show Abstracthide Abstract<a href="http://www.thetriaproject.ca/index.php">The Tria Project</a> led by the <a href="http://www.michaelsmith.ubc.ca/faculty/bohlmann">Michael Smith Laboratories at UBC</a> and <a href="http://www.bcgsc.bc.ca/">BCCA Genome Sciences Centre</a> sequenced the ~32.5 Mb genome of <i>Grosmannia clavigera</i> strain kw1407 at ~50X coverage using a hybrid whole genome shotgun (WGS) sequencing method. WGS projects ACXQ00000000 and ACYC00000000 are assembled from the same sequence reads using different methodologies. For ACXQ00000000 (Sanger-454-IlluminaPA) raw Illumina PE reads were assembled using Velvet, and 454 and Sanger reads were assembled with Forge. The two sets of contigs were then combined. For ACYC00000000 (Sanger-454-IlluminaDA) there was no pre-assembly. Filtered genomic DNA reads from Sanger, 454 and Illumina were assembled using the Forge genome assembler.