Related Experiment Video

Updated: Apr 16, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

9.2K

Whole-exome sequencing increases variant detection compared to karyotyping and CMA in an unselected FGR cohort

Jianzhen Liu1, Keng Lin1, Zhuowen Mai1

  • 1Guangzhou Huadu District Maternal and Child Health Care Hospital (Hu Zhong Hospital), Guangzhou, Guangdong, China.

Scientific Reports
|April 14, 2026
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

26.6K
Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

20.7K

Related Experiment Videos

Last Updated: Apr 16, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

9.2K
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

26.6K
Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

20.7K

Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

17.0K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
17.0K

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

Characterization, evolution, and expression profiling of cotton DUF677 protein family and their potential role in drought and salt stress response.

BMC plant biology·2026

Fraxinellone suppresses inflammatory bowel disease by targeting PINK1 and activating PINK1/Parkin-mediated mitophagy.

International immunopharmacology·2026

Characterization of the Complete Mitochondrial Genome of Cricula andrei (Lepidoptera: Saturniidae) and Comparison with Other Lepidoptera Species.

Current issues in molecular biology·2026

Minimal Trade-Off and Optimal Measurement for Multiparameter Quantum Estimation.

Physical review letters·2026

Discovery and characterization of hinokiflavone as a potent natural CD137 inhibitor for Kawasaki disease.

Phytomedicine : international journal of phytotherapy and phytopharmacology·2026

Case Report: A case of advanced renal tuberculosis with recurrent "kidney stones" and specific pathological manifestations.

Frontiers in medicine·2026

Vestibular time constant and individual susceptibility to motion sickness in real-world driving.

Scientific reports·2026

Vehicle CO₂ emission prediction based on firefly with ant colony optimization tuned long short-term memory model.

Scientific reports·2026

A model predictive control-based energy management strategy for grid-connected nanogrids.

Scientific reports·2026

Plasma proteomic profiling of septic shock and acute pancreatitis identifies shared signatures and disease-specific pathways.

Scientific reports·2026

Development and validation of a predictive nomogram for cesarean delivery in term singleton pregnancies complicated by small for gestational age undergoing labor induction.

Scientific reports·2026

Search for axions and dark photons using single molecule magnets.

Scientific reports·2026

GiGCN: a network-based framework for uncovering synthetic lethal and viable genetic interactions.

Briefings in bioinformatics·2026

Comparative Genome-Wide Association Studies of Metabolites and Grain-Related Traits in Common Wheat.

Plant biotechnology journal·2026

Relationship between genetic risk, social jetlag, and obesity traits in a Turkish adult population.

Chronobiology international·2026

Molecular and histopathological evaluation of intestinal mucosal damage associated with giardiasis in naturally infected lambs.

Journal of advanced veterinary and animal research·2026

Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.

Frontiers in genetics·2026

Freely available genomic datasets for atrial fibrillation research: current resources and analytical pipeline.

Frontiers in genetics·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