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Related Concept Videos

Genome Annotation and Assembly03:36

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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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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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A Practical Guide to Phylogenetics for Nonexperts
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CIAlign: A highly customisable command line tool to clean, interpret and visualise multiple sequence alignments.

Charlotte Tumescheit1, Andrew E Firth1, Katherine Brown1

  • 1Department of Pathology, University of Cambridge, Cambridge, United Kingdom.

Peerj
|March 21, 2022
PubMed
Summary
This summary is machine-generated.

A new tool, CIAlign, automatically cleans multiple sequence alignments (MSAs) by removing gaps, divergent sequences, and poorly aligned ends. This user-friendly software improves bioinformatics analyses and offers clear visualizations of processed alignments.

Keywords:
Alignment qualityComparative genomicsMultiple sequence alignmentPhylogeneticsPython toolTranscriptomics

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Multiple sequence alignments (MSAs) are fundamental in biological research for analyzing sequence features and relationships.
  • Common issues in MSAs include incomplete sequences, high divergence, large gaps, insertions, deletions, and poorly aligned ends, which can hinder analysis accuracy and speed.
  • Manual MSA editing is prevalent but is labor-intensive and lacks reproducibility.

Purpose of the Study:

  • To develop a user-friendly and comprehensive tool for automated multiple sequence alignment (MSA) trimming.
  • To provide users with customizable options for cleaning MSAs and enhancing the transparency of the process.
  • To offer novel visualization features for improved understanding of alignment processing.

Main Methods:

  • Developed CIAlign, a command-line tool for MSA trimming with multiple customizable options.
  • Implemented functionalities to remove gaps, low-coverage regions (insertions), divergent/short sequences, and poorly aligned ends.
  • Integrated graphical output to visualize alignments before and after processing.

Main Results:

  • CIAlign effectively removes problematic regions and sequences from MSAs.
  • The tool offers customizable parameters for tailored alignment cleaning.
  • Novel visualization options provide clear insights into the trimming process.

Conclusions:

  • CIAlign provides an efficient and transparent solution for automated MSA cleaning.
  • The tool enhances the quality of MSAs for downstream bioinformatics analyses.
  • CIAlign is valuable for researchers needing to refine alignments and visualize large datasets.