Sentence examples for marker contribution from inspiring English sources

Relaxing the GBLUP assumption of equal marker contribution by increasing the weight that is given to a specific marker in the construction of the trait-specific G resulted in increased predictive performance.

When information on marker contribution was provided from different sources (SM, RR, BL), it was possible to weight the contribution to the genomic matrix by the marker-specific realized variance.

Our study aimed at testing different sources of information in order to weight marker contributions into the genomic relationship matrix and relax the assumption of equal contributions from all markers to additive genetic variability among individuals.

They could also serve as background in the search for different sources of information to weight marker contributions in the genomic matrix, and markers could be weighted relying on functional information about the annotated genes that lie in their proximity.

With real data, de los Campos et al. [ 7] found that weighting marker contributions in the construction of G improved prediction for height in humans, which is a trait with high heritability and a large number of QTL [ 33].

While evaluation of a candidate marker's contribution to a panel in specimens from women with clinically apparent ovarian cancer may be a poor predictor of its lead time and utility in early detection, it provides a useful filter for gaining access to precious pre-clinical specimens.

The probability of observing a marker includes contributions from living cells with periodically present markers and dead cells with constantly present markers.

The quality of derived ESCs was assessed on the basis of three criteria: expression of stem cell markers, chimeric contribution and germline transmission.

The mean chi squared contributions, the markers average contribution to the goodness-of-fit, were less than 2. Primers were designed to produce a 276 bp mixed amplicon of the three BnaFAD2 copies present within B. napus cultivar Cabriolet and a 176 bp amplicon specific for BnaC.GL2.b. (see Additional file 9) The forward primer of each amplicon had a 5' M13(−21) tail (Additional file 5: Table S5).

The broad range of PR expression in clinical specimens suggests that PR-dependent gene expression may provide a more accurate marker of PR contribution to breast cancer phenotypes.

As a broad range of PR protein expression is observed clinically, a PR gene signature would provide a valuable marker of PR contribution to early breast cancer progression.