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Erika M Kvikstad

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

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Molecular Biology and Evolution|October 12, 2013
Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genomeErika M Kvikstad, Laurent Duret
Genome Research|March 12, 2010
The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are importantErika M Kvikstad, Kateryna D Makova
Genome Research|June 9, 2009
Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletionsErika M Kvikstad, Francesca Chiaromonte, Kateryna D Makova
Plos Computational Biology|October 19, 2007
A macaque's-eye view of human insertions and deletions: differences in mechanismsErika M Kvikstad, Svitlana Tyekucheva, Francesca Chiaromonte, et al.
BMC Genomics|February 3, 2018
A high throughput screen for active human transposable elementsErika M Kvikstad, Paolo Piazza, Jenny C Taylor, et al.
Advanced Genetics (Hoboken, N.J.)|July 14, 2025
Proteome-Wide Mendelian Randomization Identifies Candidate Causal Proteins for Cardiovascular DiseasesChen Li, Nicolas De Jay, Shan-Shan Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Cold Spring Harbor Molecular Case Studies|April 4, 2018
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencingAnna Schuh, Helene Dreau, Samantha J L Knight, et al.
Nature|October 4, 2023
Plasma proteomic associations with genetics and health in the UK BiobankBenjamin B Sun, Joshua Chiou, Matthew Traylor, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Pageof 1

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

Sort By:
Pageof 1
Molecular Biology and Evolution|October 12, 2013
Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genomeErika M Kvikstad, Laurent Duret
Genome Research|March 12, 2010
The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are importantErika M Kvikstad, Kateryna D Makova
Genome Research|June 9, 2009
Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletionsErika M Kvikstad, Francesca Chiaromonte, Kateryna D Makova
Plos Computational Biology|October 19, 2007
A macaque's-eye view of human insertions and deletions: differences in mechanismsErika M Kvikstad, Svitlana Tyekucheva, Francesca Chiaromonte, et al.
BMC Genomics|February 3, 2018
A high throughput screen for active human transposable elementsErika M Kvikstad, Paolo Piazza, Jenny C Taylor, et al.
Advanced Genetics (Hoboken, N.J.)|July 14, 2025
Proteome-Wide Mendelian Randomization Identifies Candidate Causal Proteins for Cardiovascular DiseasesChen Li, Nicolas De Jay, Shan-Shan Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Cold Spring Harbor Molecular Case Studies|April 4, 2018
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencingAnna Schuh, Helene Dreau, Samantha J L Knight, et al.
Nature|October 4, 2023
Plasma proteomic associations with genetics and health in the UK BiobankBenjamin B Sun, Joshua Chiou, Matthew Traylor, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Pageof 1