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

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,...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

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...
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%...
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

Postdiagnosis Smoking Cessation and Survival Outcomes of Head and Neck Cancer Patients.

Head & neck·2025
Same author

Biomimetic Three-Arm Antifouling Coating with High Adhesion and Self-Healing Properties for Marine Optical Windows.

ACS applied materials & interfaces·2025
Same author

Application of plan-do-check-action cycle in the management of reducing surgical site infection rate of craniotomy in neurosurgery.

Neurosurgical review·2025
Same author

Artificial intelligence-large language models (AI-LLMs) for reliable and accurate cardiotocography (CTG) interpretation in obstetric practice.

Computational and structural biotechnology journal·2025
Same author

Overexpressed Rv0222 in M. smegmatis suppresses host innate immunity by downregulating miR-9 target SIRT1.

Microbial pathogenesis·2025
Same author

Significant up-regulation of Toll-like receptor (TLR) signaling pathway in Epstein-Barr virus-associated gastric cancer.

International journal of molecular epidemiology and genetics·2025

Related Experiment Video

Updated: Jul 18, 2026

Infinium Assay for Large-scale SNP Genotyping Applications
13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

Genome-wide tagging SNPs with entropy-based Monte Carlo method.

Zhenqiu Liu1, Shili Lin, Ming Tan

  • 1Division of Biostatistics, University of Maryland Greenebaum Cancer Center, Baltimore, Maryland, USA.

Journal of Computational Biology : a Journal of Computational Molecular Cell Biology
|December 7, 2006
PubMed
Summary

This study introduces a novel iterative Cross Entropy Monte Carlo (CEMC) algorithm for selecting single nucleotide polymorphisms (SNPs). The CEMC algorithm efficiently identifies informative SNPs across the entire genome without needing predefined haplotype blocks.

More Related Videos

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

Related Experiment Videos

Last Updated: Jul 18, 2026

Infinium Assay for Large-scale SNP Genotyping Applications
13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

Area of Science:

  • Genomics and Bioinformatics
  • Statistical Genetics
  • Computational Biology

Background:

  • Millions of common single nucleotide polymorphisms (SNPs) exist in the human genome, crucial for understanding complex diseases and drug responses.
  • High-throughput SNP data generation presents significant challenges for genome-wide association studies.
  • Existing SNP selection algorithms often rely on haplotype block definitions, limiting their applicability to whole-genome analyses.

Purpose of the Study:

  • To present an adaptation of the cross entropy (CE) method for efficient SNP selection.
  • To propose an iterative CE Monte Carlo (CEMC) algorithm for tagging SNP selection.
  • To develop a block-free algorithm applicable to whole-genome SNP selection.

Main Methods:

  • Developed an iterative Cross Entropy Monte Carlo (CEMC) algorithm.
  • The CEMC algorithm is independent of haplotype block structures.
  • Applied the block-free algorithm to large-scale datasets (thousands of SNPs, including simulated and real data).

Main Results:

  • Demonstrated the computational feasibility of CEMC for whole-genome SNP selection.
  • CEMC significantly outperformed random SNP selection.
  • CEMC showed superior performance compared to another block-free selection algorithm on the considered dataset.

Conclusions:

  • The proposed CEMC algorithm is a computationally feasible and effective method for whole-genome SNP selection.
  • The block-free nature of CEMC enhances its applicability across diverse genomic regions.
  • CEMC represents a significant advancement over existing SNP selection strategies.