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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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LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
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Transposons01:24

Transposons

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Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...
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Genomic DNA in Eukaryotes

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Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
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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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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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Updated: May 1, 2026

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
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TraV: a genome context sensitive transcriptome browser.

Sascha Dietrich1, Sandra Wiegand1, Heiko Liesegang1

  • 1Abteilung für Angewandte und Genomische Mikrobiologie, Institut für Mikrobiologie und Genetik, Norddeutsches Zentrum für Mikrobielle Genomforschung, Georg-August-Universität Göttingen, Göttingen, Germany.

Plos One
|April 9, 2014
PubMed
Summary
This summary is machine-generated.

TraV is a new RNA-Seq analysis tool designed to handle multiple transcriptome sequencing experiments efficiently. It visualizes nucleotide activities for prokaryotic RNA-seq data, overcoming memory and processing limitations of current tools.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Next-generation sequencing (NGS) technologies generate vast amounts of genomic data, particularly for transcriptional analysis.
  • Existing RNA-Seq analysis and visualization tools struggle with large datasets, often limited to processing only two to three samples simultaneously due to memory and processing constraints.

Purpose of the Study:

  • To develop an efficient RNA-Seq analysis and visualization tool capable of processing multiple transcriptome sequencing experiments.
  • To address the limitations of current tools in handling large-scale prokaryotic RNA-seq data.

Main Methods:

  • Development of TraV, a novel RNA-Seq analysis and visualization tool.
  • Implementation of analytical methods specifically for prokaryotic RNA-seq experiments.
  • Calculation of single nucleotide activities from mapping information for memory-efficient analysis.

Main Results:

  • TraV successfully processed fifteen transcriptome sequencing experiments of Bacillus licheniformis DSM13.
  • The tool utilizes nucleotide activities, significantly improving memory efficiency and reducing processing overhead compared to single read mapping.
  • TraV enables the visualization and analysis of multiple transcriptome sequencing experiments simultaneously.

Conclusions:

  • TraV offers a memory-efficient and effective solution for analyzing and visualizing multiple prokaryotic RNA-seq experiments.
  • The nucleotide activity approach overcomes the limitations of existing tools, facilitating deeper insights into transcriptional activities from large datasets.