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Shared OTUs (at genus level) between different samples was viewed using online tool Venny (http://www.bioinfogp.cnb.csic.es/tools/venny/index.html).html
The scintillation light from the crystal was viewed using a single 1×1 cm2 silicon PIN diode.
The resulting digestion products were resolved by agarose gel electrophoresis using 1.5% agarose (w/v) gel running for 90 min at 70 V and the gel was viewed using Alpha Imager HP Gel-documentation system (Cell bioscience, USA).
Sequence alignments were performed using the Clustal_W program [17] and the calculated phylogenetic tree was viewed using Mega4.0 Beta program [27].
NBD fluorescence was viewed using a Plan-APO 100×/1.3 NA oil objective with the following filter set: BP 450 490, FT 510, and BP 512 542.
Amino acid sequence alignments were performed using the Clustal_W program [22] and the calculated phylogenetic tree was viewed using Mega 3.1 Beta program [23].
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The remaining 5% was viewing using physical media such as DVDs.
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Slides were viewed using a Leica LEITZ DMRX epifluorecence microscope.
Likewise, discipline and subfield results can be viewed using the same criteria.
These minimalist 3D artworks can then be viewed using anaglyphic glasses.
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