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After digestion, the samples were filtered through Cell Strainer (BIOFIL).
Samples were filtered for regions blacklisted by the ENCODE project.
Samples were filtered through 0.45 μm membranes prior to quatification of glucose, xylose and xylitol.
Suspected germline variants based on the allele frequency of normal samples were filtered out.
Culture samples were filtered onto preweighed filters (Sartorius membrane filter 0.45µm).
After 30-min incubation, the samples were filtered through a nitrocellulose membrane and washed with a reaction buffer.
Sonicated samples were filtered through a 5 µm nylon membrane to remove possible minerals and coarse materials.
Before analysis, the samples were filtered through 0.22 μm syringe filter, which was then injected for the analysis.
Samples were filtered through 0.22 μm membrane filters (Millipore) and centrifuged at 13,000 g for 10 min.
At the end of this incubation experiment, DOC samples were filtered through combusted Whatman GF/F filters to remove bacteria.
After 30 min incubation, the samples were filtered through a nitrocellulose membrane and washed with reaction buffer.
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