autoStreamTree is a Python package meant for analysing genomic variants (e.g., SNPs, microhaplotypes) within geospatial network contexts, such as river systems or other dendritic environments. It provides a way to visualize reach- or segment- level contributions given a matrix of pairwise distances.
An input geospatial network (as shapefile, geodatabase, or .gpkg) is first used to compute a minimally representative graph structure for all least-cost paths between your sampling locations. Pairwise genomic distances (e.g., Fst) are then 'fitted' to this graph by calculating the contribution of each graph segment, using the least-squares algorithm from Kalinowsky et al. (2008), similarly to the manner used to fit branch lengths within a neighbor-joining phylogeny.
autoStreamTree automates what was previously a manual process, while also integrating new functionality such as per-locus or per-site fitted distances, which can be used for downstream outlier analysis.
autoStreamTree is a Python package which relies upon a number of dependencies:
- pandas
- numpy
- geopandas
- pyogrio
- matplotlib
- seaborn
- pyproj
- networkx
- scikit-learn
- momepy
- mantel
- pysam
- sortedcontainers
autoStreamTree also uses methodology described in Kalinowski et al. 2008, if you use this software you should cite:
Kalinowski ST, MH Meeuwig, SR Narum, ML Taper (2008) Stream trees: a statistical method for mapping genetic differences between populations of freshwater organisms to the sections of streams that connect them. Canadian Journal of Fisheries and Aquatic Sciences (65:2752-2760)
The recommended method of installation is with conda or mamba. First, create
and activate a new conda environment:
conda create -n streamtree python=3.10
conda activate streamtree
Then install the package:
mamba install -c ecoevoinfo -c conda-forge -c bioconda autostreamtree
If you require the development branch, you can then install from GitHub as
well:
git clone https://github.com/tkchafin/autostreamtree.git
cd autostreamtree
pip install .
You should now be ready to go!
Currently there are some dependencies which can't be easily installed on Macs running the Apple ARM CPU architectures. If you are using an Apple Silicon (M1/M2) Mac there are some extra steps to run x86_64 (Intel-based) applications, which you can do via Rosetta 2. Here are the steps to set up and launch a terminal in Rosetta mode:
-
Install Rosetta:
-
Open the Terminal app (found in
Applications>Utilities). -
Enter the following command and press Return:
/usr/sbin/softwareupdate --install-rosetta --agree-to-license -
If Rosetta is already installed, this command will have no effect. If it's not installed, you'll be prompted to agree to the license terms, and the installation will proceed.
-
-
Find Terminal in Finder:
- Open Finder.
- Navigate to the
Applicationsfolder, thenUtilities. - Find
Terminal.
-
Duplicate Terminal:
- Right-click (or Ctrl-click) on
Terminal. - Select
Duplicateto create a copy of the Terminal application. This ensures you have a separate instance for Rosetta without altering your default Terminal.
- Right-click (or Ctrl-click) on
-
Enable Rosetta for the Duplicated Terminal:
- Right-click (or Ctrl-click) on the duplicated Terminal.
- Select
Get Info. - In the
Infowindow, check the boxOpen using Rosetta.
-
Launch the Rosetta Terminal:
- Open the duplicated Terminal application. This instance of Terminal will run under Rosetta, allowing you to run x86_64 architecture applications.
Once this is done, you can create a conda environment:
conda create -n streamtree
conda activate streamtree
conda config --env --set subdir osx-64
conda install python=3.10
Then install autostreamtree:
conda install -c ecoevoinfo -c conda-forge -c bioconda autostreamtree
Docker images are also built and hosted for all releases on DockerHub. To run using the latest release:
docker run --platform linux/amd64 -it tkchafin/autostreamtree:latest
If you require a certain release, you can reference the tag by changing the image name like so:
docker run -it tkchafin/autostreamtree:v1.1.2
After installation, you can view the up-to-date help menu by calling the script with autostreamtree -h:
autostreamtree
Author: Tyler K Chafin, Biomathematics and Statistics Scotland
Description: Methods for analysing genetic distances in networks.
