Medical Journals

Ensembl 2006.

Authors:
  • Birney E
  • Andrews D
  • Caccamo M
  • Chen Y
  • Clarke L
  • Coates G
  • Cox T
  • Cunningham F
  • Curwen V
  • Cutts T
  • Down T
  • Durbin R
  • Fernandez-Suarez X M
  • Flicek P
  • Gräf S
  • Hammond M
  • Herrero J
  • Howe K
  • Iyer V
  • Jekosch K
  • Kähäri A
  • Kasprzyk A
  • Keefe D
  • Kokocinski F
  • Kulesha E
  • London D
  • Longden I
  • Melsopp C
  • Meidl P
  • Overduin B
  • Parker A
  • Proctor G
  • Prlic A
  • Rae M
  • Rios D
  • Redmond S
  • Schuster M
  • Sealy I
  • Searle S
  • Severin J
  • Slater G
  • Smedley D
  • Smith J
  • Stabenau A
  • Stalker J
  • Trevanion S
  • Ureta-Vidal A
  • Vogel J
  • White S
  • Woodwark C
  • Hubbard T J P

From: European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK. birney@ebi.ac.uk

Nucleic acids research

  • Publish Date: Jan 2006
  • ISSN: 1362-4962
  • Volume: 34
  • Issue: Database issue
  • Pages: D556-61
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Birney E, Andrews D, Caccamo M, et al. Ensembl 2006.. Nucleic Acids Res. Jan 2006;34:D556-61

Abstract

The Ensembl (http://www.ensembl.org/) project provides a comprehensive and integrated source of annotation of large genome sequences. Over the last year the number of genomes available from the Ensembl site has increased from 4 to 19, with the addition of the mammalian genomes of Rhesus macaque and Opossum, the chordate genome of Ciona intestinalis and the import and integration of the yeast genome. The year has also seen extensive improvements to both data analysis and presentation, with the introduction of a redesigned website, the addition of RNA gene and regulatory annotation and substantial improvements to the integration of human genome variation data.

Mesh Headings (Keywords): Animals, Base Sequence, Databases, Nucleic Acid, Genome, Human, Genomics, Humans, Internet, Mice, Proteins, RNA, Rats, Regulatory Sequences, Nucleic Acid, Sequence Alignment, User-Computer Interface, Variation (Genetics)


Check for Full Text / PubMed Unique Identifier (PMID): 16381931


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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