VideoCategory: Gene mapping

Star icon

Gene mapping is a critical area within genetics focused on identifying the locations and relationships of genes within genomes. This research helps scientists understand hereditary traits, genetic disorders, and evolutionary biology. It forms a foundational pillar in biological sciences, enabling insights into gene function and interaction. JoVE Visualize enhances access to gene mapping research by pairing PubMed articles with JoVE experiment videos, providing researchers and students a richer comprehension of experimental approaches and genetic findings.

Key Methods & Emerging Trends

Core Gene Mapping Methods

Classic gene mapping techniques include linkage analysis, which uses genetic markers to track inheritance patterns within families, and physical mapping methods that determine gene locations on chromosomes. Cytogenetic mapping visualizes gene positions using microscopy, while molecular approaches such as restriction fragment length polymorphism (RFLP) and single nucleotide polymorphism (SNP) tracking offer precise gene localization. These methods remain fundamental for constructing gene mapping diagrams and developing understanding of gene interactions in humans and other organisms.

Emerging and Innovative Approaches

Recent advances integrate high-throughput sequencing and bioinformatics to refine gene mapping resolution. Techniques like whole-genome sequencing and genome-wide association studies (GWAS) enable identification of genetic variants linked to complex traits and diseases. Emerging CRISPR-based mapping and optical mapping technologies provide innovative ways to analyze structural variations and gene functions. These approaches are expanding the scope of gene mapping research, allowing more detailed gene mapping examples and facilitating novel types of gene mapping beyond traditional strategies.

Research

Fields in

VideoCategory: Gene mapping

Recently Published Articles

August 9, 2019

|

JIMD Reports

Prevalence of Fabry disease in male dialysis patients: Argentinean screening study

  • Joaquín Frabasil, Consuelo Durand, Silvia Sokn et al.

December 20, 2018

|

The Journal of Dermatology

G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome

  • Ming-Xing Xie, Wei-Ping Yang, Hao-Jie Luo et al.

August 27, 2020

|

Genes

Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss

  • Saba Zafar, Mohsin Shahzad, Rafaqat Ishaq et al.

December 4, 2020

|

Human Molecular Genetics

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

  • Ella M M A Martin, Annabelle Enriquez, Duncan B Sparrow et al.

August 17, 2021

|

Endocrinology

Leptin Receptor Expression in GABAergic Cells is Not Sufficient to Normalize Metabolism and Reproduction in Mice

  • Paula G F Quaresma, Frederick Wasinski, Naira S Mansano et al.

September 24, 2021

|

Pediatric Blood & Cancer

Potential benefits of rapid genetic testing for germline WT1 in infants with bilateral renal tumors: A case report

  • Haruna Yoshikawa, Takeshi Sato, Takahiro Ishikawa et al.

August 16, 2014

|

American Journal of Medical Genetics. Part A

A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome

  • Deirdre Máire Seoighe, Veselina Gadancheva, Regina Regan et al.

March 16, 2012

|

European Journal of Human Genetics : EJHG

A family-based association test to detect gene-gene interactions in the presence of linkage

  • Lizzy De Lobel, Lutgarde Thijs, Tatiana Kouznetsova et al.