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Title: Rapid and accurate sequencing of the rainbow trout physical map using Illumina technology

item MILLER, MICHAEL - University Of Oregon
item Palti, Yniv
item LUO, MING-CHENG - University Of California
item MILLER, JEANNE - University Of Oregon
item BRUNELLI, JOSEPH - Washington State University
item WHEELER, PAUL - Washington State University
item Rexroad, Caird
item THORGAARD, GARY - Washington State University
item DOE, CHRIS - University Of Oregon

Submitted to: Plant and Animal Genome Conference
Publication Type: Abstract Only
Publication Acceptance Date: 11/1/2010
Publication Date: 1/15/2011
Citation: Miller, M.R., Palti, Y., Luo, M., Miller, J.A., Brunelli, J.P., Wheeler, P.A., Rexroad III, C.E., Thorgaard, G.H., Doe, C.Q. 2011. Rapid and accurate sequencing of the rainbow trout physical map using Illumina technology. Plant and Animal Genome Conference. W045.

Interpretive Summary:

Technical Abstract: Rainbow trout (Oncorhynchus mykiss) are the most widely cultivated cold freshwater fish in the world and serve as an important model species for many areas of research. Despite their importance, a reference genome sequence has not yet been generated for rainbow trout due in large part to the complex nature of their genome. A bacterial artificial chromosome (BAC) clone based physical map has been generated that allows genomic complexity to be reduced by analyzing individual BAC clones. To test the feasibility of highly parallel sequencing of rainbow trout BAC clones, we used a combination short fragment paired-end Illumina sequencing of indexed BAC clones and long-fragment mate-pair Illumina sequencing of genomic DNA. Strikingly, we found that this approach can produce high quality assemblies of entire BAC clones with relatively low sequencing coverage, and we are currently using it to sequence 14,766 BAC clones that constitute a minimal tilling path of the rainbow trout physical map. Furthermore, we have created a high-density genetic map with RAD markers that will be useful for ordering the sequence contigs. Our results indicate that this approach will produce a high quality reference genome sequence for rainbow trout and that similar strategies will be useful for sequencing other complex genomes.