gencodegenes


Namegencodegenes JSON
Version 1.1.4 PyPI version JSON
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home_pagehttps://github.com/jeremymcrae/gencodegenes
SummaryPackage to load genes from GENCODE GTF files
upload_time2024-09-20 20:09:30
maintainerNone
docs_urlNone
authorJeremy McRae
requires_python>=3.8
licenseMIT
keywords
VCS
bugtrack_url
requirements No requirements were recorded.
Travis-CI No Travis.
coveralls test coverage No coveralls.
            
### GENCODEGenes

This package loads genes from GENCODE GTF/GFF files, groups transcripts by gene, 
and provides methods for transcripts, so you can find exon coordinates, CDS 
distances and sequences.

### Install
```sh
pip install gencodegenes
```

### Usage

```py
from gencodegenes import Gencode

gencode = Gencode(GTF_PATH)
# full function arguments are Gencode(gtf_path, fasta_path=None, coding_only=True)
#  - fasta_path: pass in path to fasta file to get gene transcripts with sequence
#  - coding_only: pass in False to include all transcripts, not just protein coding

# get gene by HGNC symbol
gene = gencode['OR5A1']
transcripts = gene.transcripts
canonical = gene.canonical  # picks MANE transcript if available, if none named
                            # as MANE, picks the one tagged as appris_principal
                            # (or longest CDS if multiple), if none tagged, picks
                            # the longest protein coding, if none protein coding,
                            # picks the longest cDNA 
gene.start, gene.end, gene.chrom, gene.strand, gene.symbol # other attributes available


# find gene nearest a genomic position, or overlapping a genomic region
gencode.nearest('chr1', 1000000)
gencode.in_region('chr1', 1000000, 2000000)

# and the transcript has a bunch of methods
tx = gene.canonical
tx.in_exons(pos)                         # check if pos in exons
tx.in_coding_region(pos)                 # check if pos in CDS
tx.get_coding_distance(pos)              # get distance in CDS to CDS start
tx.get_closest_exon(pos)                 # find exon closest to position
tx.get_position_on_chrom(cds_pos)        # convert CDS pos to genomic pos
tx.get_codon_info(pos)                   # get info about codon for a site
tx.get_codon_number_for_cds_pos(cds_pos) # convert CDS pos to codon number
tx.translate(seq)                        # translate DNA to AA (if opened with Fasta)

# the transcript also has associated data fields
tx.name         # transcript ID
tx.chrom        # transcript chromosome
tx.start        # transcript start (TSS)
tx.end          # transcript end
tx.cds_start    # CDS start position
tx.cds_end      # CDS end position 
tx.type         # transcript type e.g. protein_coding
tx.strand       # strand (+ or -)
tx.exons        # list of exon coordinates
tx.cds          # list of CDS coordinates
tx.cds_sequence # get cDNA sequence (if Gencode was opened with fasta)

```

            

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    "description": "\n### GENCODEGenes\n\nThis package loads genes from GENCODE GTF/GFF files, groups transcripts by gene, \nand provides methods for transcripts, so you can find exon coordinates, CDS \ndistances and sequences.\n\n### Install\n```sh\npip install gencodegenes\n```\n\n### Usage\n\n```py\nfrom gencodegenes import Gencode\n\ngencode = Gencode(GTF_PATH)\n# full function arguments are Gencode(gtf_path, fasta_path=None, coding_only=True)\n#  - fasta_path: pass in path to fasta file to get gene transcripts with sequence\n#  - coding_only: pass in False to include all transcripts, not just protein coding\n\n# get gene by HGNC symbol\ngene = gencode['OR5A1']\ntranscripts = gene.transcripts\ncanonical = gene.canonical  # picks MANE transcript if available, if none named\n                            # as MANE, picks the one tagged as appris_principal\n                            # (or longest CDS if multiple), if none tagged, picks\n                            # the longest protein coding, if none protein coding,\n                            # picks the longest cDNA \ngene.start, gene.end, gene.chrom, gene.strand, gene.symbol # other attributes available\n\n\n# find gene nearest a genomic position, or overlapping a genomic region\ngencode.nearest('chr1', 1000000)\ngencode.in_region('chr1', 1000000, 2000000)\n\n# and the transcript has a bunch of methods\ntx = gene.canonical\ntx.in_exons(pos)                         # check if pos in exons\ntx.in_coding_region(pos)                 # check if pos in CDS\ntx.get_coding_distance(pos)              # get distance in CDS to CDS start\ntx.get_closest_exon(pos)                 # find exon closest to position\ntx.get_position_on_chrom(cds_pos)        # convert CDS pos to genomic pos\ntx.get_codon_info(pos)                   # get info about codon for a site\ntx.get_codon_number_for_cds_pos(cds_pos) # convert CDS pos to codon number\ntx.translate(seq)                        # translate DNA to AA (if opened with Fasta)\n\n# the transcript also has associated data fields\ntx.name         # transcript ID\ntx.chrom        # transcript chromosome\ntx.start        # transcript start (TSS)\ntx.end          # transcript end\ntx.cds_start    # CDS start position\ntx.cds_end      # CDS end position \ntx.type         # transcript type e.g. protein_coding\ntx.strand       # strand (+ or -)\ntx.exons        # list of exon coordinates\ntx.cds          # list of CDS coordinates\ntx.cds_sequence # get cDNA sequence (if Gencode was opened with fasta)\n\n```\n",
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