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Mark Chaisson

Showing results (1-10 of 17) with videos related to

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Biorxiv : the Preprint Server for Biology|August 16, 2024
Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genesWalfred Ma, Mark Chaisson
Bioinformatics (Oxford, England)|April 3, 2004
Fragment assembly with short readsMark Chaisson, Pavel Pevzner, Haixu Tang
Genome Research|January 21, 2017
HySA: a Hybrid Structural variant Assembly approach using next-generation and single-molecule sequencing technologiesXian Fan, Mark Chaisson, Luay Nakhleh, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|October 18, 2011
Paired de bruijn graphs: a novel approach for incorporating mate pair information into genome assemblersPaul Medvedev, Son Pham, Mark Chaisson, et al.
Briefings in Bioinformatics|September 19, 2024
VISTA: an integrated framework for structural variant discoveryVaruni Sarwal, Seungmo Lee, Jianzhi Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2016
Assembly of long error-prone reads using de Bruijn graphsYu Lin, Jeffrey Yuan, Mikhail Kolmogorov, et al.
Bioinformatics (Oxford, England)|October 30, 2012
STAR: ultrafast universal RNA-seq alignerAlexander Dobin, Carrie A Davis, Felix Schlesinger, et al.
Genome Research|January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technologyJohn Huddleston, Swati Ranade, Maika Malig, et al.
Medrxiv : the Preprint Server for Health Sciences|September 2, 2025
Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson's diseaseFulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Brain : a Journal of Neurology|December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's diseaseFulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Biorxiv : the Preprint Server for Biology|August 16, 2024
Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genesWalfred Ma, Mark Chaisson
Bioinformatics (Oxford, England)|April 3, 2004
Fragment assembly with short readsMark Chaisson, Pavel Pevzner, Haixu Tang
Genome Research|January 21, 2017
HySA: a Hybrid Structural variant Assembly approach using next-generation and single-molecule sequencing technologiesXian Fan, Mark Chaisson, Luay Nakhleh, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|October 18, 2011
Paired de bruijn graphs: a novel approach for incorporating mate pair information into genome assemblersPaul Medvedev, Son Pham, Mark Chaisson, et al.
Briefings in Bioinformatics|September 19, 2024
VISTA: an integrated framework for structural variant discoveryVaruni Sarwal, Seungmo Lee, Jianzhi Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2016
Assembly of long error-prone reads using de Bruijn graphsYu Lin, Jeffrey Yuan, Mikhail Kolmogorov, et al.
Bioinformatics (Oxford, England)|October 30, 2012
STAR: ultrafast universal RNA-seq alignerAlexander Dobin, Carrie A Davis, Felix Schlesinger, et al.
Genome Research|January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technologyJohn Huddleston, Swati Ranade, Maika Malig, et al.
Medrxiv : the Preprint Server for Health Sciences|September 2, 2025
Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson's diseaseFulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Brain : a Journal of Neurology|December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's diseaseFulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Pageof 2