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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.
Genomics02:02

Genomics

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...
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...
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
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Modern Molecular Taxonomy01:29

Modern Molecular Taxonomy

Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
Conservation of Protein Domains Over Different Proteins02:26

Conservation of Protein Domains Over Different Proteins

Protein domains are small structurally independent units that are part of a single amino acid chain.  Although these domains are often structurally independent, they may rely on synergistic effects to perform their functions as part of a larger protein. Protein domains may be conserved within the same organism, as well as across different organisms.
A limited set of protein domains often duplicate and recombine during evolution. These domains can be organized in different combinations to form...

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Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms
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Current challenges in genome annotation through structural biology and bioinformatics.

Nicholas Furnham1, Tjaart A P de Beer, Janet M Thornton

  • 1EMBL-EBI, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, UK.

Current Opinion in Structural Biology
|August 14, 2012
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Summary

Accurate gene product annotation is crucial for understanding genomic data. Experimentally determined structures aid computational biologists in identifying homology and improving functional annotations for enzymes.

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Area of Science:

  • Genomics
  • Structural Biology
  • Bioinformatics

Background:

  • High-throughput sequencing projects generate vast amounts of genomic data.
  • Accurate gene product annotation is essential but challenging for computational biologists.
  • Experimental data, particularly 3D structures, is vital for annotating unknown gene functions.

Purpose of the Study:

  • To highlight the importance of experimentally determined structures in genomic annotation.
  • To emphasize the role of structural information in detecting sequence-based homology.
  • To showcase how structural data aids in understanding molecular-level consequences of genomic variation.

Main Methods:

  • Utilizing experimentally determined protein structures.
  • Integrating structural data with sequence and chemical similarity.
  • Applying bioinformatics methods for functional annotation.

Main Results:

  • Experimentally determined structures enable detection of homology missed by sequence analysis alone.
  • Structural information allows for the molecular-level interpretation of genomic variations.
  • Combining structural, sequence, and chemical data enhances enzyme functional annotation.

Conclusions:

  • Experimentally determined structures are indispensable for accurate and detailed genomic annotation.
  • Structural biology plays a critical role in advancing computational biology and functional genomics.
  • Integrating diverse data types, including structure, sequence, and chemistry, is key to robust functional annotation.