2017
Tools for annotation and comparison of structural variation
Fritz J Sedlazeck, Andi Dhroso, Dale L Bodian, et al.
Annals of Laboratory Medicine
|
September 1, 2016
Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships
Lisa V Kalman, Vivekananda Datta, Mickey Williams, et al.
Lab on a Chip
|
January 13, 2010
Magnetic connectors for microfluidic applications
Javier Atencia, Gregory A Cooksey, Andreas Jahn, et al.
Nature Reviews. Genetics
|
April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequences
Nathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Methods
|
June 26, 2023
Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes
Chen-Shan Chin, Sairam Behera, Asif Khalak, et al.
Genome Biology
|
June 19, 2026
Aardvark: sifting through differences in a mound of variants
James M Holt, Christopher T Saunders, Egor Dolzhenko, et al.
Genome Medicine
|
March 3, 2016
Medical implications of technical accuracy in genome sequencing
Rachel L Goldfeder, James R Priest, Justin M Zook, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 87) with videos related to
Sort By:
Page
of 9
Nature Biotechnology
|
February 18, 2014
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
Justin M Zook, Brad Chapman, Jason Wang, et al.
Communications Biology
|
October 13, 2024
StratoMod: predicting sequencing and variant calling errors with interpretable machine learning
Nathan Dwarshuis, Peter Tonner, Nathan D Olson, et al.
Analytical and Bioanalytical Chemistry
|
March 4, 2016
PEPR: pipelines for evaluating prokaryotic references
Nathan D Olson, Justin M Zook, Daniel V Samarov, et al.
F1000Research
|
November 11, 2017
Tools for annotation and comparison of structural variation
Fritz J Sedlazeck, Andi Dhroso, Dale L Bodian, et al.
Annals of Laboratory Medicine
|
September 1, 2016
Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships
Lisa V Kalman, Vivekananda Datta, Mickey Williams, et al.
Lab on a Chip
|
January 13, 2010
Magnetic connectors for microfluidic applications
Javier Atencia, Gregory A Cooksey, Andreas Jahn, et al.
Nature Reviews. Genetics
|
April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequences
Nathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Methods
|
June 26, 2023
Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes
Chen-Shan Chin, Sairam Behera, Asif Khalak, et al.
Genome Biology
|
June 19, 2026
Aardvark: sifting through differences in a mound of variants
James M Holt, Christopher T Saunders, Egor Dolzhenko, et al.
Genome Medicine
|
March 3, 2016
Medical implications of technical accuracy in genome sequencing
Rachel L Goldfeder, James R Priest, Justin M Zook, et al.
Page
of 9