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Related Concept Videos

Genomics02:02

Genomics

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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Genetic Variation01:25

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Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
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Genetic Screens02:46

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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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Combinatorial Gene Control02:33

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Combinatorial gene control is the synergistic action of several transcriptional factors to regulate the expression of a single gene. The absence of one or more of these factors may lead to a significant difference in the level of gene expression or repression.
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Genome-wide Association Studies-GWAS01:11

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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.
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Human Genetics01:28

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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.
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Related Experiment Video

Updated: Feb 26, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
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GenoCore: A simple and fast algorithm for core subset selection from large genotype datasets.

Seongmun Jeong1, Jae-Yoon Kim1,2, Soon-Chun Jeong3

  • 1Personalized Genomic Medicine Research Center, Division of Strategic Research Groups, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea.

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|July 21, 2017
PubMed
Summary
This summary is machine-generated.

GenoCore software efficiently identifies core subsets from large plant genotype datasets. This tool aids in genome-wide association studies and crop breeding by ensuring accurate and representative sample selection.

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Area of Science:

  • Plant genetics
  • Bioinformatics
  • Computational biology

Background:

  • Selecting core subsets from plant genotype data is crucial for cost-effective and timely analyses in genome-wide association studies (GWAS) and crop breeding.
  • The increasing volume of genetic markers from high-density SNP arrays and NGS data necessitates efficient software for core subset extraction.

Purpose of the Study:

  • To develop a novel program, GenoCore, for the rapid and efficient identification of genetically coherent and representative core subsets from large plant genotype datasets.
  • To introduce simple coverage and diversity scores for accurate sample selection reflecting genotype errors and genetic variation.

Main Methods:

  • GenoCore utilizes simple measures of coverage and diversity scores to assess genotype errors and genetic variation.
  • The program was compared against existing core collection software using various datasets, evaluating genetic distance, diversity, coverage, system resource usage, and sample size.

Main Results:

  • GenoCore efficiently identifies the smallest, most consistent, and representative core collection.
  • The software demonstrates greater genetic coverage compared to other tested methods.
  • GenoCore operates with less memory and more efficient scoring.

Conclusions:

  • GenoCore provides an efficient solution for selecting core subsets from large plant genotype datasets.
  • The software aids in accelerating genomic analyses and improving crop breeding strategies.
  • GenoCore is implemented in R and publicly accessible for use.