Data from: Extracellular DNA extraction is a fast, cheap and reliable alternative for multi-taxa surveys based on soil DNA
Data files
Jan 20, 2017 version files 18.07 MB
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Nouragues2013_Plants_GH_uniq.fasta
31.93 KB
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README_for_Nouragues2013_Plants_GH_uniq.txt
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README_for_Zinger_et_al_SBB_extracellular_filtered.tar.txt
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README_for_Zinger_et_al_SBB_extracellular_rawdata_uniq.tar.txt
2.78 KB
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Zinger_et_al_SBB_extracellular_filtered.tar.gz
1.37 MB
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Zinger_et_al_SBB_extracellular_rawdata_uniq.tar.gz
16.65 MB
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Zinger_et_al_SBB_extracellular_samples.txt
8 KB
Abstract
DNA metabarcoding on soil samples is increasingly used for large-scale and multi-taxa biodiversity studies. However, DNA extraction may be a major bottleneck for such wide uses. It should be cost/time effective and allow dealing with large sample volumes so as to maximise the representativeness of both micro- and macro-organisms diversity. Here, we compared the performances of a fast and cheap extracellular DNA extraction protocol with a total DNA extraction method in retrieving bacterial, eukaryotic and plant diversity from tropical soil samples of ca. 10 g. The total DNA extraction protocol yielded more high-quality DNA. Yet, the extracellular DNA protocol provided similar diversity assessments although it presented some differences in clades relative abundance and undersampling biases. We argue that extracellular DNA is a good compromise between cost, labor, and accuracy for high-throughput DNA metabarcoding studies of soil biodiversity.