SINGER stands for Sampling and INference of GEnealogies with Recombination, and it is a Bayesian method to do posterior sampling of Ancestral Recombination Graph under Sequentially Markovian Coalescent. SINGER works by iterative threading one haplotype to the partially-built ARG, until the ARG for all haplotypes have been built. After initialization, MCMC will be performed to update the ARG to explore the posterior distribution. For a full description and cite our method, you can check: Deng, Yun, Rasmus Nielsen, and Yun S. Song. "Robust and accurate bayesian inference of genome-wide genealogies for large samples." bioRxiv (2024): 2024-03.
Here we maintained the version which is under active development, but you can still direclty download the binary files for all past versions.
[We are temporarily providing beta versions of it, the official versions will be released when the preprint has been accepted for publication. You are welcome to use it, and submit bug reports at GitHub Issues. ]
If you want to compile the source files, then C++17 and cmake are required. Otherwise you can also used the pre-compiled binary files on various platforms.
The easiser way is to directory go to the folder releases/ and download one of the versions which work for your working platform (Linux/MacOS_Intel/MacOS_M1). After downloading, you can decompress it using:
tar -xvzf file_name
SINGER takes .vcf file and outputs a .trees file in tskit format. The mutations are already mapped to the branches, but non-polymorphic, multi-allelic sites and structral variants are excluded from inference. The branch length should be interpreted with units of generations, for example, for homo sapiens, you would need multiply that by 28 to convert to units of years. There will also be a .log file for you to check the argument you ran, and the summary statistic in MCMC iterations.
To sample ARGs with SINGER, you can run command line like shown below.
IMPORTANT!:if you wish to get ARG for: (1) a long chromosome or (2) a series of regions, we have provided more support to help you (see the next section: Tools). If you think there are other specific job pipeline which many people might want to use, please contact us and we might add it!
path_to_singer/singer_master -m 1.25e-8
-vcf prefix_of_vcf_file -output prefix_of_output_file
-start 0 -end 1e6
This command is to get the ARG samples for a specific region in the vcf file. We specify the details of the arguments here (or you can simply type path_to_singer/singer_master to display similar information):
The required flags include (either -m or -mut_map has to be provided):
| flag | required? | details |
|---|---|---|
| -m | conditionally required | per base pair per generation mutation rate |
| -mut_map | conditionally required | name of the file describing the mutation rate landscape |
| -vcf | required | prefix of the input .vcf file name |
| -output | required | prefix of the output .trees file name |
| -start | required | start position of the region |
| -end | required | end position of the region |
The optional flags include:
| flag | required? | details |
|---|---|---|
| -Ne | optional | the diploid effective population size, which means the haploid effective population size will be 2*Ne |
| -ratio | optional | the ratio between recombination and mutation rate, default at 1 |
| -recomb_map | optional | name of the file describing the recombination rate landscape |
| -n | optional | the number of posterior samples, default at 100 |
| -thin | optional | the number of MCMC iterations between adjacent samples, default at 20 |
| -polar | optional | the probability of correct polarization, default at 0.5 for unpolarized data, please use 0.99 for polarized data |
The output files will be:
prefix_of_output_files_nodes_{i}.txt, prefix_of_output_files_branches_{i}.txt, prefix_of_output_files_muts_{i}.txt, prefix_of_output_files_recombs_{i}.txt
with i from 0 to num_samples - 1. We recommend converting these files to tree sequence format in tskit, with this function:
path_to_singer/convert_to_tskit -input prefix_of_arg_files -output prefix_of_tskit_files
-start start_index -end end_index -step step_size
This tool will convert ARG sample with index from start_index to end_index, with interval size step_size.
SINGER is an MCMC-based sampling algorithm. To examine the convergence of it we normally examine the traces of summary statistics, and we have found that 2 summary statistics are quite good at indicating the convergence of the SINGER MCMC: fit to the diversity landscape and number of non-uniquely-mapped sites, as used in the manuscript. We have provided a python script to calculate the traces for these 2 quantities:
python compute_traces.py
-prefix prefix_of_tree_sequence_file -m mutation_rate
-start_index index_start_sample -end_index index_terminal_sample
-output_filename output_trace_filename
The script will calculate the aforementioned two statistics for all samples with index between the start_index and the end_index, and they will be output as the the 2 columns in the output file. The fit to the diversity landscape and the number of non-uniquely-mapped sites typically drops with more iterations of the MCMC, and when they reach to a stable stage that is usually a good sign for convergence.
In the manuscript we used the coalescence ratio to find introgression signals, which is based on the distribution of pairwise coalescence times between one haplytype and others, in every 10kb genome windows. Here we provide a python script tools, to compute the pairwise coalescence times between one given haplotype (indiciated by leaf node index) and others, in a windowed fashion.
python compute_pairwise_coalescence_times.py
--trees_file tree_sequence_filename --leaf_index index_of_leaf_node
--interval_size size_of_genome_window --output_filename output_file_name
Each row in the output file stands for all the pairwise coalescence times between the input leaf node index and all others. The rows are in the order of the genome windows.
Often people would like to run the ARG inference method for the entire chromosome (or even the entire genome), and we have provided a python script parallel_singer to facilitate you to this end. It automatically handles parallelization for you and runs SINGER multi-threaded.
parallel_singer -Ne 2e4 -m 1.2e-8
This script will:
- Cut the genome into windows (default at 1Mb)
- Remove the windows of unsequenced regions (<5 variants in the window)
- Automatically parallelize running SINGER on these windows
- Convert the output to
.treesfiles withtskitformat
[this tool is still under development, and will be available soon]
Sometimes it is of interest to only look at certain regions on the genome (e.g. selection signals), and we have provided support for this with the python script multiple_windows_singer.py. It will automatically parallelize running SINGER on the regions you specify with a given .bed file.
Tips: we recommend having windows not too small nor too big. A window containing 500-5000 SNPs would be ideal.
python multiple_windows_singer.py
This script will:
- Index the vcf file for these specified windows
- Automatically parallelize running SINGER on these windows
- Convert the output to
.treesfiles withtskitformat
- By far the most common bug is caused by not choosing the -Ne, -m parameter so that you roughly have
$\pi=4\cdot N_e \cdot m$ . For example, some bioinformatics pipeline can remove polymorphic sites significantly. You'll have to either change (effective) mutation rate or effective population size. Another common case is centromeres with almost no sequenced sites, please make sure not to include such regions in SINGER;
- As a Bayesian sampling method, SINGER works best when you sample some ARGs from posterior, only using one single sample is NOT ideal. To this point, we highly encourage specifying -n, -thin flags. You can find how we run SINGER on real datasets on:
- It is of importance to carefully choose the parameters, such as -Ne, -m, and -ratio. We recommend first choosing the mutation rate m, and then based on average pairwise diversity (
$\pi=4\cdot N_e \cdot m$ ), you can decide the Ne parameter. If you are not super sure about the recombination rate, you can use the default ratio of 1. - Unfortunately for now we only support phased, high-quality genomes, and polymorphic sites with missingness will be excluded. We are working on incorporating missingness and unphased data in the near future. ARGweaver has better support in these regards.