19 EM Haplotype Frequency Estimation
19.1 Haplotype Frequency Estimation Overview
19.2 Window Display and Navigation
19.2.1 Marker List
19.2.2 Patient List
19.2.3 Alternate Field Chooser
19.2.4 Haplotype List
19.2.5 Copying Haplotype Results
19.2.6 EM Initial Conditions
19.2.7 Compute EM/Refine Estimate
19.2.8 Finish EM
19.2.9 Refine Estimate
19.2.10 Re-Compute
19.2.11 Initialize
19.2.12 Step Once
19.2.13 Display Threshold
19.2.14 Reshow
19.2.15 Confidence Interval Estimation Threshold
19.2.16 Use Patient Data Containing Missing Values
19.2.17 Maximum EM Iterations
19.2.18 EM Convergence Tolerance
19.2.19 Genotypes/Haplotypes
19.2.20 Haplotypes Shown
19.2.21 Current EM Iterations
19.2.22 Proximity to Convergence
19.3 Example of Using the Patient List
19.4 EM Table and CHM Table
19.5 The Diplotype Table
19.2 Window Display and Navigation
19.2.1 Marker List
19.2.2 Patient List
19.2.3 Alternate Field Chooser
19.2.4 Haplotype List
19.2.5 Copying Haplotype Results
19.2.6 EM Initial Conditions
19.2.7 Compute EM/Refine Estimate
19.2.8 Finish EM
19.2.9 Refine Estimate
19.2.10 Re-Compute
19.2.11 Initialize
19.2.12 Step Once
19.2.13 Display Threshold
19.2.14 Reshow
19.2.15 Confidence Interval Estimation Threshold
19.2.16 Use Patient Data Containing Missing Values
19.2.17 Maximum EM Iterations
19.2.18 EM Convergence Tolerance
19.2.19 Genotypes/Haplotypes
19.2.20 Haplotypes Shown
19.2.21 Current EM Iterations
19.2.22 Proximity to Convergence
19.3 Example of Using the Patient List
19.4 EM Table and CHM Table
19.5 The Diplotype Table
