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An obvious reduction in matrix effect was observed by this method compared with microwave assisted extraction followed by purification.
The error due to dissipation factor can be more effectively reduced by this method, compared to the conventional C V measurements.
One specific advantage of the method is that when ensemble mean value is considered as a forecast, the peak flows are predicted with improved accuracy by this method compared to traditional single point forecasted ANNs.
With the higher sensitivity provided by this method compared with immunofluorescence, rare p54nrb/NONO-positive cytoplasmic inclusions were also detected (Fig. 7C and D).
Due to the short reads produced by this method compared to more widely used 454 (Roche) and HiSeq (Illumina) sequencers, the SOLiD platform has not been used before for sequencing of vertebrate sized genomes in a non-model organism.
Consistent with mRNA results, there was an approximately 50%% decrease in TFRC immunofluorescence by this method compared to control cells, exceeding the decrease previously observed in bulk cells (Fig. 4i).
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Although no relation between circulating bone-remodeling markers and sacroiliitis was observed, it is possible that that inflammation of the sacroiliac joints was underestimated by using this method, compared with a more-sensitive method such as magnetic resonance imaging [ 26, 27].
The results obtained by this method compare well with those of the holoTC-RIA (26, 27).
The results obtained by using this method compare well with the reference calculation.
Neutral lipids were extracted from peanut and soybean meals in 50 minutes by this rapid extraction method compared to 1440 minutes required to extract the comparable amount of neutral lipids from a similar sample using the Soxhlet extraction method.
Statistical significant results are indicated by *, method compared with is indicated by number (P < 0.05).
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