CALDER (Cancer Analysis of Longitudinal Data through Evolutionary Reconstruction) is an algorithm for inferring evolutionary phylogenies using multiple longitudinal bulk DNA sequencing samples from the same patient. CALDER improves upon previous methods by enforcing the evolutionary relationships that are expected between temporally ordered samples.
The setup process for CALDER requires the following steps:
The following command clones the current CALDER repository from GitHub:
git clone https://github.com/raphael-group/calder.git
The following software is required for CALDER:
- Linux/Unix or Windows
- Java 8 Runtime Environment (JRE)
- ILP solver (see below)
- Optional: Absence-Aware Clustering to cluster mutations.
With the dependencies set up correctly, the following command will run CALDER on the provided test input and write the results to a subdirectory called "output":
java -jar calder.jar -i CLL003_clustered.txt -o output
This should take no more than a few seconds to run and the output should match the contents of the sample_output folder.
CALDER has the following steps.
The input file is a tab-separated text file representing a matrix of read counts. Each row corresponds to a longitudinal sample, and alternating columns designate the reference reads and variant reads covering each mutation, respectively. For example, an instance with 3 samples and 4 mutations could be like so:
a a b b c c d d t1 700 300 0 0 0 0 0 0 t2 700 300 800 200 900 100 900 100 t3 600 400 800 200 900 100 900 100
For real datasets with a considerable number of mutations (more than 40), we recommend using Absence-Aware Clustering to cluster mutations.
CALDER assumes that input mutations are in copy-neutral regions, i.e., that the number of reads with a mutation is proportional to the number of cells with that mutation. If you suspect this assumption does not hold for your data, consider excluding mutations that may be affected by CNA; alternatively, if you have copy number calls (e.g., from HATCHet), you could correct the read counts to represent the true CCF.
The command to run CALDER is simply "java -jar calder.jar" followed by command line arguments. The option -i to designate the input file is required.
For each solution, CALDER produces 2 text files: a DOT file containing the inferred phylogenetic tree T, and a CSV file containing the inferred frequency matrix Fhat and the clone proportion matrix U. DOT files can be visualized using standard tools such as
graphviz (see below for an example), and the matrices in CSV format can also be manipulated using standard tools -- (see soln_to_timescape.py for an example that does so using the
pandas library in Python).
To visualize a tree using Graphviz (after installing it), you can navigate to the output directory and run the following command:
dot -Tpng CLL003_tree1.dot > CLL003_soln1.png
See the Graphviz documentation for more options.
We provide a script to support visualizing clone mixture proportions using the Timescape R package. This requires the following dependencies:
- Python 3
- Python packages:
- R >= 3.3
- R package: Timescape (and its dependencies)
First, run the Python script to convert the solution DOT and CSV files to Timescape-formatted files (assuming that
python refers to Python 3):
python soln_to_timescape.py outdir/CLL003_soln1.csv outdir/CLL003_tree1.dot CLL003
Then, run the following commands in R to generate the visualization:
library(timescape) prev <- read.table("CLL003_prev.txt", header=TRUE) edges <- read.table("CLL003_edges.txt", header=TRUE) timescape(clonal_prev = prev, tree_edges = edges)
See the Timescape documentation for more options.
We recommend clustering mutations by frequency before running CALDER - primarily because we generally expect to have multiple mutations distinguishing between any two clonal expansion events, and therefore between any two clones. We recommend using Absence-Aware Clustering, a clustering algorithm that pays particular attention to the distinction between mutation presence and absence. Python scripts are included to convert a CALDER input file to the format required by the clustering software, and to convert the clustering output back to CALDER input format.
- Absence-Aware Clustering (see the link for dependencies as well as instructions for installation and usage)
- Python 3
The following command converts CALDER-formatted input to clustering input (assuming that
python refers to Python 3):
python calder_to_clustering.py calder_input.txt clustering_input.txt
Then, after running Absence-Aware Clustering, use the following command to apply the cluster assignments to the original data (where
clustering_assignments.txt is the output file from the top level of the clustering output directory):
python apply_clustering.py calder_input.txt cluster_assignments.txt calder_input_clustered.txt
CALDER Command line options
Required -i,--input <arg> input file path -o,--output <arg> output directory Additional options -a,--alpha <arg> confidence level alpha (default 0.9) -h,--threshold <arg> detection threshold h (default 0.01) -O,--objective <arg> objective function (l0 or l1) -N,--nonlongitudinal do not enforce longitudinal constraints (for non-longitudinal data) -c,--printconf print effective confidence level -g,--print-graph print ancestry graph -n,--intervals print confidence intervals (default false) -s,--solutions <arg> maximum number of optimal solutions to return (default 1) -t,--time track and output timing information -v,--solver <arg> MILP solver back-end (default gurobi)
CALDER requires a specialized ILP solver. We recommend the Gurobi optimizer (version 8.0 required), as it is fast, easy to install, and supported on all platforms (website includes instructions for obtaining a license, downloading, and installing).
If for some reason you would prefer not to use Gurobi (e.g., if you are part of a non-academic entity and not interested in purchasing a license), we also support the GLPK solver with the GLPK for Java interface, or the lp-solve solver. We generally found GLPK to be faster and easier to use on all platforms. For more details, see the specific installation instructions for each solver. Installation tends to be easier on Linux systems than on Mac or Windows systems. Note that you will need to specify the alternate solver using the -v option.
For assistance with running CALDER, interpreting the results, or other related questions, please email me (Matt Myers) at this address: email@example.com
LICENSE for license information.
If you use CALDER in your work, please cite the following paper (available here):
Myers, M.A., Satas, G. and Raphael, B.J., 2019. CALDER: Inferring Phylogenetic Trees from Longitudinal Tumor Samples. Cell Systems.