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Melanie Kirsche

Showing results (1-10 of 15) with videos related to

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Cell Systems|October 21, 2021
Democratizing long-read genome assemblyMelanie Kirsche, Michael C Schatz
Bioinformatics (Oxford, England)|October 27, 2020
Sapling: accelerating suffix array queries with learned data modelsMelanie Kirsche, Arun Das, Michael C Schatz
Nature Methods|January 19, 2023
Jasmine and Iris: population-scale structural variant comparison and analysisMelanie 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 editingMichael Alonge, Ludivine Lebeigle, Melanie Kirsche, et al.
Genome Biology|December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence dataSai Chen, Peter Krusche, Egor Dolzhenko, et al.
Genome Research|September 5, 2020
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencingSergey 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 RegionPeter 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 areaPeter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-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 variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Cell Systems|October 21, 2021
Democratizing long-read genome assemblyMelanie Kirsche, Michael C Schatz
Bioinformatics (Oxford, England)|October 27, 2020
Sapling: accelerating suffix array queries with learned data modelsMelanie Kirsche, Arun Das, Michael C Schatz
Nature Methods|January 19, 2023
Jasmine and Iris: population-scale structural variant comparison and analysisMelanie 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 editingMichael Alonge, Ludivine Lebeigle, Melanie Kirsche, et al.
Genome Biology|December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence dataSai Chen, Peter Krusche, Egor Dolzhenko, et al.
Genome Research|September 5, 2020
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencingSergey 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 RegionPeter 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 areaPeter M Thielen, Shirlee Wohl, Thomas Mehoke, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-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 variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Pageof 2