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Related Concept Videos

Polygenic Traits01:18

Polygenic Traits

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When more than one gene is responsible for a given phenotype, the trait is considered polygenic. Human height is a polygenic trait. Studies have uncovered hundreds of loci that influence height, and there are believed to be many more. Due to the high number of genes involved, as well as environmental and nutritional factors, height varies significantly within a given population. The distribution of height forms a bell-shaped curve, with relatively few individuals in the population at the...
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Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

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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...
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Pleiotropy01:33

Pleiotropy

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Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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Human Genetics01:28

Human Genetics

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Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
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Heritability01:06

Heritability

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Heritability is a statistical concept that measures the degree to which genetic differences among individuals contribute to trait variations within a population. It is a fundamental idea in genetics, often prone to misinterpretation. Heritability is expressed as a percentage, reflecting the proportion of variation in a specific trait across a population that can be linked to genetic differences. However, it's important to understand that heritability does not determine how "genetic"...
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Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

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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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Updated: May 24, 2025

Implementation of a Real-Time Psychosis Risk Detection and Alerting System Based on Electronic Health Records using CogStack
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Exploring the application of deep learning methods for polygenic risk score estimation.

Steven Squires1, Michael N Weedon1, Richard A Oram1,2

  • 1Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.

Biomedical Physics & Engineering Express
|February 28, 2025
PubMed
Summary
This summary is machine-generated.

Deep learning (DL) models can accurately generate polygenic risk scores (PRS), even with limited data or missing genetic information. These models show promise in improving PRS generation for clinical and research applications.

Keywords:
deep learninggeneticsmachine learningpolygenic risk scoresprecision medicine

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Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
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Area of Science:

  • Genetics
  • Artificial Intelligence
  • Bioinformatics

Background:

  • Polygenic risk scores (PRS) are crucial for summarizing genetic information.
  • Deep learning (DL) has shown limited impact on PRS generation previously.
  • This study explores DL's potential to enhance PRS creation.

Purpose of the Study:

  • To investigate how deep learning (DL) can improve the generation of polygenic risk scores (PRS).
  • To assess DL model performance in recreating human-programmed PRS and generating multiple PRS from a single model.
  • To evaluate DL's ability to handle missing genetic data and performance constraints.

Main Methods:

  • Training DL models on existing PRS using UK Biobank data.
  • Evaluating DL models for PRS recreation and multi-PRS generation.
  • Assessing DL model performance with reduced training data and missing single nucleotide polymorphisms (SNPs).

Main Results:

  • DL models achieved near-perfect generation of multiple PRS with minimal performance loss, even with reduced training data.
  • For missing SNPs, DL models improved case-population separation (AUC 0.847) compared to traditional PRS (AUC 0.798).
  • DL models demonstrated transferability and longevity.

Conclusions:

  • Deep learning (DL) can accurately generate polygenic risk scores (PRS), including multiple scores from a single model.
  • DL models show promise in improving PRS generation, especially when dealing with missing genetic data.
  • Further advancements may require additional input data.