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M Wenger

Showing results (141-150 of 166) with videos related to

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Genome Research|March 24, 2012
Coding exons function as tissue-specific enhancers of nearby genesRamon Y Birnbaum, E Josephine Clowney, Orly Agamy, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
A computational model for quantifying instability of tandem repeats across the genomeEgor Dolzhenko, Adam English, Tom Mokveld, et al.
Nature Biotechnology|September 1, 2022
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformerGunjan Baid, Daniel E Cook, Kishwar Shafin, et al.
Leukemia|June 22, 2013
Prediction of poor outcome in CLL patients following first-line treatment with fludarabine, cyclophosphamide and rituximabA M Fink, S Böttcher, M Ritgen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
Annals of Human Genetics|November 12, 2019
Improved assembly and variant detection of a haploid human genome using single-molecule, high-fidelity long readsMitchell R Vollger, Glennis A Logsdon, Peter A Audano, et al.
Clinical Epigenetics|November 14, 2021
Father-to-offspring transmission of extremely long NOTCH2NLC repeat expansions with contractions: genetic and epigenetic profiling with long-read sequencingHiromi Fukuda, Daisuke Yamaguchi, Kristofor Nyquist, et al.
Cell Genomics|February 13, 2023
A multi-platform reference for somatic structural variation detectionJose Espejo Valle-Inclan, Nicolle J M Besselink, Ewart de Bruijn, et al.
Plos Computational Biology|June 20, 2020
A crowdsourced set of curated structural variants for the human genomeLesley M Chapman, Noah Spies, Patrick Pai, et al.
Nature Communications|May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohortWarren A Cheung, Adam F Johnson, William J Rowell, et al.
Pageof 17

Showing results (141-150 of 166) with videos related to

Sort By:
Pageof 17
Genome Research|March 24, 2012
Coding exons function as tissue-specific enhancers of nearby genesRamon Y Birnbaum, E Josephine Clowney, Orly Agamy, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
A computational model for quantifying instability of tandem repeats across the genomeEgor Dolzhenko, Adam English, Tom Mokveld, et al.
Nature Biotechnology|September 1, 2022
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformerGunjan Baid, Daniel E Cook, Kishwar Shafin, et al.
Leukemia|June 22, 2013
Prediction of poor outcome in CLL patients following first-line treatment with fludarabine, cyclophosphamide and rituximabA M Fink, S Böttcher, M Ritgen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
Annals of Human Genetics|November 12, 2019
Improved assembly and variant detection of a haploid human genome using single-molecule, high-fidelity long readsMitchell R Vollger, Glennis A Logsdon, Peter A Audano, et al.
Clinical Epigenetics|November 14, 2021
Father-to-offspring transmission of extremely long NOTCH2NLC repeat expansions with contractions: genetic and epigenetic profiling with long-read sequencingHiromi Fukuda, Daisuke Yamaguchi, Kristofor Nyquist, et al.
Cell Genomics|February 13, 2023
A multi-platform reference for somatic structural variation detectionJose Espejo Valle-Inclan, Nicolle J M Besselink, Ewart de Bruijn, et al.
Plos Computational Biology|June 20, 2020
A crowdsourced set of curated structural variants for the human genomeLesley M Chapman, Noah Spies, Patrick Pai, et al.
Nature Communications|May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohortWarren A Cheung, Adam F Johnson, William J Rowell, et al.
Pageof 17