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Related Concept Videos

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.
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Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes

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...
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

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...
RNA-seq03:21

RNA-seq

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. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...

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Related Experiment Video

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Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples
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Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples

Published on: December 22, 2014

Reference-independent comparative metagenomics using cross-assembly: crAss.

Bas E Dutilh1, Robert Schmieder, Jim Nulton

  • 1Centre for Molecular and Biomolecular Informatics, Nijmegen Centre for Molecular Life Sciences, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands. dutilh@cmbi.ru.nl

Bioinformatics (Oxford, England)
|October 18, 2012
PubMed
Summary
This summary is machine-generated.

This study introduces crAss, a bioinformatic tool for analyzing cross-assembly files. It reveals similarities between metagenomic samples, improving comparative metagenomics by utilizing unknown sequences.

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Area of Science:

  • Bioinformatics
  • Metagenomics
  • Computational Biology

Background:

  • Metagenomes contain many unknown sequences, often ignored in analyses, leading to biased conclusions.
  • Comparative metagenomics studies relationships between different metagenomic samples.
  • Cross-assembly links homologous reads from multiple samples without reference databases.

Purpose of the Study:

  • To introduce a novel bioinformatic tool for analyzing cross-assembly data.
  • To enable efficient comparative metagenomics by incorporating previously unanalyzed sequences.
  • To provide insights into metagenomic sample similarities.

Main Methods:

  • Development of the crAss bioinformatic tool.
  • Utilizing cross-assembly of reads from multiple metagenomic samples.
  • Analysis of cross-assembly files to determine sample relationships.

Main Results:

  • The crAss tool facilitates fast and simple analysis of cross-assembly files.
  • It generates distances between all pairs of metagenomic samples.
  • An insightful visualization displays the similarities between samples.

Conclusions:

  • crAss enhances comparative metagenomics by enabling the analysis of previously ignored unknown sequences.
  • The tool provides a fast and intuitive method for assessing metagenomic sample relationships.
  • Cross-assembly analysis with crAss offers a more comprehensive understanding of metagenomic data.