What can you do with 0.1× genome coverage? A case study based on a genome survey of the scuttle fly <it>Megaselia scalaris </it>(Phoridae)

• Main Authors: Noor Mohamed AF, Rasmussen David A
• Format: Article
• Language: English
• Published: BMC 2009-08-01
• Series: BMC Genomics
• Online Access: http://www.biomedcentral.com/1471-2164/10/382

<p>Abstract</p> <p>Background</p> <p>The declining cost of DNA sequencing is making genome sequencing a feasible option for more organisms, including many of interest to ecologists and evolutionary biologists. While obtaining high-depth, completely assembled genome sequences for most non-model organisms remains challenging, low-coverage genome survey sequences (GSS) can provide a wealth of biologically useful information at low cost. Here, using a random pyrosequencing approach, we sequence the genome of the scuttle fly <it>Megaselia scalaris </it>and evaluate the utility of our low-coverage GSS approach.</p> <p>Results</p> <p>Random pyrosequencing of the <it>M. scalaris </it>genome provided a depth of coverage (0.05x0.1x) much lower than typical GSS studies. We demonstrate that, even with extremely low-coverage sequencing, bioinformatics approaches can yield extensive information about functional and repetitive elements. We also use our GSS data to develop genomic resources such as a nearly complete mitochondrial genome sequence and microsatellite markers for <it>M. scalaris</it>.</p> <p>Conclusion</p> <p>We conclude that low-coverage genome surveys are effective at generating useful information about organisms currently lacking genomic sequence data.</p>