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Article title
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Abstract
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Keywords
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Introduction
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Studies to date
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Early DNA studies using whole specimens
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Early eDNA-like studies
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Conventional PCR
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Nanoparticle technologies: Carbon nanotube and light transmission spectroscopy
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Quantitative PCR
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Droplet Digital PCR
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High-throughput sequencing
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Loop-mediated isothermal amplification
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Target type
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Summary, including paths forward and critical remaining gaps
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Assay/Metabarcode choice
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Sampling effort
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Field portable instruments (and PCR inhibition)
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Quantification accuracy
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Degradation in natural settings
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Translating eDNA survey results into AIS management action
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Conclusions
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Acknowledgements
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References
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