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The ability to generate very deep sequence analysis of a DNA sample in a very short time allows the investigation of many complex samples with meta-genomic analysis.
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These limitations hinder the use of MRE for detection in many real world complex samples, such as biological fluids and food matrices.
However, discovering multiple protein biomarkers by measuring many proteins simultaneously (proteomics) in complex samples like blood has proven difficult for reasons of coverage, precision, throughput, preanalytical variability, and cost [20].
Additionally, MS can be coupled to chromatographic techniques; these previous separation processes can be widely modified and/or enhanced in order to assist the analyst to have great control among the many different species present in any complex samples, such as biological fluids (Bonnefont-Rousselot and Collin 2010).
In order to be used to analyze complex samples like blood, which contain many different molecules, the nanotube sensors will be organized into arrays.
When analysing complex samples such as food supplements, many other matrix components are unavoidably co-extracted together with the target analytes.
Thus, it is necessary to collect samples from proximal sites that include many complex ash particles if a statistically significant population of the larger bubbles are sought.
In many instances counting by microscopy may become prohibitively expensive, particularly for complex samples with low contrast and varied particle shapes.
As with many complex diseases, identifying susceptibility genes for haloperidol-induced ADR in humans will require sample sizes that are very large (>5000).
The Th4+ ion forms many complex ions.
There were many complex challenges.
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CEO of Professional Science Editing for Scientists @ prosciediting.com