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Related Concept Videos

Genetic Screens02:46

Genetic Screens

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Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
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Single Nucleotide Polymorphisms-SNPs01:05

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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,...
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Randomized Experiments01:13

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The randomization process involves assigning study participants randomly to experimental or control groups based on their probability of being equally assigned. Randomization is meant to eliminate selection bias and balance known and unknown confounding factors so that the control group is similar to the treatment group as much as possible. A computer program and a random number generator can be used to assign participants to groups in a way that minimizes bias.
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Regression Toward the Mean01:52

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Regression toward the mean (“RTM”) is a phenomenon in which extremely high or low values—for example, and individual’s blood pressure at a particular moment—appear closer to a group’s average upon remeasuring. Although this statistical peculiarity is the result of random error and chance, it has been problematic across various medical, scientific, financial and psychological applications. In particular, RTM, if not taken into account, can interfere when...
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Incomplete Dominance01:43

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Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
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Behavior genetics explores how genetic inheritance influences human behavior. It focuses on how genes, passed from parents to offspring, contribute to the development of behavioral traits and tendencies. This branch of genetics seeks to understand the complex interplay between inherited genetic factors and environmental influences in shaping our behaviors.
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Updated: Feb 17, 2026

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Recent Developments in Mendelian Randomization Studies.

Jie Zheng1, Denis Baird1, Maria-Carolina Borges1

  • 1MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, UK.

Current Epidemiology Reports
|December 12, 2017
PubMed
Summary
This summary is machine-generated.

Mendelian randomization (MR) uses genetic variants to assess causality in observational studies, offering insights where randomized trials are infeasible. Careful interpretation is key to avoid errors in this powerful epidemiological tool.

Keywords:
Databases and automation tools for causal inferenceDisease progressionDrug developmentHypothesis-free causalityMendelian randomization

Related Experiment Videos

Last Updated: Feb 17, 2026

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

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Area of Science:

  • Epidemiology
  • Genetics
  • Biostatistics

Background:

  • Mendelian randomization (MR) is a causal inference technique for observational studies.
  • It leverages genetic variants, which are less prone to confounding and reverse causation due to Mendelian inheritance.
  • MR provides a powerful alternative for causal assessment when randomized controlled trials are not feasible.

Purpose of the Study:

  • To review the fundamental principles, assumptions, and limitations of Mendelian randomization.
  • To discuss advanced MR methodologies and their applications.
  • To highlight the growing potential of MR in biological and omics research.

Main Methods:

  • Review of Mendelian randomization principles and statistical foundations.
  • Discussion of extensions: two-sample MR, bidirectional MR, multivariable MR, and factorial MR.
  • Exploration of recent developments including automation (MR-Base) and phenome-wide MR.

Main Results:

  • MR methodology offers robust causal inference in complex biological networks.
  • Recent advancements enhance automation and broaden applicability.
  • The technique is increasingly informing drug development and disease prevention strategies.

Conclusions:

  • Mendelian randomization is a valuable tool for establishing causality in observational data.
  • Its utility is amplified by large genomic databases and methodological advancements.
  • MR will play a crucial role in future biological research, drug discovery, and public health interventions.