diff --git a/template_analysis/batch_template.m b/template_analysis/batch_template.m
index 81bfa5c..4141276 100644
--- a/template_analysis/batch_template.m
+++ b/template_analysis/batch_template.m
@@ -19,9 +19,6 @@
 AP=setPemDropThreshold(AP,5');
 % Add autofluorescence back in after removing for compensation?
 AP=setUseAutoFluorescence(AP,false');
-% By default, analysis tries to fit constitutive to transformedť and non-transformedť components
-% If your distribution is more complex or less complex, you can change the number of components
-% AP=setNumGaussianComponents(AP,3);
 
 % Make a map of condition names to file sets
 stem1011 = '../example_assay/LacI-CAGop_';
@@ -50,7 +47,7 @@
 % Make output plots
 OS = OutputSettings('LacI-CAGop','','','plots');
 OS.FixedInputAxis = [1e4 1e10];
-plot_batch_histograms(results,sampleresults,OS,{'b','y','r'},CM);
+plot_batch_histograms(results,sampleresults,OS,{'b','y','r'});
 
 save('LacI-CAGop-batch.mat','AP','bins','file_pairs','OS','results','sampleresults');
 
diff --git a/template_analysis/plots/placeholder.txt b/template_analysis/plots/placeholder.txt
new file mode 100644
index 0000000..152f67e
--- /dev/null
+++ b/template_analysis/plots/placeholder.txt
@@ -0,0 +1 @@
+A placeholder to make sure the plots directory is here when checked out
diff --git a/template_analysis/plusminus_template.m b/template_analysis/plusminus_template.m
index df7aa8b..8d0ce1a 100755
--- a/template_analysis/plusminus_template.m
+++ b/template_analysis/plusminus_template.m
@@ -23,9 +23,6 @@
 AP=setPemDropThreshold(AP,5');
 % Add autofluorescence back in after removing for compensation?
 AP=setUseAutoFluorescence(AP,false');
-% By default, analysis tries to fit constitutive to “transformed” and “non-transformed” components
-% If your distribution is more complex or less complex, you can change the number of components
-% AP=setNumGaussianComponents(AP,3);
 
 % Make a map of the batches of plus/minus comparisons to test
 % This analysis supports two variables: a +/- variable and a "tuning" variable
diff --git a/template_analysis/transfercurve_template.m b/template_analysis/transfercurve_template.m
index f63be3b..cd32c96 100644
--- a/template_analysis/transfercurve_template.m
+++ b/template_analysis/transfercurve_template.m
@@ -25,9 +25,6 @@
 AP=setPemDropThreshold(AP,5');
 % Add autofluorescence back in after removing for compensation?
 AP=setUseAutoFluorescence(AP,false');
-% By default, analysis tries to fit constitutive to “transformed” and “non-transformed” components
-% If your distribution is more complex or less complex, you can change the number of components
-% AP=setNumGaussianComponents(AP,3);
 
 % Make a map of induction levels to file sets
 stem1011 = '../example_assay/LacI-CAGop_';
diff --git a/template_colormodel/CM120312.mat b/template_colormodel/CM120312.mat
index 1e7f397..850a592 100644
Binary files a/template_colormodel/CM120312.mat and b/template_colormodel/CM120312.mat differ
diff --git a/template_colormodel/make_color_model.m b/template_colormodel/make_color_model.m
index 7ba9d2c..b497c06 100644
--- a/template_colormodel/make_color_model.m
+++ b/template_colormodel/make_color_model.m
@@ -25,7 +25,7 @@
 channels{1} = Channel('FITC-A', 488, 515, 20);
 channels{1} = setPrintName(channels{1}, 'EYFP'); % Name to print on charts
 channels{1} = setLineSpec(channels{1}, 'y'); % Color for lines, when needed
-colorfiles{1} = [stem0312 'EYFP_P3.fcs']; % If there is only one channel, the color file is optional
+colorfiles{1} = [stem0312 'EYFP_P3.fcs'];
 
 channels{2} = Channel('PE-Tx-Red-YG-A', 561, 610, 20);
 channels{2} = setPrintName(channels{2}, 'mKate');
diff --git a/template_colormodel/plots/placeholder.txt b/template_colormodel/plots/placeholder.txt
new file mode 100644
index 0000000..152f67e
--- /dev/null
+++ b/template_colormodel/plots/placeholder.txt
@@ -0,0 +1 @@
+A placeholder to make sure the plots directory is here when checked out