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Cell Systems
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October 21, 2021
Democratizing long-read genome assembly
Melanie Kirsche, Michael C Schatz
Bioinformatics (Oxford, England)
|
October 27, 2020
Sapling: accelerating suffix array queries with learned data models
Melanie Kirsche, Arun Das, Michael C Schatz
Nature Methods
|
January 19, 2023
Jasmine and Iris: population-scale structural variant comparison and analysis
Melanie Kirsche, Gautam Prabhu, Rachel Sherman, et al.
Genome Biology
|
December 15, 2022
Automated assembly scaffolding using RagTag elevates a new tomato system for high-throughput genome editing
Michael Alonge, Ludivine Lebeigle, Melanie Kirsche, et al.
Genome Biology
|
December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence data
Sai Chen, Peter Krusche, Egor Dolzhenko, et al.
Genome Research
|
September 5, 2020
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing
Sergey Aganezov, Sara Goodwin, Rachel M Sherman, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 21, 2020
Genomic Diversity of SARS-CoV-2 During Early Introduction into the United States National Capital Region
Peter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
JCI Insight
|
March 22, 2021
Genomic diversity of SARS-CoV-2 during early introduction into the Baltimore-Washington metropolitan area
Peter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
Nature Communications
|
September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complex
Chen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Science (New York, N.Y.)
|
March 31, 2022
A complete reference genome improves analysis of human genetic variation
Sergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Cell Systems
|
October 21, 2021
Democratizing long-read genome assembly
Melanie Kirsche, Michael C Schatz
Bioinformatics (Oxford, England)
|
October 27, 2020
Sapling: accelerating suffix array queries with learned data models
Melanie Kirsche, Arun Das, Michael C Schatz
Nature Methods
|
January 19, 2023
Jasmine and Iris: population-scale structural variant comparison and analysis
Melanie Kirsche, Gautam Prabhu, Rachel Sherman, et al.
Genome Biology
|
December 15, 2022
Automated assembly scaffolding using RagTag elevates a new tomato system for high-throughput genome editing
Michael Alonge, Ludivine Lebeigle, Melanie Kirsche, et al.
Genome Biology
|
December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence data
Sai Chen, Peter Krusche, Egor Dolzhenko, et al.
Genome Research
|
September 5, 2020
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing
Sergey Aganezov, Sara Goodwin, Rachel M Sherman, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 21, 2020
Genomic Diversity of SARS-CoV-2 During Early Introduction into the United States National Capital Region
Peter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
JCI Insight
|
March 22, 2021
Genomic diversity of SARS-CoV-2 during early introduction into the Baltimore-Washington metropolitan area
Peter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
Nature Communications
|
September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complex
Chen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Science (New York, N.Y.)
|
March 31, 2022
A complete reference genome improves analysis of human genetic variation
Sergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Page
of 2