Mandatory arguments:
-s, --shp : Path to shapefile containing cleaned, contiguous stream reaches
(can also support geodatabase or GPKG files)
-i, --input : Input .tsv file containing sample coordinates
-v, --vcf : Input VCF file containing genotypes
General options:
-o, --out : Output prefix [default="out"]
-O, --gdf_out : Output driver for annotated geodataframe (options "SHP", "GPKG", "GDB")
-C, --concat : Concatenate all SNPs ("all"), by locus ("loc"), or not at all ("none")
-n, --network : Provide an already optimized network output from a previous run
--overwrite : Overwrite an input network (Only relevant with --network)
-h, --help : Displays help menu
-r, --run : Run which steps? Options:
ALL : Run all steps
GENDIST : Only calculate genetic distance matrix
STREAMDIST : Only compute pairwise stream distances
DISTANCES : Only compute GENDIST + STREAMDIST
IBD : GENDIST + STREAMDIST + Mantel test
STREAMTREE : GENDIST + STREAMDIST + fit StreamTree model
RUNLOCI : Run STREAMTREE fitting on each locus
-p, --pop : Pool individuals based on an input population map tsv file
NOTE: The location will be taken as the centroid among individual samples
-g, --geopop : Pool individuals having identical coordinates
-c, --clusterpop: Use DBSCAN algorithm to automatically cluster populations
--reachid_col : Attribute name representing primary key in shapefile [default="HYRIV_ID"]
--length_col : Attribute name giving length in kilometers [default="LENGTH_KM"]
--seed : Seed for RNG
Genetic distance options:
-d, --dist : Use which metric of distance? Options:
Individual-based:
PDIST : Uncorrected p-distances [# Differences / Length]
Frequency models (when using --pop):
FST : Weir and Cockerham's Fst formulation (=THETAst)
LINFST : [default] Rousset's (1997) Fst [=Fst/(1-Fst)]
JOST : Jost's (2008) D
CHORD : Cavalli-Sforza and Edwards (1967) chord distance
--NOTE: Individual-based metrics can also be computed for
populations. You can set how these are aggregated w/ --pop_agg
--NOTE: Multiple loci for PDIST
will be reported using the method defined in --loc_agg
-G, --genmat : Skip calculation and use the provided labeled .tsv matrix
--coercemat : [Boolean] Coerce negative values in input matrix to zero
--het : [Boolean] Count partial differences [e.g. ind1=T, ind2=W]
--global_het : Estimate Ht using global frequencies (default is averaged over pops)
DBSCAN options (only when --clusterpop):
--min_samples : Minimum samples per cluster [default=1]
--epsilon : Maximum distance (in km) within a cluster [default=20]
Aggregation options:
-P, --pop_agg : Define aggregator function for certain genetic distances in pop samples
-L, --loc_agg : Define aggregator function for aggregating locus-wise distances
All of these can take the following options:
ARITH : [default] Use arithmetic mean
MEDIAN : Use median distance
HARM : Use harmonic mean
ADJHARM : Adjusted harmonic mean (see docs)
GEOM : Use geometric mean
MIN : Use minimum distance
MAX : Use maximum distance
IBD options:
--perm : Number of permutations for mantel test [def=1000]
--and_log : Also perform IBD steps with log geographic distances
StreamTree options (see Kalinowski et al. 2008) :
-w, --weight : Desired weighting for least-squares fitting:
Options:
FM67 : Fitch and Margoliash (1967) [w = 1/D^2]
BEYER74 : Beyer et al. (1974) weights [w = 1/D]
CSE67 : [default] Cavalli-Sforza & Edwards (1967) [w = 1]
The main workflow control argument is -r/--run, which tells which steps of the pipeline you want to run. The options for this are:
- -r GENDIST: Only calculates a pairwise genetic distance matric for input samples
- -r STREAMDIST: Only calculates a pairwise matrix of hydrologic (stream) distances
- -r DISTANCES: Computes both of the above
- -r IBD: Computes both distance matrices and performes a simple Mantel test for isolation-by-distance
- -r STREAMTREE: Computes distance matrices and fits the StreamTree model
- -r ALL: All of the above
- -r RUNLOCI: All of the above, but fitting StreamTree models to each individual locus
Some of these are included only for convenience -- for example, there are much more comprehensive packages out there for computing genetic distance matrices, and I don't recommend the Mantel test as the sole means of testing for isolation-by-distance -- and in most cases I think -r ALL or -r STREAMTREE will be what you want.
