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Related Concept Videos

Genomics02:02

Genomics

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...
Improving Translational Accuracy02:07

Improving Translational Accuracy

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...
Gene Duplication and Divergence02:37

Gene Duplication and Divergence

The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Improving Translational Accuracy02:07

Improving Translational Accuracy

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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Accurate <i>ab initio</i> gene prediction in eukaryotes with Tiberius in multiple clades.

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Related Experiment Video

Updated: Jun 12, 2026

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens
09:14

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Published on: June 28, 2018

Tiberius: end-to-end deep learning with an HMM for gene prediction.

Lars Gabriel1,2, Felix Becker1,2, Katharina J Hoff1,2

  • 1Institute of Mathematics and Computer Science, University of Greifswald, Greifswald 17489, Germany.

Bioinformatics (Oxford, England)
|November 19, 2024
PubMed
Summary

Tiberius, a novel deep learning gene predictor, significantly improves ab initio eukaryotic gene prediction accuracy. This method integrates advanced layers and a differentiable HMM, outperforming existing tools and achieving high accuracy in mammalian genomes.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Eukaryotic gene prediction has historically relied on Hidden Markov Models (HMMs) for over 25 years.
  • Recent advancements show deep learning combined with HMMs can enhance ab initio gene prediction accuracy.

Purpose of the Study:

  • To introduce Tiberius, a novel deep learning-based ab initio gene predictor.
  • To improve the accuracy and efficiency of eukaryotic gene prediction.

Main Methods:

  • Tiberius integrates convolutional and long short-term memory layers with a differentiable HMM layer.
  • A custom gene prediction loss function was utilized.
  • The model was trained on mammalian genomes and evaluated on human and other genomes.

Main Results:

  • Tiberius significantly outperforms existing ab initio methods, achieving a 62% F1 score on the human genome.
  • It accurately predicts the exon-intron structure of human genes in de novo mode.
  • Tiberius's accuracy rivals methods using external data, and it is the fastest state-of-the-art gene prediction tool.

Conclusions:

  • Tiberius represents a significant advancement in ab initio eukaryotic gene prediction.
  • Its deep learning architecture and integrated HMM offer superior accuracy and speed.
  • This tool has the potential to accelerate genomic research by improving gene structure identification.