These vast data were used to identify SSR motifs specific for the tested chromosome arms or whole chromosomes and we tested this information by their physical localization on metaphase chromosomes.
The study does not test whether this information was useful enough to allow investors to make sufficient profit trading on it to justify the extra risk.
If there is sufficient evidence (defined with the same quality metrics as above) to determine that the given individual does not have an alternative allele at the tested location, this information is stored in the database as a "SARA" (Same As Reference Assembly) position, which can be thought of as a computational genotyping assay.
The results of these experimental tests are discussed in the paper with emphasis on the correlation between the roughness of the surface and the outcomes of both shear and pull-out tests; this information can be used in design in order to prescribe the minimum roughness level necessary to attain the expected debonding strength of the reinforcement.
In regular ELISA group, the strain used to extract antigens for the test was not specified in 68 (58.2%), and in all the commercial tests this information was not available; in 59 (50.7%) tests the T. cruzi life cycle form used as sources of antigens was not specified, and in 65 (56.0%) antigen purification was not specified or not clear in the report.
To test this, we gathered information about the age and the number of children parents had.
To test this hypothesis valid information using lateral cephalographs for the analysis of sagittal jaw position and the neutral vertebrae in the radiological Cobb-angle definition might have been used.
To test this further, additional information has to be measured on an individual level, which we prompt future studies to take into account if not using the exact method.
To test this, we used information on the region of ascertainment that was available from the UK 1958 Birth Cohort and UK Blood Service, and analysed genotype frequencies based on subdivisions of the UK into four major regions, namely (1) Scotland, (2) northern England, (3) Midlands and (4) southern England (see ESM Fig. 2).
We were able to investigate the association between air pollutant concentrations and preterm births for a large number of births in metropolitan Sydney between 1998 and 2000 and we were able to test this association using information on infants born to women residing within 5 kilometres of an air monitoring station, again for a large number of births.