Many of the runtime options relate to specific components of the required inputs, which I will discuss below.
Depending on the workflow you are running, some of these files may not be required (for example, computing genetic distances only will not require an input geodatabase).
The intended input format for the genotype data is the widely used VCF format. Some examples are provided in the example data/ directory, which were produced by the program ipyrad:
##fileformat=VCFv4.0
##fileDate=2021/03/21
##source=ipyrad_v.0.9.68
##reference=pseudo-reference (most common base at site)
##phasing=unphased
##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
##FORMAT=<ID=CATG,Number=1,Type=String,Description="Base Counts (CATG)">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT 63burk03 63cburk01 >
RAD_0 28 loc0_pos27 G A 13 PASS . GT:DP:CATG 0/0:81:0,0,0,81 >
RAD_0 76 loc0_pos75 C T 13 PASS . GT:DP:CATG 0/0:81:81,0,0,0 >
...
...
Parsing is faster with compressed and indexed files (and will be more space efficient), so I recommend keeping these compressed with bgzip and indexed with tabix:
# compress
bgzip test_sub100.vcf
# index
tabix test_sub100.vcf.gz
This file should be provided using -v/--vcf.
Individual metadata will be needed in the form of coordinates, which can be passed as a simple tab-delimited text file with header (see example in data/test.coords):
sample lat long
63burk03 26.925414 90.396139
63cburk01 26.92383 90.39815
63cburk02 26.92383 90.39815
63cdikc01 27.2676 90.04778
63cdikc02 27.2676 90.04778
63cdikc03 27.2676 90.04778
63cdolk01 26.88353 90.34272
63cdolk03 26.88353 90.34272
63cdort03 26.86776 89.37437
...
...
For population-level analysis, there are currently three ways in which you can define populations for population-wise analysis. One option (-g/--geopop) will group any samples into populations which "snap" to the same stream node (see below).
A third option (-c,--clusterpop) will automatically cluster geographically similar individuals using the DBSCAN algorithm in scikit-learn, using great-circle geographic distances (i.e., this is not informed by stream distances calculated as a part of some workflows). Two relevant options are provided for manipulating the DBSCAN results:
--min_samples : Minimum samples per cluster [default=1]
--epsilon : Maximum distance (in km) within a cluster [default=20]
or using an input file providing population assignments for each individual, again as a simple tab-delimited text file (see example data/test.popmap), passed via -p/--pops:
63burk03 burk
63cburk01 burk
63cburk02 burk
63dakp01 dakp
63dakp02 dakp
63dakp03 dakp
63dakp04 dakp
63dakp05 dakp
...
...
The input stream network can be provided as a shapefile, geodatabase, or GPKG file, all passed uing the -s/--shp option. There are a number of requirements for this file in order for the result to create a valid network. I highly recommend using the existing global stream datasets provided by the HydroLab group at McGill University, specifically the HydroAtlas or free-flowing rivers dataset as these are already properly formatted for use, and the additional variables included will make downstream analysis very easy.
If for some reason you cannot use the HydroRIVERS dataset, you will need to do some things first before loading your shapefile into autoStreamTree. First, you will need to include two variables in the attribute table of your shapefile: 1) REACH_ID (case sensitive) must provide a unique identifier to each stream reach; and 2) LENGTH_KM should give the length of each segment. Next, because sometime large stream layers will have small gaps in between streams, you will need to span any small gaps between streams which should be contiguous, and also dissolve any lines that overlap with one another so that any given section of river is represented by a single line. I will provide a tutorial for doing this in ArcMAP later, but for now there are some scripts in our complementary package that can help with these steps using the ArcPy API: https://github.com/stevemussmann/StreamTree_arcpy. Note that this package will also help you in running the original Stream Tree package on Windows, if you want to do so.
Note that a valid path is required between all sites in order to calculate pairwise stream distances. Thus, if you are analyzing data from multiple drainages which only share an oceanic connection, you will need to augment the shapefile. For example this could be accomplished by adding a vector representing the coastline to create an artificial connection among drainages.
