Skip to content

Forward Regression framework to model substitution probabilities for 7-mer sequence context model, as described in Aggarwala and Voight (2015).

License

Notifications You must be signed in to change notification settings

bvoight/mutvar_fwdRegr

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 

History

32 Commits
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Repository files navigation

mutvar_fwdRegr

This repo contains the forward Regression framework used to model substitution probabilities for 7-mer sequence context model, as described in Aggarwala and Voight (2015).

Programs last tested:

	R (v3.3.2)
	Perl (v5.10.1)

R libraries:

	DAAG (1.20)
	lattice (0.20-34)
	leaps (2.9)
	latticeExtra (0.6-26)
	RColorBrewer (1.1-2)
	grid (3.3.2)

This may still be compatable with updated versions of these packages - but I have not tested with them!

Objectives

Explaining variability in substitution model (CpG/nonCpG) contexts via forward regression analysis

Round 2, update to capture removal of refseq and 1000G masked regions

By: BF Voight

Initially Created: 12.15.2014

Aim here is to take sequence context rates inferred from Varun's 7mer model specifically looking at frequent substitutions in non-CpG contexts -- specifically C-T and A-G) -- and develop a set of features which explain low/high variability

ideally, the broad hypothesis is that variability in rates of polymorphism within these contexts depend on some unknown biological mechanism(s), but that these are determined in part by the sequence context

This README (pipeline) is broken down into several parts

  1. Data Processing, creation of input files based on raw substitution probability tables
  2. Model and Feature Selection
  3. Making summary tables for features selected (e.g. Suppl. Table 7a, 7b)
  4. "Decoding" the sequence annotation (binary 0/1 encoding to A/C/G/T nucleotides)
  5. outputting "directional consistency" across different substitution classes
  6. output predicted values for models (example being C-T in CpG context)

1. Data Processing

On the RAW data file:

raw_data/ben_data_7mer_bayesian_test_training_AFR_10

This file contains a set of substitution probabilities:

  • for each type of substitution class
  • for each 7-mer sequence context
  • either for all chromosomes (autosome_rate), even chromosomes (training) and odd chromosomes (testing).
  • estimated using the AFR continental group, excluding admixed samples, described in Aggarwala and Voight (2015).
wc raw_data/ben_data_7mer_bayesian_test_training_AFR_10
  24579  147462 1879666 ben_data_7mer_bayesian_test_training_AFR_10

This matches (expected # of contexts is (4^7 * 3)/2 = 24576

  • (+1 header line: the header)
  • (+2 header line: which chromosomes selected for training/testing)

Now, run script to process all substitution classes

usage: %> rate_processor.pl [AC|AG|AT|CA|CG|CT] 
       	  		    [0|1|2]       
       			    raw_data/ben_data_7mer_bayesian_test_training_AFR_10 
			    ratefiles

arg 1: The substitution class of interest
arg 2: the CpG Flag (set 0 if desire AC|AG|AT; set =1 if desire CA|CG|CT -ve CpG context, 
       set =2 if desire CA|CG|CT +ve CpG context)
arg 3: the substitution probability table
arg 4: the directory to output the summary results files
### A to C/G/T substitutions [CpG = FALSE]
./rate_processor.pl AC 0 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl AG 0 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl AT 0 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles

### C to A/G/T substitutions [CpG = FALSE]
./rate_processor.pl CA 1 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl CG 1 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl CT 1 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles

### C to A/G/T substitutions [CpG = TRUE]
./rate_processor.pl CA 2 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl CG 2 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles
./rate_processor.pl CT 2 raw_data/ben_data_7mer_bayesian_test_training_AFR_10 ratefiles

