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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...
Structure of a Gene01:30

Structure of a Gene

A gene is the fundamental unit of heredity. Every individual has two copies of each gene, one inherited from each parent. Although most people contain the same genes, there is a small fraction that is slightly different amongst people. A gene with a small difference in its sequence of DNA bases forms different alleles, contributing to different phenotypes.
However, only 1% of the DNA is composed of genes that encode proteins; the rest, 99% is non-coding DNA. This non-coding DNA performs...
Chromosome Structure02:40

Chromosome Structure

A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
Chromosome Structure02:40

Chromosome Structure

A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
Structural Organization of the Human Body: An Overview01:18

Structural Organization of the Human Body: An Overview

It is convenient to consider the body's structures in terms of fundamental levels of organization that increase in complexity: subatomic particles, atoms, molecules, organelles, cells, tissues, organs, organ systems, and organisms.
To study the chemical level of organization, scientists consider the simplest building blocks of matter: subatomic particles, atoms, and molecules. All matter in the universe is composed of one or more unique pure substances called elements, familiar examples of...

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Related Experiment Video

Updated: Jul 16, 2026

Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.
22:27

Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.

Published on: May 6, 2010

Towards a comprehensive structural coverage of completed genomes: a structural genomics viewpoint.

Russell L Marsden1, Tony A Lewis, Christine A Orengo

  • 1Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT, UK. marsden@biochem.ucl.ac.uk

BMC Bioinformatics
|March 14, 2007
PubMed
Summary

Structural genomics aims to solve protein structures. A combined approach targeting uncharacterized and large protein families is essential for comprehensive structural coverage and evolutionary insights.

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Last Updated: Jul 16, 2026

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Published on: May 6, 2010

Hybrid De Novo Genome Assembly for the Generation of Complete Genomes of Urinary Bacteria using Short- and Long-read Sequencing Technologies
12:08

Hybrid De Novo Genome Assembly for the Generation of Complete Genomes of Urinary Bacteria using Short- and Long-read Sequencing Technologies

Published on: August 20, 2021

Ultra-long Read Sequencing for Whole Genomic DNA Analysis
10:34

Ultra-long Read Sequencing for Whole Genomic DNA Analysis

Published on: March 15, 2019

Area of Science:

  • Structural biology
  • Genomics
  • Protein science

Background:

  • Structural genomics initiatives aim for large-scale protein structure determination.
  • The Protein Structure Initiative (PSI) focuses on structurally uncharacterized protein families.
  • Understanding the distribution of these families is crucial for comprehensive structural coverage.

Purpose of the Study:

  • To assess the number and distribution of protein families lacking structural representation.
  • To determine the accessibility of uncharacterized families to high-throughput structural genomics pipelines.
  • To evaluate strategies for achieving comprehensive structural coverage of protein families.

Main Methods:

  • Comprehensive domain annotation of genomes using CATH, Pfam-A, and Newfam domain families.
  • Analysis of structurally uncharacterized families accessible to high-throughput pipelines.
  • Measurement of domain coverage across genomes.

Main Results:

  • Derived comprehensive domain annotation of genomes.
  • Identified proportions of uncharacterized families accessible to high-throughput pipelines, particularly those with prokaryotic orthologues.
  • Demonstrated benefits of selecting targets from both uncharacterized and large characterized protein superfamilies for domain coverage.

Conclusions:

  • A combined target selection strategy is essential for structural genomics.
  • This approach is key to achieving comprehensive structural coverage of genomes.
  • Leads to greater insights into protein structure and evolutionary mechanisms.