There are a number of existing (and more comprehensive) packages out there for computing pairwise genetic distance matrices. If you already have this (either at individual or population level), you can provide a labelled matrix as a tab-delimited text file with --genmat. An example of how this should be formatted may be found in data/test.popGenDistMat.txt.
For convenience, a number of options are built-in, which can be selected using the -d,--dist argument:
-d, --dist : Use which metric of distance? Options:
Individual-based:
PDIST : Uncorrected p-distances [# Differences / Length]
Frequency models (when using --pop):
FST : Weir and Cockerham's Fst formulation (=THETAst)
LINFST : [default] Rousset's (1997) Fst [=Fst/(1-Fst)]
JOST : Jost's (2008) D
CHORD : Cavalli-Sforza and Edwards (1967) chord distance
--NOTE: Individual-based metrics can also be computed for
populations. You can set how these are aggregated w/ --pop_agg
--NOTE: Multiple loci for PDIST, and JC69 distances
will be reported using the method defined in --loc_agg
For most use cases, I would suggest -d LINFST which will compute a "linearised" version of Weir and Cockerham's Theta-ST.
Optionally, the user can also opt to aggregate individual-based distance measures, either those provided (p-distances) or from an input matrix that is only at the individual level. This can be provided using the --pop_agg argument, with any of the following options available:
Aggregation options:
-P, --pop_agg : Define aggregator function for certain genetic distances in pop samples
-L, --loc_agg : Define aggregator function for aggregating locus-wise distances
All of these can take the following options:
ARITH : [default] Use arithmetic mean
MEDIAN : Use median distance
HARM : Use harmonic mean
ADJHARM : Adjusted harmonic mean (see docs)
GEOM : Use geometric mean
MIN : Use minimum distance
MAX : Use maximum distance
Another useful feature is the ability to concatenate the input variant data -- this can be done either globally (for example if you want to only compute a global p-distance) with -C all, or if you have phased data used to form "pseudo" microhaplotypes using -C loc, which will group variants using the CHROM field in the input VCF. Note that if using a program such as ipyrad (e.g., for RADseq data), the entries in this field will represent 'independent' loci -- if you have data aligned to a genome and want to define loci in some way you will need to insert this information into the CHROM field as a pre-processing step.
If running the full workflow, the first thing autoStreamTree will do upon reading your input geodatabase is to calculate a minimally reduced sub-network which collapses the input river network into continuous reaches (="edges"), with nodes either representing sample localities or junctions. Because the full river network will likely contain many branches and contiguous reaches which do not contain samples, these are removed to speed up computation. The underlying metadata will be preserved, and the final output will consist of an annotated shapefile containing an EDGE_ID attribute which tells you how reaches were dissolved into contiguous edges in the graph, and a FittedD attribute giving the least-squares optimized distances.
The reduced sub-network will be plotted for you in a file called out.subGraph.pdf.
Here, the total cumulative stream length (in km) is plotted along edges (NOTE: Any natural curvature in the river is not preserved in this plot), with sample sites as blue dots and junctions as black dots. A geographically accurate representation, coloring individual streams to designate different dissolved edges, will be provided as out.streamsByEdgeID.pdf.
After fitting genetic distances, autoStreamTree will create several other outputs. First, a table called out.reachToEdgeTable.txt will give a tab-delimited map of how REACH_ID attributes were dissolved into contiguous edges. Second, a tabular and graphical representation of how fitted pairwise distances compare to the raw calculates (or user-provided) pairwise distances: out.obsVersusFittedD.txt and out.obsVersusFittedD.pdf
Finally, the fitted distances per stream edge will be output both as an added column to the original shapefile attribute table (out.streamTree.shp and out.streamTree.txt), and also as a plot showing how distances compare across all streams.
If you have just installed autoStreamTree and are running it for the first time, I recommend you first run the example analysis using the provided files in the autostreamtree/data directory. These include all necessary inputs, and a geodatabase. To run the full workflow on the example data, simply use:
# Change directories to the autoStreamTree repository
cd autostreamtree
# run the analysis
autostreamtree -s autostreamtree/data/test.shp -i autostreamtree/data/test.coords -v autostreamtree/data/test_sub100.vcf.gz -p autostreamtree/data/test.popmap -r ALL --reachid_col "HYRIV_ID" --length_col "LENGTH_KM" -o test
This will produce a number of output text files and plots using the prefix provided with -o.
autoStreamTree is designed to aid in the downstream analysis of genetic differentiation, adaptation, and ecological aspects of aquatic species, although it is versatile enough to be applicable to any dataset structured as a network.
