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As such, we recommend that genes with a normalized count value less than this data-driven threshold in all samples be filtered from subsequent differential analyses.
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Reads not passing quality criteria (uniquely classified IGHV, IGHJ, and H-CDR3) were filtered from subsequent analysis.
Ectopic beats were filtered from raw recordings.
All probe sets with absent calls for every mixture were filtered out from subsequent analyses as corresponding to non-expressed transcripts.
To eliminate computationally non-informative and background probe sets, probe sets with CV values < 5% or average expression levels < 6 (in the log-2 scale) across samples were filtered out from subsequent analysis.
From there, they would be filtered, with "threatening" protesters detained.
The adaptor sequences were filtered out from the subsequent analysis and the resulting reads were aligned using Bismark software [ 37].
We identified five factors that possibly play a role when abstracts are filtered on their way from meeting submission to subsequent publication.
Aliquots of 0.5 ml from different pigment solutions were filtered through syringe filters with 0.2 µm of pore diameter for subsequent injection in an HPLC system.
Once metagenomic sequences were annotated, KO information was filtered and extracted in the annotation profile from MG-RAST for subsequent metabolic network reconstruction.
For soluble chemical analysis, each sample was filtered through 0.2 µm syringe filters and stored at −20 °C for subsequent analysis.
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