the Python Gene Order Plotter
Project description
geneorder
This package was born out of my continuous efforts to write streamlined
code to plot Hox gene clusters. It seems like this is a task I will be
performing many times, and there don’t seem to be too many tools out
there, so I wrote my own. This is my matplotlib-based answer, and I
hope that it is useful to you, too.
Input
Generally, the package expects you to have, at least, knowledge of the gene IDs that you want to visualize, and knowledge of their coordinates in the genome. This can be manually encoded or come in table form - crucially, it can be read from a GFF3 file.
Usage
Installation
Install latest from the GitHub repository:
$ pip install git+https://github.com/galicae/geneorder.git
or from pypi
$ pip install geneorder
Documentation
Documentation can be found hosted on this GitHub repository’s pages. Additionally you can find package manager specific guidelines on pypi.
How to use
The most basic geneorder use case is when you have a list of genes
that are co-linear and would like to plot them in their chromosomal
context. The least information that is needed for that is
- the chromosome name
- the gene IDs/names
- the starts/ends of all genes
- the strand and orientation of the genes
import pandas as pd
from geneorder.core import plot_synteny_schematic
gene_dict = {
"gene_name": [
"Hox1",
"Hox2",
"Hox3",
"Hox4",
"Hox5",
"Hox6",
"Hox7",
"Hox8",
"Hox10",
],
"gene_id": [
"PB.8615",
"g9718",
"PB.8616",
"g9720",
"g9721",
"PB.8617",
"g9723",
"g9724",
"g9725",
],
"start": [
1927066,
1998922,
2058396,
2195412,
2351936,
2373415,
2565196,
2916314,
2986021,
],
"end": [
1936157,
2024148,
2065953,
2206712,
2354374,
2375678,
2594468,
2926445,
2996225,
],
}
minimal = pd.DataFrame(gene_dict)
minimal["seqid"] = "pseudochrom_56"
minimal["strand"] = "-"
minimal
| gene_name | gene_id | start | end | seqid | strand | |
|---|---|---|---|---|---|---|
| 0 | Hox1 | PB.8615 | 1927066 | 1936157 | pseudochrom_56 | - |
| 1 | Hox2 | g9718 | 1998922 | 2024148 | pseudochrom_56 | - |
| 2 | Hox3 | PB.8616 | 2058396 | 2065953 | pseudochrom_56 | - |
| 3 | Hox4 | g9720 | 2195412 | 2206712 | pseudochrom_56 | - |
| 4 | Hox5 | g9721 | 2351936 | 2354374 | pseudochrom_56 | - |
| 5 | Hox6 | PB.8617 | 2373415 | 2375678 | pseudochrom_56 | - |
| 6 | Hox7 | g9723 | 2565196 | 2594468 | pseudochrom_56 | - |
| 7 | Hox8 | g9724 | 2916314 | 2926445 | pseudochrom_56 | - |
| 8 | Hox10 | g9725 | 2986021 | 2996225 | pseudochrom_56 | - |
plot_synteny_schematic(minimal)
The plot can be customized, e.g. by including color:
minimal["color"] = [
"red",
"orange",
"gold",
"lightgreen",
"forestgreen",
"royalblue",
"darkblue",
"darkmagenta",
"magenta",
]
plot_synteny_schematic(minimal)
We can also edit the dataframe to indicate missing genes:
from geneorder import util
minimal = util.insert_gap(
minimal,
"Hox8",
"Hox10",
"gene_name",
no_gaps=1,
purge_columns=["gene_id", "color"],
)
plot_synteny_schematic(minimal)
For more details, please refer to the documentation.
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