Sentence examples for missing data option from inspiring English sources

I used case weights and the missing data option in Mplus in order to account for stratification, cluster effects, and cases with incomplete data.

The missing data option in Mplus was implemented to avoid list-wise deletion.

An additional 119 individuals who had a minimum of four genotypes of the six SNPs in stage 2 were included in this analysis (n = 2676) using a missing data option that substituted the population mean genotypic value for missing SNPs.

Although multiple imputation of missing data is an option, it requires a number of assumptions.

NSSI = non-suicidal self-injury, n = 808 in the model of social functions, due to listwise deletion of missing data being default option in the heteroscedasticity-consistent standard error (HCSE) macro [ 53], † including alcohol abuse, mental health problems, in jail, handicap, separated from parent(s), divorce, quarreling during divorce, ** p <.01, *** p <.001.

To handle gaps and missing data, the pairwise-deletion option was selected.

Treating gaps as unknown or missing data is the default option in PAUP* The FAQ page for PAUP* at explains the working of this treatment under each inference method, and for PhyML and Bayesian, it is explained in [ 27- 29].

To minimise missing data, the "auto-fill" option on the Actiheart software, which fills gaps of up to two hours with the average values calculated from the recorded portion of the same day, was used.

The procedure employed here for dealing with missing data caused by N/A options was used by Bradley et al [ 17] in order to retain sufficient data to carry out the psychometric analyses and to make best use of the available data.

All character state changes were given equal weight, all characters were unordered, gaps were treated as missing data, and the amb- option was used so that internal branches were collapsed if minimum length was zero.

Based on the error-wiped pedigrees from Category 1, MERLIN was used to generate 1000 replicates of simulated genotype data under the null hypothesis of no linkage, applying the same marker map, allele frequencies, LD-corrected cluster definitions and haplotype frequencies (generated from the original scan with the, cfreq option), and missing data pattern as the actual data.