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Related Concept Videos

Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Modern Molecular Taxonomy01:29

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Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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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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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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Related Experiment Video

Updated: Nov 16, 2025

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations
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geneRFinder: gene finding in distinct metagenomic data complexities.

Raíssa Silva1,2, Kleber Padovani2, Fabiana Góes3

  • 1Vale Institute of Technology, Boaventura da Silva, 955, Belém, BR, 66055-090, Brazil.

BMC Bioinformatics
|February 26, 2021
PubMed
Summary

geneRFinder is a new machine learning tool that accurately predicts microbial genes in complex metagenomic data. It outperforms existing methods and offers a new benchmark dataset for gene prediction research.

Keywords:
Gene predictionMachine learningMetagenomics

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Metagenomics enables studying microbial communities and their functions through gene analysis.
  • Next-generation sequencing generates large datasets, posing computational challenges for gene prediction.
  • Current gene predictors struggle with metagenomic data complexity and lack standardized benchmarks.

Purpose of the Study:

  • To develop an advanced gene prediction tool for complex metagenomic datasets.
  • To establish a comprehensive benchmark dataset for evaluating gene prediction accuracy in metagenomics.

Main Methods:

  • Developed geneRFinder, a machine learning-based gene predictor utilizing a pre-trained Random Forest model.
  • Created a novel, comprehensive benchmark dataset for gene prediction based on the Critical Assessment of Metagenome Interpretation (CAMI) challenge.

Main Results:

  • geneRFinder demonstrated superior performance compared to state-of-the-art tools like Prodigal and FragGeneScan.
  • Achieved average prediction rate improvements of 54% over Prodigal and 64% over FragGeneScan.
  • Showcased significantly higher specificity rates, outperforming FragGeneScan by 79 percentage points and Prodigal by 66 percentage points.

Conclusions:

  • geneRFinder offers a robust solution for gene prediction across diverse metagenomic complexities.
  • The provided benchmark dataset facilitates standardized evaluation of gene prediction tools.
  • Both geneRFinder and the benchmark dataset are publicly available to advance metagenomic research.