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Both were processed with the MDSInit approach using adjusted weighting.
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The groups from both experiments were processed with the same pipeline for positive selection, with the exception of alignment trimming using trimAl (version 1.2rev59), only executed in FILTER experiment.
Samples from both mice and monkeys were processed with the following ELISA protocol.
Both linking and cutting structures were processed with 100% yield.
Binding data were processed with both MAT (Model-based Analysis of Tiling-arrays) [67] and TAS (Tiling Analysis Software, from Affymetrix).
All eight scans were processed with both procedures, and ICCs were measured for cerebral (gray and white matter) volumes.
All samples were processed with both anti-albumin and anti-betalactoglobulin tips using a Versette Automated Liquid Handler (Thermo Fisher Scientific) as previously described [ 25].
For both TESS and STRUCTURE analyses, outputs were processed with CLUMPP v1.1.2 (Jakobsson and Rosenberg 2007), to identify distinct clustering solutions in the replicated runs for each K value.
For both ECM1 and D2-40 slidesng, slides were processed with antigen retrieval which was achieved by boiling the slides in citrate buffer (pH 6.0) for 1.5 min. For VEGF-C staining, slides were boiled in an EDTA solution for 20 min before cooling.
Data were processed with AMIDE [21].
Images were processed with ImageJ and Photoshop.
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