A key use case involves the examination of locus-wise genetic distances across network segments. This is efficiently done by importing the geodatabase output of autoStreamTree using the -r LOC option into R or a similar analytical platform. An example of analysing variation among fitted locus-wise distances as a function of environmental variables included in the HydroATLAS dataset is provided as a NextFlow pipeline, using forward-selection to reduce features and redundancy analysis (RDA) implemented in ecopy, can be found here.
autoStreamTree is currently distributed with two utility scripts: networkDimensions.py and streeToDendrogram.py. We expect this list to grow, and if you need help writing any specific utilities using autoStreamTree outputs, please don't hesitate to get in touch!
As with the autoStreamTree CLI, when installed via pip or conda/mamba, these can be accessed via front-ends networkDimensions and streeToDendrogram, both having help menus displayed by calling with -h
networkDimensions is a simple script to capture the spatial dimensions of your minimized network, including the total length, and the area of a the minimally bounding convex hull.
The options are:
(autostreamtree) tyler@Tylers-MacBook-Pro-2 autostreamtree % networkDimensions -h
usage: networkDimensions [-h] network_file
Calculate total lineage length and bounding box area of a network.
positional arguments:
network_file Path to the pickled Networkx graph file.
options:
-h, --help show this help message and exit
Simply provide the output .network file created by autoStreamTree.
streeToDendrogram makes it easier to visualise the fitted distances as a dendrogram (rather than a colored spatial network). The options are:
(autostreamtree) tyler@Tylers-MacBook-Pro-2 autostreamtree % streeToDendrogram -h
usage: streeToDendrogram [-h] --shp SHP --points POINTS [--pop POP] [--edge_id EDGE_ID]
[--dist DIST] [--out OUT]
Plot a stream tree with fittedD attribute as dendrogram
options:
-h, --help show this help message and exit
--shp SHP Network as shapefile
--points POINTS Sample coordinates
--pop POP Population map file (optional)
--edge_id EDGE_ID Edge ID attribute.
--dist DIST Dist attribute.
--out OUT Output prefix
All utilities from autoStreamTree are intended to be easy to run within an automated pipeline. An example of building these into a SnakeMake workflow can be found in the Open Science Framework repository (doi: 10.17605/OSF.IO/4UXFJ).
For example, in the run_spd.smk file, you will find an example of fitting distances for regional subsets of samples for an empirical ddRADseq dataset, and then performing downstream environmental resistance modelling on each using ResistNet
Below is a full list of citations for the various methods used. Apologies to anyone I missed - please let me know if you notice any discrepancies.
- Beyer WM, Stein M, Smith T, Ulam S. 1974. A molecular sequence metric and evolutionary trees. Mathematical Biosciences. 19: 9-25.
- Cavalli-Sforza LL, Edwards AWF. 1967. Phylogenetic analysis: model and estimation procedures. American Journal of Human Genetics. 19: 233-257.
- Ester M, Kriegel HP, Sander J, Xu X. 1996. A density-based algorithm for discovering clusters in large spatial databases with noise. IN: Simoudis E, Han J, Fayyad UM. (eds.). Proceedings of the Second International Conference on Knowledge Discovery and Data Mining (KDD-96). AAAI Press. pp. 226–231.
- Felsenstein J. 2004. Inferring Phylogenies: Chapter 11. Sunderland: Sinauer.
- Fitch WM, Margloiash E. 1967. Construction of phylogenetic trees. Science. 155: 279-84.
- Hagberg A, Swart P, S Chult D. 2008. Exploring network structure, dynamics, and function using NetworkX. Los Alamos National Lab.(LANL), Los Alamos, NM
- Hedrick PW. 2005. A standardized genetic differentiation measure. Evolution. 59: 1633–1638
- Jordahl K. 2014. GeoPandas: Python tools for geographic data. URL: https://github.com/geopandas/geopandas.
- Jost L. 2008. Gst and its relatives do not measure differentiation. Molecular Ecology. 17: 4015-4026.