Next, make the input files for R

usage: %>mk_nonCpG_covfile [A-G|C-T] ratefilesdir
usage: %>mk_CpG_covfile.pl [C-T|C-A|C-G] ratefilesdir

arg 1: The substitution class of interest: A-C, A-G, A-T, C-A, C-T, C-G
arg 2: the directory to output the summary results files.
./mk_nonCpG_covfile.pl A-C ratefiles
./mk_nonCpG_covfile.pl A-G ratefiles
./mk_nonCpG_covfile.pl A-T ratefiles
./mk_nonCpG_covfile.pl C-A ratefiles
./mk_nonCpG_covfile.pl C-T ratefiles
./mk_nonCpG_covfile.pl C-G ratefiles

./mk_CpG_covfile.pl C-A ratefiles
./mk_CpG_covfile.pl C-G ratefiles
./mk_CpG_covfile.pl C-T ratefiles

2. Model / Feature Selection

I've provide a listing of models given in the modelfiles directory.

If you looked at one of those files, e.g.

head -n 20 modelfiles/CVsel_1_2wayALL

p1_t1
p1_t2
p1_t3
p2_t1
p2_t2
p2_t3
p3_t1
p3_t2
p3_t3
p5_t1
p5_t2
p5_t3
p6_t1
p6_t2
p6_t3
p7_t1
p7_t2
p7_t3
p2_t1*p3_t1
p6_t3*p7_t3
...

To remind you of how the model is encoded: Each position (pX) is defined by three variables (tY), which then defined the nucleotide state for each position of the sequence context. You might ask "couldn't you code this with two variables?" Write it out - you'll see that the T state is "1 1" which is not quite what you want.

The nomenclature I'm using here is:

  • pX - where X is 1,2,3 or 5,6,7 - this is the position of the nucletoide sequence context
  • tY - where Y is 1,2 or 3 - this denotes the "label" for the nucleotide at the position
  • pX_tY*pX_tY - this denotes an 'interaction' term of the given position/nucleotide.

I've encoded this as (arbitarily) as:

0 0 0 = A
0 0 1 = C
0 1 0 = G
1 0 0 = T

which means the "reference" nucleotide is "A", i.e., the change in probability of substitution which is estimated is change (C, G, or T) relative To A.

Note that you can have multiple interactions (here, 2way, but 3 or 4 way, for example). The modelfiles will give the list all of these possible interactions

Finally, for specific models that fix CpG context, this means that p5 is always set to "G". in that case, you don't need to include this as a variable, and there will be no interaction terms possible with that position, i.e., the model space is 'reduced'. I have provided those listings for you.

And obviously, p4 is excluded since that is the position of the polymorphic site, and in our case, we're stratifying each substitution classes of which there are 9: A-C, A-G, A-T, C-A, C-G, C-T (non-CpG), and C-A, C-G, C-T (CpG).

Note:

By default, the P-value threshold for the F-test significance test to add terms is set at P = 0.001.

If you want to change this to something more strict (more significant P-value leading to fewer features selected) or less strict (leading to more features selected), you would need to edit the script auto_finalmodel_CV.pl script and change $sig_th = 0.01; to any p-value you desire.

Yes, I realize the how ugly this is. Bad Coder, no Doughnut!! I apologize -- it's what happens when the PI has to code with limited time. :/

For what it's worth, I've set this to something less strict (P=0.01) and qualitatively find similar results for 7-mer modelling purposes.

usage: %> auto_finalmodel_CV.pl [0|1|2] [A-C|A-G|A-T|C-A|C-G|C-T] path ratefiledir modelpath

arg 1: CpG Flag: =2 if CA,CG,CT in CpG is desired, =1 if CA,CG,CT if non-CpG is desired, =0 if AC,AG,AT is desired
arg 2: the directory in which to store the results [e.g., 00_AC for AC; 01_CT for CT in CpG, etc.]
arg 3: path where ratefiles are stored
arg 4: path where modelfiles are stored 

This is a master script which:

  1. calls model_picker.R in R, which is the unit that performs the actual feature selection steps.

This script performs the series of feature selection steps in turn, e.g. 0 interactions, 2-way, 3-way, then 4-way interactions.

This uses the training rate files to build the model out.

