The first group uses core sample labeled A-1 and oil sample labeled S1 to accomplish the experiment.
For this experiment, oil sample labeled S1 and Core samples labeled A-6, A-7, A-14 and A-15 are selected.
The second group uses oil sample labeled S1 and core samples labeled A-11 and A-16 to accomplish the experiment.
Each of the RNA samples was labeled with red fluorescent dye (Cy5) and hybridized to a DNA microarray together with a reference RNA sample labeled with a green fluorescent dye (Cy3).
By loading an internal common standard sample labeled with a different fluorescent dye, gel-to-gel variations are cancelled out and quantitative proteomic profiling can be achieved across multiple samples [ 11].
For determination of the overall hybridization signals, the sensitivity, and the number of genes detected, a genomic DNA or RNA sample labeled with a single dye was used as previously described [ 28, 29, 53, 54].
Pairwise comparisons were performed on randomly paired individual samples from each group labeled respectively with Cy3 or Cy5 or vice versa and using a mixed sample labeled using Cy2 as an internal standard.
To acquire an image of a sample labeled with paFPs, it is necessary to first grow the cells and express the fusion protein.
Sequencing libraries for C. juglandicola were created by pooling 20 individuals of C. juglandicola collected in Upper Lake, California, United States, into a sample labeled "US", and 20 individuals of C. juglandicola collected in Parnac, France into a sample labeled "France".
The classical strategy of aCGH technique is to co-hybridize genomic DNA from a cancer sample (labelled with one fluorochrome) with genomic DNA from a normal reference sample (labelled with a different fluorochrome) to the aCGH targets.