- Kalinowski ST, MH Meeuwig, SR Narum, ML Taper (2008) Stream trees: a statistical method for mapping genetic differences between populations of freshwater organisms to the sections of streams that connect them. Canadian Journal of Fisheries and Aquatic Sciences (65:2752-2760)
- Kimura M. 1980. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution. 16(2): 111-120.
- Mantel N. 1967. The detection of disease clustering and a generalized regression approach. Cancer Research 27(2): 209-220.
- Meirmans PG, Hedrick PW. 2011. Assessing population structure: Fst and related measures. Molecular Ecology Resources. 11: 5-18.
- Nei M. 1972. Genetic distance between populations. American Naturalist. 106: 283-292.
- Nei M. 1987. Molecular Evolutionary Genetics. Columbia University Press, New York
- Nei M, Chesser RK. 1983. Estimation of fixation indices and gene diversities. Annals of Human Genetics 47(3): 253-259.
- Pedregosa F, Varoquaux G, Gramfort A, Michel V, Thirion B, Grisel O, Blondel M, Prettenhofer P, Weiss R, Dubourg V, Vanderplas J. 2011. Scikit-learn: Machine learning in Python. The Journal of machine Learning research. 1(12):2825-30
- Rossmann LA. DFLOW User's Manual. U.S. Environmental Protection Agency.[For description of zero-adjusted harmonic mean]
- Rousset F. 1997. Genetic differentiation and estimation of gene flow from F-statistics under isolation by distance. Genetics. 145: 1219-28.
- Tajima F, Nei M. 1984. Estimation of evolutionary distance between nucleotide sequences. Molecular Biology and Evolution 1:269-285
- Tamura K, Nei M. 1993. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution. 10(3):512-526.
- Weir BS, Cockerham CC. 1984. Estimating F-statistics for the analysis of population structure. Evolution. 38: 1358-1370.
Here are some recommended readings and resources:
- Comte L, Olden JD. 2018. Fish dispersal in flowing waters: A synthesis of movement- and genetic-based studies. Fish and Fisheries. 19(6): 1063-1077.
- Comte L, Olden JD. 2018. Evidence for dispersal syndromes in freshwater fishes. Proceedings Royal Society: B. 285(1871):
- Grill, G., Lehner, B., Thieme, M. et al. 2019. Mapping the world’s free-flowing rivers. Nature. 569:215–221.
- Linke S, Lehner B, Ouellet Dallaire C. et al. 2019. Global hydro-environmental sub-basin and river reach characteristics at high spatial resolution. Sci Data 6, 283
- Meffe GK, Vrijenhoek RC. 1988. Conservation genetics in the management of desert fishes. Conservation Biology. 2(2):157-69.
- Meirmans PG. 2012. The trouble with isolation by distance. Molecular Ecology 21(12): 2839-46.
- Sere M, Thevenon S, Belem AMG, De Meeus T. 2017. Comparison of different genetic distances to test isolation by distance between populations. 2017. 119(2):55-63.
- Thomaz AT, Christie MR, Knowles LL. 2016. The architecture of river networks can drive the evolutionary dynamics of aquatic populations. Evolution. 70(3): 731-739.
- Tonkin JD, Altermatt F, Finn DS, Heino J, Olden JD, Pauls SU, Lytle DA. 2017. The role of dispersal in river network metacommunities: Patterns, processes, and pathways. Freshwater Biology. 61(1): 141-163.
- Wright S. 1965. Isolation by distance. Genetics. 28: 114-138.
If you are interested in contributing to autoStreamTree, first of all thank you! Any form of contribution is always welcome, be that bug reports, code review, bug fixes, or even adding new features! For reference, API documentation can be found at https://tkchafin.github.io/autostreamtree/, which will be re-built upon each update to the repository.
If you encounter a problem in using or installing autoStreamTree, please post to the GitHub Issues page. If you do so, please be sure to share the full steps which led to your problem, and the full output (including any error messages). In some instances it may be necessary to see your input files.
If you would like to contribute any changes to the code, just follow these steps!
- Fork the repository
- Make changes
- Submit a pull request
That's it! If you have an idea for a feature that would be helpful for your research, but aren't sure how to implement it, this can be logged using the GitHub Issues page linked above and I'll do my best to help!