This script also maintains the "hierarchy of constraint": when adding increasingly complex interactions (i.e., 3-way), if the lower order terms are not present (2-way, 1-way), it will add those, increase the degree of freedom, and performs the F-test with the increased number of additional parameters (and higher df's)

  1. calls auto_CVsummary.pl, which performs the cross validation and summary analysis automatically for all models developed.

this script calls mutRate_CV_summary.R in R, which is the unit that perform the actual cross validation experiments.

Here, 8-fold CV is performed.

# Run model and feature building.
./auto_finalmodel_CV.pl 2 C-A 01_CA ratefiles modelfiles
./auto_finalmodel_CV.pl 2 C-G 01_CG ratefiles modelfiles
./auto_finalmodel_CV.pl 2 C-T 01_CT ratefiles modelfiles

./auto_finalmodel_CV.pl 1 C-A 00_CA ratefiles modelfiles
./auto_finalmodel_CV.pl 1 C-G 00_CG ratefiles modelfiles
./auto_finalmodel_CV.pl 1 C-T 00_CT ratefiles modelfiles

./auto_finalmodel_CV.pl 0 A-C 00_AC ratefiles modelfiles
./auto_finalmodel_CV.pl 0 A-G 00_AG ratefiles modelfiles
./auto_finalmodel_CV.pl 0 A-T 00_AT ratefiles modelfiles

Output are placed in the specified output directory (e.e., 00_AC, 00_AG, etc.).

File output produced: (X and Y are placeholders for nucleotides, e.g. C-A or C-T or A-C, etc.)

*.Rout: raw output from the given model_picker.R run

CVsel_*way_X-Y.CVout: Text file for the summary output results for cross validation (training phase) and results for holdout (testing phase) including ALL features

tryit_*way: the list of selected feature for the given interaction model (1way, 2way, 3way, or 4way). Format similar to files found in modelfile directory

tryit_*way_X-Y.CVout: Text file for the summary output results for cross validation (training phase) and results for holdout (testing phase) including the subset of selected features

modellist_X-Y: the list of all models that will be tested in cross validation

3. Making summary tables for features selected (e.g. Suppl. Table 7a, 7b)

usage: %> R --vanilla <output_allmodels.R --args paramfile datafile outfile

arg 1 [paramfile]: a lists of features from the model (ie., "tryit_4way")
arg 2 [datafile]: the rate file to incorporate (i.e., ratefiles/*_all_cov_vf.txt)
arg 3 [outfile]: the path of the output file that is generated. 

Format for the output file is:

PARAM BETA SE TVAL PVAL
(Intercept) 0.119725606572481 0.00133737269238609 89.5229932943157 0
p1_t1 0.00299726083766459 0.00135540478491911 2.21134001518481 0.0272734178496301
p1_t2 -0.000284399681618097 0.00108345427233726 -0.262493479309082 0.793003586043526
...

col 1: the parameter/feature (encoded)
col 2: the output effect size (BETA) from the regression
col 3: the statistic for the final regression including this 
       feature (in the context of all provided featuers)
col 4: the associated p-value for the statstic from the final 
       regression including this feature (in the context of all provided features)
## nonCpG
R --vanilla <output_allmodels.R --args 00_AC/tryit_4way ratefiles/nonCpG_rates_A-C_all_cov_vf.txt \
  	    00_AC/nCpG_A-C_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_AC/tryit_4way ratefiles/nonCpG_rates_A-C_train_cov_vf.txt \
  	    00_AC/nCpG_A-C_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_AC/tryit_4way ratefiles/nonCpG_rates_A-C_test_cov_vf.txt \
  	    00_AC/nCpG_A-C_modelsum_test.txt

R --vanilla <output_allmodels.R --args 00_AG/tryit_4way ratefiles/nonCpG_rates_A-G_all_cov_vf.txt \
  	    00_AG/nCpG_A-G_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_AG/tryit_4way ratefiles/nonCpG_rates_A-G_train_cov_vf.txt \
  	    00_AG/nCpG_A-G_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_AG/tryit_4way ratefiles/nonCpG_rates_A-G_test_cov_vf.txt \
  	    00_AG/nCpG_A-G_modelsum_test.txt

