20251213
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@ -14,3 +14,4 @@
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99.scripts/phyparts/
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.pueue.yml
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run.status
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!*/_description.md
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@ -7,4 +7,4 @@ This directory contains raw data used for analysis.
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- `clean_fastq` This folder contains cleaned FASTQ files after quality control.
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- `raw_fastq` This folder contains the original raw FASTQ files.
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- `sra` This folder contains SRA files downloaded from the NCBI database.
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- `sra.list` This file lists the SRA accession numbers for the datasets used in this project.
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- `sra.list` This file lists the SRA downloading links for the datasets used in this project.
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@ -31,7 +31,7 @@ astraltree = readnewick(astralfile);
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### Alternatively, reading in the input files from Bucky
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### running in input_snaq/ folder
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inputCFfile = joinpath("..", "..", "input", "input.CFs.csv");
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inputCFfile = joinpath("bucky_1.CFs.csv");
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inputCF = readtableCF(inputCFfile);
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net0 = snaq!(astraltree, inputCF, hmax=0, filename="net0", seed=123, outgroup="Zju", runs=nruns);
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net1 = snaq!(net0, inputCF, hmax=1, filename="net1", seed=123, outgroup="Zju", runs=nruns);
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@ -60,7 +60,7 @@ rootatnode!(net4, "Zju");
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### rotate!(net4, -2);
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## Plotting the networks
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R"pdf"("snaq_networks.pdf", width=14, height=10);
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R"pdf"("snaq_networks_fulltree.pdf", width=14, height=10);
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R"layout(matrix(1:4, 2, 2, byrow=TRUE))"; # to get 4 plots into a single figure: 2 row, 2 columns
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R"par"(mar=[0, 0, 1.5, 0]); # for smaller margins
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xmin, xmax = PhyloPlots.PhyloPlots.edgenode_coordinates(net1, false, false)[13:14];
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@ -81,9 +81,52 @@ plot(net4, showgamma=true, tipoffset=0.1, xlim=[xmin, xmax]);
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R"mtext"(string("hmax=4, loglik=-", round(loglik(net4), digits=2)), font=2);
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R"dev.off"();
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R"pdf"("snaq_networks_majortree.pdf", width=14, height=10);
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R"layout(matrix(1:4, 2, 2, byrow=TRUE))"; # to get 4 plots into a single figure: 2 row, 2 columns
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R"par"(mar=[0, 0, 1.5, 0]); # for smaller margins
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xmin, xmax = PhyloPlots.PhyloPlots.edgenode_coordinates(net1, false, false)[13:14];
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xmax += (xmax - xmin) * 0.3;
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plot(net1, style=:majortree, showgamma=true, tipoffset=0.1, xlim=[xmin, xmax]);
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R"mtext"(string("hmax=1, loglik=-", round(loglik(net1), digits=2)), font=2);
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xmin, xmax = PhyloPlots.PhyloPlots.edgenode_coordinates(net2, false, false)[13:14];
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xmax += (xmax - xmin) * 0.3;
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plot(net2, style=:majortree, showgamma=true, tipoffset=0.1, xlim=[xmin, xmax]);
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R"mtext"(string("hmax=2, loglik=-", round(loglik(net2), digits=2)), font=2);
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xmin, xmax = PhyloPlots.PhyloPlots.edgenode_coordinates(net3, false, false)[13:14];
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xmax += (xmax - xmin) * 0.3;
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plot(net3, style=:majortree, showgamma=true, tipoffset=0.1, xlim=[xmin, xmax]);
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R"mtext"(string("hmax=3, loglik=-", round(loglik(net3), digits=2)), font=2);
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xmin, xmax = PhyloPlots.PhyloPlots.edgenode_coordinates(net4, false, false)[13:14];
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xmax += (xmax - xmin) * 0.3;
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plot(net4, style=:majortree, showgamma=true, tipoffset=0.1, xlim=[xmin, xmax]);
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R"mtext"(string("hmax=4, loglik=-", round(loglik(net4), digits=2)), font=2);
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R"dev.off"();
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## expected vs. observed quartet concordance factors
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using CSV, DataFrames;
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using CSV, DataFrames, Distributions, Random, RCall;
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inputCFfile = joinpath("bucky_1.CFs.csv");
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inputCF = readtableCF(inputCFfile);
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net3 = readsnaqnetwork("net3.out");
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topologymaxQpseudolik!(net3, inputCF);
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df_long = fittedquartetCF(inputCF, :long);
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### Adding jitter to the points for better visualization
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Random.seed!(123);
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jitter = 0.005;
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df_jittered = deepcopy(df_long);
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df_jittered.obsCF .+= rand(Uniform(-jitter / 2, jitter / 2), nrow(df_long));
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df_jittered.expCF .+= rand(Uniform(-jitter / 2, jitter / 2), nrow(df_long));
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R"pdf"("expCFs_obsvsfitted.pdf", width=6, height=6);
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R"plot"(df_jittered.obsCF, df_jittered.expCF, xlab="quartet CF observed in gene trees",
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ylab="quartet CF expected from network", pch=16,
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col="#008080",
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cex=0.7);
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R"abline"(0, 1, col="#008080", lwd=0.5);
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R"dev.off"();
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# Goodness of fit of the SNaQ networks
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using QuartetNetworkGoodnessFit;
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res1 = quarnetGoFtest!(net3, inputCF, true; seed=123, nsim=1000);
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res1[[1,2,3]] # p-value, uncorrected z, σ
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