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Updated: Jun 20, 2026

Hybrid De Novo Genome Assembly for the Generation of Complete Genomes of Urinary Bacteria using Short- and Long-read Sequencing Technologies
Published on: August 20, 2021
De novo genome sequence assembly of a filamentous fungus using Sanger, 454 and Illumina sequence data
Scott Diguistini1, Nancy Y Liao, Darren Platt
1Department of Wood Science, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada. scottdig@interchange.ubc.ca
Abstract:
Sequencing-by-synthesis technologies can reduce the cost of generating de novo genome assemblies. We report a method for assembling draft genome sequences of eukaryotic organisms that integrates sequence information from different sources, and demonstrate its effectiveness by assembling an approximately 32.5 Mb draft genome sequence for the forest pathogen Grosmannia clavigera, an ascomycete fungus. We also developed a method for assessing draft assemblies using Illumina paired end read data and demonstrate how we are using it to guide future sequence finishing. Our results demonstrate that eukaryotic genome sequences can be accurately assembled by combining Illumina, 454 and Sanger sequence data.
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