LucaCappelletti94/ucsc_genomes_downloader

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Metadata-Version: 2.1
Name: ucsc-genomes-downloader
Version: 1.1.26
Summary: Python package to quickly download genomes from the UCSC.
Home-page: https://github.com/LucaCappelletti94/ucsc_genomes_downloader
Author: Luca Cappelletti
Author-email: cappelletti.luca94@gmail.com
License: MIT
Description: UCSC Genomes Downloader
        =========================================================================================
        |python_version| |pip| |downloads|
        
        Python package to quickly download and process genomes from the UCSC website.
        
        How do I install this package?
        ----------------------------------------------
        As usual, just download it using pip:
        
        .. code:: shell
        
            pip install ucsc_genomes_downloader
            
        Getting COVID-19 Genome
        ----------------------------------------------
        To download the COVID19 genome just run:
        
        .. code:: python
        
            from ucsc_genomes_downloader import Genome
            covid = Genome("wuhCor1")
            
            genome = covid["NC_045512v2"]
        
        
        Usage examples
        --------------
        
        Simply instantiate a new genome
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        To download and load into memory the chromosomes of a given genomic assembly
        you can use the following code snippet:
        
        .. code:: python
        
            from ucsc_genomes_downloader import Genome
            hg19 = Genome(assembly="hg19")
        
        Downloading selected chromosomes
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        If you want to select a subset of chromosomes to be downloaded
        you can use the attribute "chromosomes":
        
        .. code:: python
        
            from ucsc_genomes_downloader import Genome
            hg19 = Genome("hg19", chromosomes=["chr1", "chr2"])
        
        Getting gaps regions
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        The method returns a DataFrame in bed-like format
        that contains the regions where only n or N nucleotides
        are present.
        
        .. code:: python
        
            all_gaps = hg19.gaps() # Returns gaps (region formed of Ns) for all chromosomes
            # Returns gaps for chromosome chrM
            chrM_gaps = hg19.gaps(chromosomes=["chrM"])
        
        Getting filled regions
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        The method returns a DataFrame in bed-like format
        that contains the regions where no unknown nucleotides
        are present, basically the complementary
        of the gaps method.
        
        .. code:: python
        
            all_filled = hg19.filled() # Returns filled for all chromosomes
            # Returns filled for chromosome chrM
            chrM_filled = hg19.filled(chromosomes=["chrM"])
        
        Removing genome's cache
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        To delete the cache of the genome, including chromosomes
        and metadata you can use the delete method:
        
        .. code:: python
        
            hg19.delete()
        
        Genome objects representation
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        When printed, a Genome object has a human-readable representation.
        This allows you to print lists of Genome objects as follows:
        
        .. code:: python
        
            print([
                hg19,
                hg38,
                mm10
            ])
        
            # >>> [
            #    Human, Homo sapiens, hg19, 2009-02-28, 25 chromosomes,
            #    Human, Homo sapiens, hg38, 2013-12-29, 25 chromosomes,
            #    Mouse, Mus musculus, mm10, 2011-12-29, 22 chromosomes
            # ]
        
        Obtaining a given bed file sequences
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        Given a pandas DataFrame in bed-like format, you can obtain
        the corresponding genomic sequences for the loaded assembly
        using the bed_to_sequence method:
        
        .. code:: python
        
            my_bed = pd.read_csv("path/to/my/file.bed", sep="\t")
            sequences = hg19.bed_to_sequence(my_bed)
        
        Properties
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        A Genome object has the following properties:
        
        .. code:: python
        
            hg19.assembly # Returns "hg19"
            hg19.date # Returns "2009-02-28" as datetime object
            hg19.organism # Returns "Human"
            hg19.scientific_name # Returns "Homo sapiens"
            hg19.description # Returns the brief description as provided from UCSC
            hg19.path # Returns path where genome is cached
        
        
        Utilities
        -------------------------------
        
        Retrieving a list of the available genomes
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        You can get a complete list of the genomes available
        from the UCSC website with the following method:
        
        .. code:: python
        
            from ucsc_genomes_downloader.utils import get_available_genomes
            all_genomes = get_available_genomes()
        
        
        Tessellating bed files
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        Create a tessellation of a given size of a given bed-like pandas dataframe.
        
        Available alignments are to the left, right or center.
        
        .. code:: python
        
            from ucsc_genomes_downloader.utils import tessellate_bed
            import pandas as pd
        
            my_bed = pd.read_csv("path/to/my/file.bed", sep="\t")
            tessellated = tessellate_bed(
                my_bed,
                window_size=200,
                alignment="left"
            )
        
        Expand bed files regions
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        Expand a given dataframe in bed-like format using selected alignment.
        
        Available alignments are to the left, right or center.
        
        .. code:: python
        
            from ucsc_genomes_downloader.utils import expand_bed_regions
            import pandas as pd
        
            my_bed = pd.read_csv("path/to/my/file.bed", sep="\t")
            expanded = expand_bed_regions(
                my_bed,
                window_size=1000,
                alignment="left"
            )
        
        Wiggle bed files regions
        ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
        Generate new bed regions based on a given bed file by wiggling the
        initial regions.
        
        .. code:: python
        
            from ucsc_genomes_downloader.utils import wiggle_bed_regions
            import pandas as pd
        
            my_bed = pd.read_csv("path/to/my/file.bed", sep="\t")
            expanded = wiggle_bed_regions(
                my_bed,
                max_wiggle_size=100, # Maximum amount to wiggle region
                wiggles=10, # Number of wiggled samples to introduce
                seed=42 # Random seed for reproducibility
            )
        
        .. _hg19: https://www.ncbi.nlm.nih.gov/assembly/GCF_000001405.13/
        
        .. |pip| image:: https://badge.fury.io/py/ucsc-genomes-downloader.svg
            :target: https://badge.fury.io/py/ucsc-genomes-downloader
            :alt: Pypi project
        
        .. |downloads| image:: https://pepy.tech/badge/ucsc-genomes-downloader
            :target: https://pepy.tech/badge/ucsc-genomes-downloader
            :alt: Pypi total project downloads
        
        .. |python_version| image:: https://img.shields.io/badge/python-3.x-blue
            :alt: Supported Python Versions
Platform: UNKNOWN
Classifier: Development Status :: 3 - Alpha
Classifier: License :: OSI Approved :: MIT License
Classifier: Programming Language :: Python :: 3
Requires-Python: >3.5.2
Provides-Extra: test