Implementation of GREAT in Python
Project description
greatpy
Implementation of GREAT in Python
Installation
You require Python 3.8 or newer installed on your system. In case you do not have
Python installed, we recommend installing Miniconda <https://docs.conda.io/en/latest/miniconda.html>
_.
Options to install greatpy
:
- Install the latest release of
greatpy
fromPyPI <https://pypi.org/project/greatpy/>
:
pip install greatpy
- Install the latest development version:
pip install git+https://github.com/theislab/greatpy.git@main
Notebooks
Information | link |
---|---|
Create regulatory domains file (regdom) | notebook |
Enrichment test (binomial/hypergeometric) | notebook |
Plotting of results | notebook |
Comparisons with GREAT | notebook |
Getting started
Please refer to
What is greatpy:
greatpy is a bioinformatics method that associates custom genomic regions to Gene Ontology (GO) terms by weighting genomic neighborhoods. It is based on and inspired by and inspired by GREAT (Genomic Regions Enrichment of Annotations Tool).
GREAT figure issue from GREAT article
Usage:
1. Create regulatory domain from tss
- Translate tab-separated files (
.tsv
or.bed
format) containing the following information:- Transcription start site annotations:
chromosome_number \t position \t strand \t gene_name
. - Chromosome sizes file should have the following columns :
chromosome_number \t chromosome_size
.
- Transcription start site annotations:
See data for input files
regdom = greatpy.tl.create_regdom(
tss_file=Input_TSS_path, # eg : "../data/human/hg38/tss.bed"
chr_sizes_file=Input_chromosome_size_path, # eg : "../data/human/hg38/chr_size.bed"
association_rule="Basalplusextention",
out_path=path_save_output,
)
Allowed association rules are:
Basalplusextention
OneCloset
TwoCloset
2. Get enrichment of GO term in the tests genomics regions
- This step calculates the significance of a custom set of genomic annotations through peak-gene mapping, using distal cis-regulatory regions of the genome.
- Input files :
- test file should have the following columns :
chr \t chr_start \t chr_end
. - regulatory domain file should have the following columns :
chr \t chr_start \t chr_end \t name \t tss strand
- chromosome size file should have the following columns :
chromosome_number \t chromosome_size
. - annotation file should have the following columns :
ensembl \t id \t name \t ontology.group \t gene.name \t symbol
See test cases for genomic input files.
res = greatpy.tl.enrichment(
test_file=Input_path_or_df, # eg : "../data/tests/test_data/input/10_MAX.bed"
regdom_file=regdom_path_or_df, # eg : "../data/human/hg38/regdom.bed"
chr_size_file=chromosome_size_path_or_df, # eg : "../data/human/hg38/chr_size.bed"
annotation_file=annotation_path_or_df, # eg : "../data/human/ontologies.csv"
)
Allowed tests for this function such as :
binom
(default True): it calculates the binomial p-value.hypergeom
(default True): it calculates the hypergeometric p-value.
Additionally, it is also possible to apply a Bonferroni and/or FDR correction to the found p-values:
res = great.tl.set_fdr(res, alpha=0.05)
res = great.tl.set_bonferroni(res, alpha=0.05)
3. Plot
1 Distribution of custom genomic annotations in regulatory domains
- Number of genetic associations per genomic region.
- Distance to the associated gene TSS for each genomic region studied.
- Absolute distance to the associated gene TSS for each genomic region studied.
fig, ax = plt.subplots(1, 3, figsize=(30, 8))
greatpy.pl.graph_nb_asso_per_peaks(
Input_path_or_df, # eg : "../data/tests/test_data/input/10_MAX.bed"
regdom_path_or_df, # eg : "../data/human/hg38/regdom.bed"
ax[0],
)
greatpy.pl.graph_dist_tss(
Input_path_or_df, # eg : "../data/tests/test_data/input/10_MAX.bed"
regdom_path_or_df, # eg : "../data/human/hg38/regdom.bed"
ax[0],
)
greatpy.pl.graph_absolute_dist_tss(
Input_path_or_df, # eg : "../data/tests/test_data/input/10_MAX.bed"
regdom_path_or_df, # eg : "../data/human/hg38/regdom.bed"
ax[0],
)
plt.show()
2 Enrichments by GO terms (dotplot) - one input
plot = enrichment_df.rename(columns={"binom_p_value": "p_value", "go_term": "name"})
plt.figure(figsize=(10, 10))
great.pl.plot_enrich(plot)
3 Enrichments by GO terms (dotplot) - multiple inputs
test = ["name_bindome_biosample_1", "name_bindome_biosample_2", "..."]
tmp_df = great.tl.enrichment_multiple(
tests=test,
regdom_file="../data/human/hg38/regulatory_domain.bed",
chr_size_file="../data/human/hg38/chr_size.bed",
annotation_file="../data/human/ontologies.csv",
binom=True,
hypergeom=True,
)
Notes
Both binomial and hypergeometric tests may be susceptible to biases of which one must be aware to analyze the results critically. The binomial test reduces the hypergeometric bias by taking into account exactly the size of the regulatory domains of the genes, whereas the hypergeometric test compensates for the bias of the binomial test by counting each gene only once. The two types of tests are complementary and are recommended to be analyzed together.
Release notes
See the changelog.
Contact
For questions and help requests, you can reach out in the scverse discourse. If you found a bug, please use the issue tracker.
Citation
If greatpy is useful for your research, please consider to cite as:
@software{greatpy,
author = {Ibarra, Mauger-Birocheau},
doi = {},
month = {},
title = {{greatpy}},
url = {https://github.com/theislab/greatpy},
year = {2022}
}
References
@article{GREAT,
author = {McLean, C.
and Bristor, D.
and Hiller, M. et al.},
title = {GREAT improves functional interpretation of cis-regulatory regions},
journal = {Nat Biotechnol},
year = {2010},
month = {May},
day = {02},
volume = {28},
number = {495},
pages = {501},
doi = {10.1038/nbt.1630},
url = {https://doi.org/10.1038/nbt.1630}
}
@Manual{rGREAT,
title = {rGREAT: GREAT Analysis - Functional Enrichment on Genomic Regions},
author = {Zuguang Gu},
year = {2022},
note = {https://github.com/jokergoo/rGREAT, http://great.stanford.edu/public/html/},
}
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