R --vanilla <output_allmodels.R --args 00_AT/tryit_4way ratefiles/nonCpG_rates_A-T_all_cov_vf.txt \
  	    00_AT/nCpG_A-T_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_AT/tryit_4way ratefiles/nonCpG_rates_A-T_train_cov_vf.txt \
  	    00_AT/nCpG_A-T_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_AT/tryit_4way ratefiles/nonCpG_rates_A-T_test_cov_vf.txt \
  	    00_AT/nCpG_A-T_modelsum_test.txt

R --vanilla <output_allmodels.R --args 00_CA/tryit_4way ratefiles/nonCpG_rates_C-A_all_cov_vf.txt \
  	    00_CA/nCpG_C-A_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_CA/tryit_4way ratefiles/nonCpG_rates_C-A_train_cov_vf.txt \
  	    00_CA/nCpG_C-A_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_CA/tryit_4way ratefiles/nonCpG_rates_C-A_test_cov_vf.txt \
  	    00_CA/nCpG_C-A_modelsum_test.txt

R --vanilla <output_allmodels.R --args 00_CG/tryit_4way ratefiles/nonCpG_rates_C-G_all_cov_vf.txt \
  	    00_CG/nCpG_C-G_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_CG/tryit_4way ratefiles/nonCpG_rates_C-G_train_cov_vf.txt \
  	    00_CG/nCpG_C-G_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_CG/tryit_4way ratefiles/nonCpG_rates_C-G_test_cov_vf.txt \
  	    00_CG/nCpG_C-G_modelsum_test.txt

R --vanilla <output_allmodels.R --args 00_CT/tryit_4way ratefiles/nonCpG_rates_C-T_all_cov_vf.txt \
  	    00_CT/nCpG_C-T_modelsum_all.txt
R --vanilla <output_allmodels.R --args 00_CT/tryit_4way ratefiles/nonCpG_rates_C-T_train_cov_vf.txt \
  	    00_CT/nCpG_C-T_modelsum_train.txt
R --vanilla <output_allmodels.R --args 00_CT/tryit_4way ratefiles/nonCpG_rates_C-T_test_cov_vf.txt \
  	    00_CT/nCpG_C-T_modelsum_test.txt

## CpG
######NOTE: for this substitution class (C-A), the best model was 
	    "all first + 2 way via feature selection" (tryit_2way)
R --vanilla <output_allmodels.R --args 01_CA/tryit_2way ratefiles/CpG_rates_C-A_all_cov_vf.txt \
  	    01_CA/CpG_C-A_modelsum_all.txt
R --vanilla <output_allmodels.R --args 01_CA/tryit_2way ratefiles/CpG_rates_C-A_train_cov_vf.txt \
  	    01_CA/CpG_C-A_modelsum_train.txt
R --vanilla <output_allmodels.R --args 01_CA/tryit_2way ratefiles/CpG_rates_C-A_test_cov_vf.txt \
  	    01_CA/CpG_C-A_modelsum_test.txt

R --vanilla <output_allmodels.R --args 01_CG/tryit_4way ratefiles/CpG_rates_C-G_all_cov_vf.txt \
  	    01_CG/CpG_C-G_modelsum_all.txt
R --vanilla <output_allmodels.R --args 01_CG/tryit_4way ratefiles/CpG_rates_C-G_train_cov_vf.txt \
  	    01_CG/CpG_C-G_modelsum_train.txt
R --vanilla <output_allmodels.R --args 01_CG/tryit_4way ratefiles/CpG_rates_C-G_test_cov_vf.txt \
  	    01_CG/CpG_C-G_modelsum_test.txt

