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Related Concept Videos

Genome Annotation and Assembly03:36

Genome Annotation and Assembly

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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.
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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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Genomic Imprinting and Inheritance02:30

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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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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 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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Genomic DNA in Prokaryotes00:46

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The genome of most prokaryotic organisms consists of double-stranded DNA organized into one circular chromosome in a region of cytoplasm called the nucleoid. The chromosome is tightly wound, or supercoiled, for efficient storage. Prokaryotes also contain other circular pieces of DNA called plasmids. These plasmids are smaller than the chromosome and often carry genes that confer adaptive functions, such as antibiotic resistance.
Genomic Diversity in Bacteria
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Whole-Genome Annotation with BRAKER.

Katharina J Hoff1, Alexandre Lomsadze2, Mark Borodovsky3,4,5

  • 1University of Greifswald, Institute of Mathematics and Computer Science, Greifswald, Germany. katharina.hoff@uni-greifswald.de.

Methods in Molecular Biology (Clifton, N.J.)
|April 26, 2019
PubMed
Summary

BRAKER is a fully automated pipeline for accurate gene prediction in eukaryotic genomes. It integrates multiple evidence types to enhance gene finding accuracy, making it a versatile tool for genomic research.

Keywords:
AUGUSTUSBRAKERGene predictionGeneMark-ES/ETGenome annotation pipelineProtein mapping to genomeProtein-coding genesRNA-Seq reads

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Accurate gene prediction is crucial for understanding eukaryotic genome function.
  • Existing gene prediction tools often require manual parameterization or lack flexibility in integrating diverse evidence types.

Purpose of the Study:

  • To present BRAKER, a highly accurate and fully automated pipeline for eukaryotic gene prediction.
  • To describe the methodology and application of BRAKER with various combinations of extrinsic evidence.

Main Methods:

  • BRAKER combines GeneMark-ES/ET for automated parameter learning and AUGUSTUS for accurate gene finding.
  • It integrates extrinsic evidence, including RNA-Seq read footprints, cross-species protein alignments, and heterogeneous data.
  • The pipeline refines models using available evidence during both training and prediction steps.

Main Results:

  • BRAKER achieves highly accurate and fully automated gene prediction in novel eukaryotic genomes.
  • The pipeline demonstrates flexibility in utilizing diverse extrinsic evidence, enhancing prediction robustness.
  • Previous versions like BRAKER1 established foundational integration of RNA-Seq data.

Conclusions:

  • BRAKER provides a robust and automated solution for gene prediction in eukaryotic genomes.
  • Its ability to integrate heterogeneous evidence makes it adaptable to various genomic research scenarios.
  • The pipeline facilitates efficient and accurate analysis of novel eukaryotic genomes.