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This NimbleGen probe set targets the Vega [ 8], CCDS, and RefSeq gene models, including predicted genes within RefSeq, as well as microRNA (miRNA) [ 9] and regulatory regions for a total target size of 42 Mb.
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Existing uses of models include predicting time and errors for users to perform tasks, acting as embedded assistants to help users perform their tasks, and serving as surrogate users.
Important PM2.5 predictors for the pre-1999 model included predicted PM10 (from Yanosky et al. 2008), extinction coefficient, wind speed, temperature, precipitation, monthly time trend, distance to nearest A1 road, urban land use, block group and county population density, and elevation.
The utilities of such modeling include predicting systems behavior, identifying crucial steps in systems regulation.
Two other studies reported prediction models that include predicted RSA [ 42, 43].
To compensate for sparse monitoring data, the pre-1999 model also included predicted PM10 (PM with aerodynamic diameter < 10 μm) and extinction coefficients (km−1).
Several useful predictions have been obtained from such in-silico models [ 23, 24], including predicting the consequences of gene deletions, optimal growth patterns, outcomes of adaptive evolution and more.
These 17 invalidated models include 11 predicted alleles that were previously considered to be independent genes and six probable pseudogenes that are interrupted by stop codons (Additional file 1).
Annual changes by age group and birth cohort were estimated by applying a linear regression model including the predicted BMI-values (y) based on the models in Table 1 and time (x) for each of the age groups and birth cohorts.
For example, some of the purposes of mathematical computation models include helping predict the likelihood of criminal activity occurring in certain places, creating scenarios in crime analysis and simulating prevention techniques to provide a basis for experimental research that is difficult to produce in real-work settings, and designing critical infrastructure protection [5, 6].
We identified and revised 655 incorrectly predicted gene models, including revisions of intron predictions, intron splice sites and prediction of novel introns.
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