R --vanilla <output_allmodels.R --args 01_CT/tryit_4way ratefiles/CpG_rates_C-T_all_cov_vf.txt \
  	    01_CT/CpG_C-T_modelsum_all.txt
R --vanilla <output_allmodels.R --args 01_CT/tryit_4way ratefiles/CpG_rates_C-T_train_cov_vf.txt \
  	    01_CT/CpG_C-T_modelsum_train.txt
R --vanilla <output_allmodels.R --args 01_CT/tryit_4way ratefiles/CpG_rates_C-T_test_cov_vf.txt \
  	    01_CT/CpG_C-T_modelsum_test.txt

CONFIRMED! reproduces to this point at least for: C-T CpGs, A-T, and C-T non-CpG.

4. "Decoding" the sequence annotation (binary 0/1 encoding to A/C/G/T nucleotides)

This script takes output from the output_allmodel.R script (i.e., *modelsum_*.txt, above) reads the PARAM column, and appends a new column with interprets the sequence context (given the previous coding listed above):

./R_param_decoder.pl <00_AC/nCpG_A-C_modelsum_all.txt >00_AC/nCpG_A-C_modelsum_all_bpseq.txt
./R_param_decoder.pl <00_AG/nCpG_A-G_modelsum_all.txt >00_AG/nCpG_A-G_modelsum_all_bpseq.txt
./R_param_decoder.pl <00_AT/nCpG_A-T_modelsum_all.txt >00_AT/nCpG_A-T_modelsum_all_bpseq.txt
./R_param_decoder.pl <00_CA/nCpG_C-A_modelsum_all.txt >00_CA/nCpG_C-A_modelsum_all_bpseq.txt
./R_param_decoder.pl <00_CG/nCpG_C-G_modelsum_all.txt >00_CG/nCpG_C-G_modelsum_all_bpseq.txt
./R_param_decoder.pl <00_CT/nCpG_C-T_modelsum_all.txt >00_CT/nCpG_C-T_modelsum_all_bpseq.txt
./R_param_decoder.pl <01_CA/CpG_C-A_modelsum_all.txt >01_CA/CpG_C-A_modelsum_all_bpseq.txt
./R_param_decoder.pl <01_CG/CpG_C-G_modelsum_all.txt >01_CG/CpG_C-G_modelsum_all_bpseq.txt
./R_param_decoder.pl <01_CT/CpG_C-T_modelsum_all.txt >01_CT/CpG_C-T_modelsum_all_bpseq.txt

./R_param_decoder.pl <00_AC/nCpG_A-C_modelsum_train.txt >00_AC/nCpG_A-C_modelsum_train_bpseq.txt
./R_param_decoder.pl <00_AG/nCpG_A-G_modelsum_train.txt >00_AG/nCpG_A-G_modelsum_train_bpseq.txt
./R_param_decoder.pl <00_AT/nCpG_A-T_modelsum_train.txt >00_AT/nCpG_A-T_modelsum_train_bpseq.txt
./R_param_decoder.pl <00_CA/nCpG_C-A_modelsum_train.txt >00_CA/nCpG_C-A_modelsum_train_bpseq.txt
./R_param_decoder.pl <00_CG/nCpG_C-G_modelsum_train.txt >00_CG/nCpG_C-G_modelsum_train_bpseq.txt
./R_param_decoder.pl <00_CT/nCpG_C-T_modelsum_train.txt >00_CT/nCpG_C-T_modelsum_train_bpseq.txt
./R_param_decoder.pl <01_CA/CpG_C-A_modelsum_train.txt >01_CA/CpG_C-A_modelsum_train_bpseq.txt
./R_param_decoder.pl <01_CG/CpG_C-G_modelsum_train.txt >01_CG/CpG_C-G_modelsum_train_bpseq.txt
./R_param_decoder.pl <01_CT/CpG_C-T_modelsum_train.txt >01_CT/CpG_C-T_modelsum_train_bpseq.txt

