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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.
Genome Research
|
August 6, 2011
Synthetic spike-in standards for RNA-seq experiments
Lichun Jiang, Felix Schlesinger, Carrie A Davis, et al.
BMC Biotechnology
|
March 21, 2018
Cell-based reference samples designed with specific differences in microRNA biomarkers
P Scott Pine, Steven P Lund, Sanford A Stass, et al.
Nucleic Acids Research
|
March 24, 2017
Measurements of translation initiation from all 64 codons in E. coli
Ariel Hecht, Jeff Glasgow, Paul R Jaschke, 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.
Nature
|
March 3, 2006
Top-down standards will not serve systems biology
John Quackenbush, Christian Stoeckert, Catherine Ball, et al.
Nature Methods
|
July 18, 2017
Genome-wide reconstruction of complex structural variants using read clouds
Noah Spies, Ziming Weng, Alex Bishara, et al.
Nature
|
June 21, 2023
Single-cell quantification of ribosome occupancy in early mouse development
Hakan Ozadam, Tori Tonn, Crystal M Han, et al.
BMC Genomics
|
January 17, 2016
svclassify: a method to establish benchmark structural variant calls
Hemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
The Journal of Molecular Diagnostics : JMD
|
January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing
Stephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
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.
Genome Research
|
August 6, 2011
Synthetic spike-in standards for RNA-seq experiments
Lichun Jiang, Felix Schlesinger, Carrie A Davis, et al.
BMC Biotechnology
|
March 21, 2018
Cell-based reference samples designed with specific differences in microRNA biomarkers
P Scott Pine, Steven P Lund, Sanford A Stass, et al.
Nucleic Acids Research
|
March 24, 2017
Measurements of translation initiation from all 64 codons in E. coli
Ariel Hecht, Jeff Glasgow, Paul R Jaschke, 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.
Nature
|
March 3, 2006
Top-down standards will not serve systems biology
John Quackenbush, Christian Stoeckert, Catherine Ball, et al.
Nature Methods
|
July 18, 2017
Genome-wide reconstruction of complex structural variants using read clouds
Noah Spies, Ziming Weng, Alex Bishara, et al.
Nature
|
June 21, 2023
Single-cell quantification of ribosome occupancy in early mouse development
Hakan Ozadam, Tori Tonn, Crystal M Han, et al.
BMC Genomics
|
January 17, 2016
svclassify: a method to establish benchmark structural variant calls
Hemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
The Journal of Molecular Diagnostics : JMD
|
January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing
Stephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Page
of 6