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Related Concept Videos

Phylogenetic Trees03:21

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Genomics02:02

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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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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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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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Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
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Related Experiment Video

Updated: Feb 10, 2026

A Practical Guide to Phylogenetics for Nonexperts
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Evaluation of phylogenetic reconstruction methods using bacterial whole genomes: a simulation based study.

John A Lees1,2, Michelle Kendall3, Julian Parkhill1

  • 1Infection Genomics, Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SA, UK.

Wellcome Open Research
|May 19, 2018
PubMed
Summary

Comparing phylogenetic reconstruction methods for bacterial genomes reveals that while maximum likelihood is most accurate, faster genetic distance methods offer comparable results. Gene choice significantly impacts tree accuracy, with conserved genes affecting topology and recombination genes affecting branch lengths.

Keywords:
bacteriaphylogenetic methodsphylogenysimulationtree distance

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Area of Science:

  • Computational Biology
  • Evolutionary Biology
  • Genomics

Background:

  • Phylogenetic reconstruction is crucial for bacterial population genomics.
  • Numerous phylogenetic inference methods exist with varying strengths and weaknesses.
  • Unbiased comparisons of these methods are scarce.

Purpose of the Study:

  • To compare the accuracy and computational efficiency of diverse phylogenetic reconstruction methods.
  • To evaluate the impact of different gene sets on phylogenetic inference.
  • To provide guidance on selecting appropriate phylogenetic methods based on accuracy and speed.

Main Methods:

  • Simulated whole genome data from a known phylogenetic tree using a realistic evolutionary model.
  • Inferred phylogenies using a range of methods, including maximum likelihood and genetic distance-based approaches.
  • Validated methods using real bacterial genome alignments (Streptococcus pneumoniae) and compared core gene trees to a core genome tree.

Main Results:

  • Maximum likelihood methods yield the most accurate phylogenies but are computationally intensive.
  • Faster genetic distance methods provide comparable accuracy, suitable for rapid phylogenetic inference.
  • Highly conserved genes (e.g., translation-related) can lead to inaccurate tree topology, while recombination-associated genes can distort branch lengths.

Conclusions:

  • Recommended phylogenetic reconstruction approaches balance accuracy and computational demands.
  • Faster methods are viable for many analyses, with high-quality alignment being a key factor for accurate topology.
  • Released simulated data and code to facilitate future method comparisons.