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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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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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Comparing Copy Number Variations and SNPs02:26

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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%...
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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
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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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Using Local Convolutional Neural Networks for Genomic Prediction.

Torsten Pook1, Jan Freudenthal2, Arthur Korte2

  • 1Animal Breeding and Genetics Group, Department of Animal Sciences, Center for Integrated Breeding Research, University of Goettingen, Göttingen, Germany.

Frontiers in Genetics
|December 7, 2020
PubMed
Summary
This summary is machine-generated.

Local convolutional neural networks (LCNN) show promise for genomic prediction, outperforming traditional artificial neural networks (ANNs) in livestock and crop breeding. While effective for large datasets, LCNNs may not be superior to established methods in small populations.

Keywords:
Kerasbreedingdeep learninggenomic selectionmachine learningphenotype predictionselection

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Area of Science:

  • Genetics and breeding
  • Bioinformatics
  • Machine learning in agriculture

Background:

  • Genomic prediction is crucial for livestock and crop breeding, aiming to predict breeding values and phenotypes.
  • Artificial neural networks (ANNs) offer potential for genomic prediction, with local convolutional neural networks (LCNNs) showing promise due to their region-specific filtering capabilities.

Purpose of the Study:

  • To evaluate the performance of LCNNs for genomic prediction compared to traditional ANNs and state-of-the-art methods.
  • To assess the impact of LCNN architecture on predictive ability across different datasets and trait heritabilities.

Main Methods:

  • Utilized simulated maize and real Arabidopsis datasets for performance evaluation.
  • Compared LCNNs against multi-layer perceptrons, convolutional neural networks, genomic best linear unbiased prediction (GBLUP), and Bayesian models.
  • Investigated the effect of LCNN kernel size, stride, and fully connected layer configurations.

Main Results:

  • Baseline LCNN outperformed other ANNs for most traits across both datasets.
  • LCNNs showed superior predictive ability (up to 24% increase) over GBLUP and Bayesian models for high heritability traits in large populations.
  • State-of-the-art methods outperformed ANNs in small training populations, though LCNNs still showed a ~10% advantage over other ANNs.

Conclusions:

  • LCNNs represent a promising advancement in genomic prediction, particularly for large-scale datasets and complex genetic architectures.
  • While ANNs offer flexibility for incorporating diverse data inputs, challenges remain regarding heritability estimation and the additive nature of breeding values.
  • Continued advancements in phenotyping and genotyping may position ANNs as a viable alternative for genomic prediction in breeding programs.