Sentence examples for model organisms typically from inspiring English sources

QTL analysis in humans and model organisms typically detects only a fraction of the predicted number of loci.

Other parturition-related traits, such as placental morphology and source of progesterone, also differ importantly in humans compared to model organisms typically studied and may limit what generalizations can be made [ 3].

Wild-type laboratory strains of model organisms are typically kept in isolation for many years, with the action of genetic drift and selection on mutational variation causing lineages to diverge with time.

To date, microarray techniques have been predominantly used for gene expression analysis particularly for well-studied model organisms for which typically high-quality gene annotation data were available.

Similar problems arise in model organisms; since chemical mutagenesis typically results in many thousands of induced mutations per genome.

Investigators have typically focused on candidate genes selected based on predicted parturition physiology; however, this approach may be limited by the divergence in physiological mechanisms between humans and model organisms that have been typically studied.

Because of the small contribution, through the sperm, of the paternal transcriptome to the fertilized zygote, and because of the stronger maternal contribution to child rearing in most model organisms, parental effects are typically thought of as synonymous with maternal effects, although true paternal effects are known to exist (Rando, 2012).

Not surprisingly, islet architecture and function are dissimilar between humans and typically studied model organisms, such as rodents and zebrafish.

Previous studies in model organisms, including adult mice, have typically shown that 10 20% of eQTL are in trans (e.g. Chow et al. 2015), with the rest acting locally and probably therefore in cis.

Model organisms with short generation times are typically required.

Furthermore, even though DNA microarrays normally use known EST sequences, typically only in model organisms is sufficient sequence information available to examine levels of polymorphism although this is rapidly improving as more sequence information becomes available for non-model organisms.