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Lessons learned from the initial sequencing of the pig genome: comparative analysis of an 8 Mb region of pig chromosome 17
Genome Biology
  • Elizabeth A. Hart, Wellcome Trust Sanger Institute
  • Mario Caccamo, Wellcome Trust Sanger Institute
  • Jennifer L. Harrow, Wellcome Trust Sanger Institute
  • Sean J. Humphray, Wellcome Trust Sanger Institute
  • James G. R. Gilbert, Wellcome Trust Sanger Institute
  • Steve Trevanion, Wellcome Trust Sanger Institute
  • Tim Hubbard, Wellcome Trust Sanger Institute
  • Jane Rogers, Wellcome Trust Sanger Institute
  • Max F. Rothschild, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-2007
DOI
10.1186/gb-2007-8-8-r168
Abstract

Background: We describe here the sequencing, annotation and comparative analysis of an 8 Mb region of pig chromosome 17, which provides a useful test region to assess coverage and quality for the pig genome sequencing project. We report our findings comparing the annotation of draft sequence assembled at different depths of coverage. Results: Within this region we annotated 71 loci, of which 53 are orthologous to human known coding genes. When compared to the syntenic regions in human (20q13.13-q13.33) and mouse (chromosome 2, 167.5 Mb-178.3 Mb), this region was found to be highly conserved with respect to gene order. The most notable difference between the three species is the presence of a large expansion of zinc finger coding genes and pseudogenes on mouse chromosome 2 between Edn3 and Phactr3 that is absent from pig and human. All of our annotation has been made publicly available in the Vertebrate Genome Annotation browser, VEGA. We assessed the impact of coverage on sequence assembly across this region and found, as expected, that increased sequence depth resulted in fewer, longer contigs. One-third of our annotated loci could not be fully realigned back to the low coverage version of the sequence, principally because the transcripts are fragmented over several contigs. Conclusion: We have demonstrated the considerable advantages of sequencing at increased read depths and discuss the implications that lower coverage sequence may have on subsequent comparative and functional studies, particularly those involving complex loci such as GNAS.

Comments

This is an article from Genome Biology 8 (2007): 1, doi:10.1186/gb-2007-8-8-r168. Posted with permission.

Rights
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright Owner
Hart et al
Language
en
File Format
application/pdf
Citation Information
Elizabeth A. Hart, Mario Caccamo, Jennifer L. Harrow, Sean J. Humphray, et al.. "Lessons learned from the initial sequencing of the pig genome: comparative analysis of an 8 Mb region of pig chromosome 17" Genome Biology Vol. 8 Iss. 8 (2007) p. 1 - 12
Available at: http://works.bepress.com/max-rothschild/68/