Jove
Visualize
Contact Us
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

Related Concept Videos

Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

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%...
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Modern Molecular Taxonomy01:29

Modern Molecular Taxonomy

Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...

You might also read

Related Articles

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

Sort by
Same author

Unlocking almond breeding for nutritional composition with hyperspectral imaging.

Plant phenomics (Washington, D.C.)·2026
Same author

How hyperoxia affects systemic redox state: insights from PULSE-Ox, a randomised double-blind mechanistic feasibility trial.

BJA open·2026
Same author

Identification of QTLs linked to bioactive flavonoids and glycosides in the apricot fruit (Prunus armeniaca L.).

BMC genomics·2026
Same author

Both conventionally and organically fertilized tomatoes maintain fruit quality through uncontrolled green peach aphid infestation, with a transcriptional shift towards catabolism.

PloS one·2026
Same author

Characterising the clinical associations of hallucinogen persisting perception disorder: a retrospective cohort study.

Translational psychiatry·2026
Same author

Genetic evaluation of flowering, maturity time and productivity in almond (Prunus dulcis): heritability estimates and breeding value predictions.

BMC plant biology·2026

Related Experiment Video

Updated: May 10, 2026

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations
08:03

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations

Published on: December 7, 2021

Comparative genomics analysis in Prunoideae to identify biologically relevant polymorphisms.

Tyson Koepke1, Scott Schaeffer, Artemus Harper

  • 1Department of Horticulture, Washington State University, Pullman, WA, USA; Molecular Plant Sciences Graduate Program, Washington State University, Pullman, WA, USA.

Plant Biotechnology Journal
|June 15, 2013
PubMed
Summary

Comparative genomics in Prunus species revealed millions of single nucleotide polymorphisms (SNPs). Non-sense SNPs were linked to specific gene functions, potentially explaining traits like sweet cherry

Keywords:
PrunusRosaceaeSNPsfruit ripeninggenomicsmissense mutations

More Related Videos

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

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
14:06

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Published on: June 23, 2012

Related Experiment Videos

Last Updated: May 10, 2026

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations
08:03

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations

Published on: December 7, 2021

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

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
14:06

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Published on: June 23, 2012

Area of Science:

  • Plant genomics
  • Comparative genomics
  • Population genetics

Background:

  • The genus Prunus, encompassing economically significant species like peach, almond, and sweet cherry, exhibits substantial physiological and biological diversity.
  • Understanding genetic variations within Prunus is crucial for crop improvement and understanding evolutionary relationships.

Purpose of the Study:

  • To conduct a comparative genomic analysis of almond and sweet cherry using the peach genome as a reference.
  • To identify and characterize single nucleotide polymorphisms (SNPs), particularly non-sense mutations, and investigate their distribution and potential functional implications across Prunus species.

Main Methods:

  • Whole-genome sequencing of four almond accessions and one sweet cherry cultivar.
  • Reference-based mapping of sequencing reads to the peach genome.
  • Identification and analysis of single nucleotide polymorphisms (SNPs).
  • Gene Ontology (GO) enrichment analysis using Blast2GO for non-sense SNPs.

Main Results:

  • Millions of single nucleotide polymorphisms (SNPs) were identified across the analyzed Prunus species.
  • Approximately 70,000 non-sense mutations were found among the 13 million identified SNPs.
  • Non-sense SNPs were not uniformly distributed across gene ontology terms, with specific enrichment in 1-aminocyclopropane-1-carboxylate synthase (ACS) and 1-aminocyclopropane-1-carboxylate oxidase (ACO) genes in sweet cherry.
  • Candidate genes associated with almond bitterness were identified through sequence comparison.

Conclusions:

  • The study provides a comprehensive genomic comparison within the Prunus genus, highlighting significant SNP diversity.
  • Non-sense SNP abundance and their distribution across specific gene functions offer insights into species-specific traits, such as the non-climacteric ripening of sweet cherry.
  • This research pioneers the link between non-sense SNP abundance and specific Gene Ontology terms in plants, offering a novel perspective for functional genomics.