All spin-offs, representing a sample, were created by 303 universities.
"For each point in 3D space, a sample is created in the three signals, which are then manipulated to fit within the audible range of frequency and amplitude".
A reference sample was created by mixing parental mRNA in a 1 to 1 ratio, and was compared to six polyploids (independently resynthesized S0∶1 lines 1200, 5200, and 6400, and their corresponding S5∶6 lines 1250, 5250, and 6450).
A standard sample was created by ligating unmethylated- and methylated-LINE-1 sequences, and cloning into a plasmid (Additional file 2: Figure S2).
A reference sample was created by pooling equal amounts of digested and cleaned DNA from 2 male and 2 female zebra finches.
Plants in each block were sampled at medium stalk position and a pooled sample was created for each block and analyzed by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) for Cd content in leaves.
Using data from NELS:88, a low SES sample was created in which SES was based on family income, family structure and parental education.
A reference blood sample was created by adding 22.9 ± 15.7 MBq (at the time of administration, range: 10.1 to 49.5 MBq of 11C-TMSX in approximately 60 μL to this blood sample and incubated for 10 min at 37°C).
A multi-isolate sample was created using the total RNA samples above and other plant material, collected at the Barah site and a second site.
In parallel, a universal reference RNA sample was created from the spleen of an outgroup of animals (n = 4), which was further amplified to achieve large quantities using Amino Allyl MessageAmp™ II aRNA Amplification (Ambion).
A nationally representative household based sample was created through a stratified, multistage cluster sampling strategy.
