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GenomicRanges

Python equivalent to Bioconductor's GenomicRanges to represent genomic locations and support genomic analysis. It uses efficient structures already available in the Python/Pandas/numpy eco-system adds an familiar interfaces.

Install

Package is deployed to PyPI

pip install genomicranges

Usage

The package provide several ways to represent genomic intervals

Pandas DataFrame

A common representation in Python is a pandas DataFrame for all tabular datasets. One can convert this into GenomicRanges.

Note: The DataFrame must contain columns seqname, start and end that represent chromosome and genomic coordinates.

from genomicranges import GenomicRanges

gr = GenomicRanges.fromPandas(<PANDAS DATA FRAME>)

From UCSC or GTF file

Methods are available to easily access UCSC genomes or load a genome annotation from GTF

from genomicranges import GenomicRanges

gr = GenomicRanges.fromGTF(<PATH TO GTF>)
# OR 
gr = GenomicRanges.fromUCSC(genome="hg19")

Interval Operations

Currently supports Nearest Genomic positions operation in Bioconductor, but more coming soon.

subject = GenomicRanges.fromUCSC(genome="hg38")

query = GenomicRanges.fromPandas(
    pd.DataFrame(
        {
            "seqname": ["chr1", "chr2", "chr3"],
            "start": [100, 115, 119],
            "end": [103, 116, 120],
        }
    )
)

hits = subject.nearest(query)
print(hits)

Note

This project has been set up using PyScaffold 4.1.1. For details and usage information on PyScaffold see https://pyscaffold.org/.

Release files for genomicranges 0.1

For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.

Source distribution (sdist)

Source distribution for genomicranges 0.1
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Built distribution (wheel)

Table of built distributions (wheels) for genomicranges 0.1
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GenomicRanges-0.1-py3-none-any.whl Python 3 none any Details

Total release size: 30.7 kB

Release files / GenomicRanges-0.1.tar.gz

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