./R_param_decoder.pl <00_AC/nCpG_A-C_modelsum_test.txt >00_AC/nCpG_A-C_modelsum_test_bpseq.txt
./R_param_decoder.pl <00_AG/nCpG_A-G_modelsum_test.txt >00_AG/nCpG_A-G_modelsum_test_bpseq.txt
./R_param_decoder.pl <00_AT/nCpG_A-T_modelsum_test.txt >00_AT/nCpG_A-T_modelsum_test_bpseq.txt
./R_param_decoder.pl <00_CA/nCpG_C-A_modelsum_test.txt >00_CA/nCpG_C-A_modelsum_test_bpseq.txt
./R_param_decoder.pl <00_CG/nCpG_C-G_modelsum_test.txt >00_CG/nCpG_C-G_modelsum_test_bpseq.txt
./R_param_decoder.pl <00_CT/nCpG_C-T_modelsum_test.txt >00_CT/nCpG_C-T_modelsum_test_bpseq.txt
./R_param_decoder.pl <01_CA/CpG_C-A_modelsum_test.txt >01_CA/CpG_C-A_modelsum_test_bpseq.txt
./R_param_decoder.pl <01_CG/CpG_C-G_modelsum_test.txt >01_CG/CpG_C-G_modelsum_test_bpseq.txt
./R_param_decoder.pl <01_CT/CpG_C-T_modelsum_test.txt >01_CT/CpG_C-T_modelsum_test_bpseq.txt

Create a merged, master file

#nCpG
./mutsum_mergeem.pl 00_AC/nCpG_A-C_modelsum_all_bpseq.txt \
                    00_AG/nCpG_A-G_modelsum_all_bpseq.txt \
                    00_AT/nCpG_A-T_modelsum_all_bpseq.txt \
                    00_CA/nCpG_C-A_modelsum_all_bpseq.txt \
                    00_CG/nCpG_C-G_modelsum_all_bpseq.txt \
                    00_CT/nCpG_C-T_modelsum_all_bpseq.txt \
                    >finaltables/nCpG_sorted_featuretable_all.txt

./mutsum_mergeem.pl 00_AC/nCpG_A-C_modelsum_train_bpseq.txt \
                    00_AG/nCpG_A-G_modelsum_train_bpseq.txt \
                    00_AT/nCpG_A-T_modelsum_train_bpseq.txt \
                    00_CA/nCpG_C-A_modelsum_train_bpseq.txt \
                    00_CG/nCpG_C-G_modelsum_train_bpseq.txt \
                    00_CT/nCpG_C-T_modelsum_train_bpseq.txt \
                    >finaltables/nCpG_sorted_featuretable_train.txt

./mutsum_mergeem.pl 00_AC/nCpG_A-C_modelsum_test_bpseq.txt \
                    00_AG/nCpG_A-G_modelsum_test_bpseq.txt \
                    00_AT/nCpG_A-T_modelsum_test_bpseq.txt \
                    00_CA/nCpG_C-A_modelsum_test_bpseq.txt \
                    00_CG/nCpG_C-G_modelsum_test_bpseq.txt \
                    00_CT/nCpG_C-T_modelsum_test_bpseq.txt \
                    >finaltables/nCpG_sorted_featuretable_test.txt

## CpG
./mutsum_mergeem.pl 01_CA/CpG_C-A_modelsum_all_bpseq.txt \
                    01_CG/CpG_C-G_modelsum_all_bpseq.txt \
                    01_CT/CpG_C-T_modelsum_all_bpseq.txt \
                    >finaltables/CpG_sorted_featuretable_all.txt

./mutsum_mergeem.pl 01_CA/CpG_C-A_modelsum_train_bpseq.txt \
                    01_CG/CpG_C-G_modelsum_train_bpseq.txt \
                    01_CT/CpG_C-T_modelsum_train_bpseq.txt \
                    >finaltables/CpG_sorted_featuretable_train.txt

