Related Experiment Video

Updated: Dec 14, 2025

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
11:02

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

Published on: October 18, 2013

19.8K

Author Correction: A robust benchmark for detection of germline large deletions and insertions

Justin M Zook1, Nancy F Hansen2, Nathan D Olson3

  • 1Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD, USA. jzook@nist.gov.

Nature Biotechnology
|July 24, 2020
PubMed

Abstract:

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

More Related Videos

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
09:40

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9

Published on: January 3, 2015

96.3K
An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants
09:32

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants

Published on: November 8, 2017

8.1K

Related Experiment Videos

Last Updated: Dec 14, 2025

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
11:02

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

Published on: October 18, 2013

19.8K
Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
09:40

Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9

Published on: January 3, 2015

96.3K
An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants
09:32

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants

Published on: November 8, 2017

8.1K

Related Concept Videos

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

18.4K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.4K

Articles linked to this work by shared authors, journal, and citation graph.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

De Bruijn graphs for pangenomics: in-depth performance benchmarking of de Bruijn graph-based tools for read mapping.

Briefings in bioinformatics·2026

The Endoterpenoid System: A Membrane-Based Logic Framework for Integrating Cannabinoid, Olfactory, and Lipid-Sensitive Receptor Crosstalk.

Journal of neuroscience research·2026

A Comparison of Machine Learning and Human Graders for Glaucoma Diagnosis from Fundus Images for Population Screening.

Ophthalmology·2026

A complete diploid human genome benchmark for personalized genomics.

Cell·2026

Long-term major histocompatibility complex class I suppression in astronauts and clinical implications.

Communications biology·2026

Precise genomic integration of large DNA fragments by donor-directed annealing using prime editing.

Nature biotechnology·2026

Donor-complementary prime editing enables precise kilobase and library-compatible DNA insertions.

Nature biotechnology·2026

Megascale microbiome analysis with DartUniFrac.

Nature biotechnology·2026

Engineered bacterial siderophore production accelerates rock weathering for carbon removal.

Nature biotechnology·2026

Transferable genetic toolsets for nonmodel gut Clostridia enable in vivo reversible control of metabolite production.

Nature biotechnology·2026

Adaptive model-guided protein evolution with sparse data optimizes compact eukaryotic genome editors.

Nature biotechnology·2026

A data collection of UML diagrams in PlantUML notation mined from open-source software.

Data in brief·2026

In Science Journals.

Science (New York, N.Y.)·2026

Lateral Extra-articular Tenodesis Internet Search Trends Correlate to the Quantity of Publications From 2020 to 2024.

Arthroscopy, sports medicine, and rehabilitation·2026

In Science Journals.

Science (New York, N.Y.)·2026

In Science Journals.

Science (New York, N.Y.)·2026

Decision making in macromolecular crystallography: how to be a productive structural biologist.

Acta crystallographica. Section D, Structural biology·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us