Genome Browsers



The proliferation of data from genome sequencing over the past decade has brought us into an era where the volume of information available would overwhelm an individual researcher, especially one who is not computationally oriented. The need to make the bare DNA sequence, its properties, and the associated annotations more accessible is the genesis of the class of bioinformatics tools known as genome browsers. Genome browsers provide access to large amounts of sequence data via a graphical user interface. They use a visual, high-level overview of complex data in a form that can be grasped at a glance and provide the means to explore the data in increasing resolution from megabase scales down to the level of individual elements of the DNA sequence. While a user may start browsing for a particular gene, the user interface will display the area of the genome containing the gene, along with a broader context of other information available in the region of the chromosome occupied by the gene. This information is shown in “tracks,” with each track showing either the genomic sequence from a particular species or a particular kind of annotation on the gene. The tracks are aligned so that the information about a particular base in the sequence is lined up and can be viewed easily. In modern browsers, the abundance of contextual information linked to a genomic region not only helps to satisfy the most directed search, but also makes available a depth of content that facilitates integration of knowledge about genes, gene expression, regulatory sequences, sequence conservation between species, and many other classes of data.


Genome Browser European Molecular Biology Laboratory Distribute Annotation System Zoom Level Custom Track 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


  1. Arnaiz O, Cain S, Cohen J, Sperling L (2007) ParameciumDB: a community resource that integrates the Paramecium tetraurelia genome sequence with genetic data. Nucleic Acids Res 35(Database issue):D439–D444CrossRefPubMedGoogle Scholar
  2. Berriman M, Rutherford K (2003) Viewing and annotating sequence data with Artemis. Brief Bioinform 4(2):124–32CrossRefPubMedGoogle Scholar
  3. Brendel V, Kurtz S, Pan X (2007) Visualization of syntenic relationships with SynBrowse. Methods Mol Biol 396:153–63CrossRefPubMedGoogle Scholar
  4. Crabtree J, Angiuoli SV, Wortman JR, White OR (2007) Sybil: methods and software for multiple genome comparison and visualization. Methods Mol Biol 408:93–108CrossRefPubMedGoogle Scholar
  5. Curwen V, Eyras E, Andrews TD, Clarke L, Mongin E, Searle SM et al (2004) The Ensembl automatic gene annotation system. Genome Res 14(5):942–50CrossRefPubMedGoogle Scholar
  6. Dowell RD, Jokerst RM, Day A, Eddy SR, Stein L (2001) The distributed annotation system. BMC Bioinformatics 2:7CrossRefPubMedGoogle Scholar
  7. ENCODE Consortium (2004) The ENCODE (ENCyclopedia Of DNA Elements) Project. Science 306(5696):636–40CrossRefGoogle Scholar
  8. Faga B (2007). Installing and configuring CMap. Curr Protoc Bioinformatics Chapter 9: Unit 9.8Google Scholar
  9. Flicek P, Aken BL, Beal K, Ballester B, Caccamo M, Chen Y et al (2008) Ensembl 2008. Nucleic Acids Res 36(Database issue):D707–D714PubMedGoogle Scholar
  10. Gans JD, Wolinsky M (2007) Genomorama: genome visualization and analysis. BMC Bioinformatics 8:204CrossRefPubMedGoogle Scholar
  11. Hsu F, Kent WJ, Clawson H, Kuhn RM, Diekhans M, Haussler D (2006) The UCSC Known Genes. Bioinformatics 22(9):1036–46CrossRefPubMedGoogle Scholar
  12. Karolchik D, Hinrichs AS, Furey TS, Roskin KM, Sugnet CW, Haussler D et al (2004) The UCSC Table Browser data retrieval tool. Nucleic Acids Res 32(Database issue):D493–6CrossRefPubMedGoogle Scholar
  13. Karolchik D, Kuhn RM, Baertsch R, Barber GP, Clawson H, Diekhans M et al (2008) The UCSC Genome Browser Database: 2008 update. Nucleic Acids Res 36(Database issue):D773–9PubMedGoogle Scholar
  14. Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM et al (2002) The human genome browser at UCSC. Genome Res 12(6):996–1006PubMedGoogle Scholar
  15. Kent WJ, Baertsch R, Hinrichs A, Miller W, Haussler D (2003) Evolution’s cauldron: duplication, deletion, and rearrangement in the mouse and human genomes. Proc Natl Acad Sci USA 100(20):11484–9CrossRefPubMedGoogle Scholar
  16. Lewis SE, Searle SM, Harris N, Gibson M, Lyer V, Richter J et al (2002) Apollo: a sequence annotation editor. Genome Biol 3(12):RESEARCH0082CrossRefPubMedGoogle Scholar
  17. Montgomery SB, Astakhova T, Bilenky M, Birney E, Fu T, Hassel M et al (2004) Sockeye: a 3D environment for comparative genomics. Genome Res 14(5):956–62CrossRefPubMedGoogle Scholar
  18. Pruitt KD, Tatusova T, Maglott DR (2007) NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res 35(Database issue):D61–5CrossRefPubMedGoogle Scholar
  19. Stajich JE, Block D, Boulez K, Brenner SE, Chervitz SA, Dagdigian C et al (2002) The Bioperl toolkit: Perl modules for the life sciences. Genome Res 12(10):1611–8CrossRefPubMedGoogle Scholar
  20. Stein LD, Mungall C, Shu S, Caudy M, Mangone M, Day A et al (2002) The generic genome browser: a building block for a model organism system database. Genome Res 12(10):1599–610CrossRefPubMedGoogle Scholar
  21. Wang H, Su Y, Mackey AJ, Kraemer ET, Kissinger JC (2006) SynView: a GBrowse-compatible approach to visualizing comparative genome data. Bioinformatics 22(18):2308–9CrossRefPubMedGoogle Scholar
  22. Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V et al (2007) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 35(Database issue):D5–12CrossRefPubMedGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  1. 1.Cold Spring Harbor LaboratoryCold Spring HarborUSA

Personalised recommendations