The 'conditioning on exchangeable parental genotypes' (CEPG) method [ Cordell et al., 2004] is an extension of the CPG approach to detecting parent-of-origin or maternal genotype effects by assuming exchangeability of parental genotypes.
In addition, the generation of isogenic F1 triploids provides a model system for detecting parent-of-origin-specific genome-dosage effects.
By using high performance liquid chromatography it was possible to detect parent drug in the tumours as well as the plasma and tissues after oral administration of TCNU.
In both cases, we were unable to detect parent gene expression in the brain by in situ with probes from brain-derived cDNAs, suggesting that expression levels are either very low and/or brain state-dependent.
In the Netherlands, the law requires preventive child health care (CHC) to detect parenting and developmental problems at an early stage.
The sequencing results for cDNA from reciprocal F1 hybrids were compared to detect parent-of-origin effects.
For example, our method as described has some power to detect parent-child and sibling-sibling relationships (see Additional file 1).
We detected parent-of-origin (PO) biased expression of 48 genes, an equal number of which were expressed with maternal and paternal biases, respectively.
The clinical usefulness of an instrument further depends on its capacity to identify clinical cases, so that it can be used for screening purposes, to detect parents, for whom the bonding process may not adequately develop.
Thus, rather than being unreliable in terms of detecting low parent responsiveness, this rating appears to be less reliable when discriminating between scores at the upper (high responsiveness) end of the scale.
We can express counts as (6) For TDT, we need to construct an index vector for detecting heterozygous parents, i.e. if at least one parent is homozygous and otherwise.
