Is it possible in scikit-bio to extract genomic features stored in a gff3 formatted file from a genome fasta file?
Example:
genome.fasta
>sequence1
ATGGAGAGAGAGAGAGAGAGGGGGCAGCATACGCATCGACATACGACATACATCAGATACGACATACTACTACTATGA
annotation.gff3
#gff-version 3
sequence1 source gene 1 78 . + . ID=gene1
sequence1 source mRNA 1 78 . + . ID=transcript1;parent=gene1
sequence1 source CDS 1 6 . + 0 ID=CDS1;parent=transcript1
sequence1 source CDS 73 78 . + 0 ID=CDS2;parent=transcript1
The desired sequence for the mRNA feature (transcript1) would be the concatination of the two child CDS features. So in this case this would be 'ATGGAGCTATGA'
.
This feature has been added to scikit-bio, however the version available in bioconda does not support it yet (2017-12-15). The format file for gff3 is present in the Github repository.
You can clone the repo and install it locally using:
$ git clone https://github.com/biocore/scikit-bio.git
$ cd scikit-bio
$ python setup.py install
Following the example given in the file the following code should work:
import io
from skbio.metadata import IntervalMetadata
from skbio.io import read
gff = io.StringIO(open("annotations.gff3", "r").read())
im = read(gff, format='gff3', into=IntervalMetadata, seq_id="sequence1")
print(im)
For me this this raises a FormatIdentificationWarning
, but the entries are reported correctly:
4 interval features
-------------------
Interval(interval_metadata=<140154121000104>, bounds=[(0, 78)], fuzzy=[(False, False)], metadata={'source': 'source', 'type': 'gene', 'score': '.', 'strand': '+', 'ID': 'gene1'})
Interval(interval_metadata=<140154121000104>, bounds=[(0, 78)], fuzzy=[(False, False)], metadata={'source': 'source', 'type': 'mRNA', 'score': '.', 'strand': '+', 'ID': 'transcript1', 'parent': 'gene1'})
Interval(interval_metadata=<140154121000104>, bounds=[(0, 6)], fuzzy=[(False, False)], metadata={'source': 'source', 'type': 'CDS', 'score': '.', 'strand': '+', 'phase': 0, 'ID': 'CDS1', 'parent': 'transcript1'})
Interval(interval_metadata=<140154121000104>, bounds=[(72, 78)], fuzzy=[(False, False)], metadata={'source': 'source', 'type': 'CDS', 'score': '.', 'strand': '+', 'phase': 0, 'ID': 'CDS2', 'parent': 'transcript1'})
In the example in the code, the GFF3 and the FASTA file are concatenated in the input string used for the read function. Maybe that can fix this issue. Also I am not 100% sure how you can use the intervals returned to extract the feature.
If you love us? You can donate to us via Paypal or buy me a coffee so we can maintain and grow! Thank you!
Donate Us With