/mutsum_mergeem.pl 01_CA/CpG_C-A_modelsum_test_bpseq.txt \
                    01_CG/CpG_C-G_modelsum_test_bpseq.txt \
                    01_CT/CpG_C-T_modelsum_test_bpseq.txt \
                    >finaltables/CpG_sorted_featuretable_test.txt

5. outputting "directional consistency" across different substitution classes

#append directional consistency
./mutsum_dirconst.pl <finaltables/nCpG_sorted_featuretable_all.txt \
		     >finaltables/nCpG_sorted_featuretable_all_wdir.txt
./mutsum_dirconst.pl <finaltables/nCpG_sorted_featuretable_train.txt \
		     >finaltables/nCpG_sorted_featuretable_train_wdir.txt
./mutsum_dirconst.pl <finaltables/nCpG_sorted_featuretable_test.txt \
		     >finaltables/nCpG_sorted_featuretable_test_wdir.txt

./mutsum_dirconst.pl <finaltables/CpG_sorted_featuretable_all.txt \
		     >finaltables/CpG_sorted_featuretable_all_wdir.txt
./mutsum_dirconst.pl <finaltables/CpG_sorted_featuretable_train.txt \
		     >finaltables/CpG_sorted_featuretable_train_wdir.txt
./mutsum_dirconst.pl <finaltables/CpG_sorted_featuretable_test.txt \
		     >finaltables/CpG_sorted_featuretable_test_wdir.txt
#extract final columns and report tables
awk -F ' ' ' {print($1,$2,$3,$5,$7,$9,$11,$13,$15)} ' <finaltables/nCpG_sorted_featuretable_all_wdir.txt \
       >finaltables/nCpG_featuretable_all_vf.txt
awk -F ' ' ' {print($1,$2,$3,$5,$7,$9,$11,$13,$15)} ' <finaltables/nCpG_sorted_featuretable_all_wdir.txt \
    >finaltables/nCpG_featuretable_train_vf.txt
awk -F ' ' ' {print($1,$2,$3,$5,$7,$9,$11,$13,$15)} ' <finaltables/nCpG_sorted_featuretable_all_wdir.txt \
    >finaltables/nCpG_featuretable_test_vf.txt

awk -F ' ' ' {print($1,$2,$3,$5,$7,$9)} ' <finaltables/CpG_sorted_featuretable_all_wdir.txt \
    >finaltables/CpG_featuretable_all_vf.txt
awk -F ' ' ' {print($1,$2,$3,$5,$7,$9)} ' <finaltables/CpG_sorted_featuretable_all_wdir.txt \
    >finaltables/CpG_featuretable_train_vf.txt
awk -F ' ' ' {print($1,$2,$3,$5,$7,$9)} ' <finaltables/CpG_sorted_featuretable_all_wdir.txt \
    >finaltables/CpG_featuretable_test_vf.txt

6. output predicted values for models (example being C-T in CpG context)

#command line called:

R --vanilla --args 01_CT/tryit_4way 
  	    	   ratefiles/CpG_rates_C-T_train_cov_vf.txt 
		   ratefiles/CpG_rates_C-T_test_cov_vf.txt 
		   CpG_C-T_train_predictRates.txt
#R code here for above command: 
library(DAAG);
source("mutRate_intx.R");
args <- commandArgs();

paramfile <- args[4];
datafile_train <- args[5];
datafile_test <- args[6];
outfile <- args[7];

tr <- read.table(file=datafile_train,header=T)
ts <- read.table(file=datafile_test,header=T)
x <- tr[order(tr[,2]),]
tr <- x
x <- ts[order(ts[,2]),]
ts <- x
form <- intx_makeformula(paramfile,"",flag=0);
reg <- lm(form, data=tr);

pred_tr <- cbind(as.character(tr$SEQ_REF), predict(reg,interval=c("prediction")));
write.table(pred_tr[,1:2],file=outfile,quote=F,row.names=F, col.names=F)

About

Forward Regression framework to model substitution probabilities for 7-mer sequence context model, as described in Aggarwala and Voight (2015).

Resources

License

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published

Languages