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Counting with DNA in metabarcoding studies: how should we convert sequence reads to dietary data?
Bruce E. Deagle, Austen C. Thomas, Julie C. McInnes, Laurence J. Clarket, Eero J. Vesterinen, Elizabeth L. Clare, Tyler R. Kartzinel, J. Paige Eveson
doi: https://doi.org/10.1101/303461
Bruce E. Deagle
*Australian Antarctic Division, Channel Highway, Kingston, Tasmania, Australia
Austen C. Thomas
†Science Department, Smith-Root Inc., Vancouver, Washington, USA
Julie C. McInnes
*Australian Antarctic Division, Channel Highway, Kingston, Tasmania, Australia
Laurence J. Clarket
‡Antarctic Climate & Ecosystems Cooperative Research Centre, University of Tasmania, Tasmania, Australia
*Australian Antarctic Division, Channel Highway, Kingston, Tasmania, Australia
Eero J. Vesterinen
1Biodiversity Unit and Department of Biology, University of Turku, Turku, Finland
¶Department of Agricultural Sciences, University of Helsinki, Helsinki, Finland
Elizabeth L. Clare
2School of Biological and Chemical Sciences, Queen Mary University of London, London, UK
Tyler R. Kartzinel
3Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island, USA
J. Paige Eveson
§CSIRO Oceans and Atmosphere, GPO Box 1538, Hobart, Tasmania, Australia
Posted April 18, 2018.
Counting with DNA in metabarcoding studies: how should we convert sequence reads to dietary data?
Bruce E. Deagle, Austen C. Thomas, Julie C. McInnes, Laurence J. Clarket, Eero J. Vesterinen, Elizabeth L. Clare, Tyler R. Kartzinel, J. Paige Eveson
bioRxiv 303461; doi: https://doi.org/10.1101/303461
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