Biopython - sequences and alphabets

The Sequence object

Some examples will also require a working internet connection in order to run.

>>> from Bio.Seq import Seq
>>> from Bio.Alphabet import IUPAC >>> my_seq = Seq("AGTACACTGGT", IUPAC.unambiguous_dna) >>> my_seq Seq('AGTACACTGGT', IUPACUnambiguousDNA()) >>> my_seq.alphabet IUPACUnambiguousDNA() 

A Seq object in python acts like a normal python string.

>>> for letter in my_seq: ... print letter >>> len(my_seq) >>> my_seq[4:12] >>> my_seq[::-1] >>> str(my_seq) 

Nucleotide counts, transcription, translation

>>> my_seq.count("A") 3 

to get the GC nucleotide content.

>>> from Bio.SeqUtils import GC
>>> GC(my_seq) 45.45454545454545 

transcription and translation

>>> my_mRNA = my_seq.transcribe() Seq('AGUACACUGGU', IUPACUnambiguousRNA()) >>> my_seq.translate() Seq('STL', IUPACProtein()) 

complement and reverse complement

>>> str(my_seq)
'AGTACACTGGT' >>> my_seq.complement() Seq('TCATGTGACCA', IUPACUnambiguousDNA()) >>> my_seq.reverse_complement() Seq('ACCAGTGTACT', IUPACUnambiguousDNA()) 

You can translate directly from the DNA coding sequence or you can use the mRNA directly.

>>> from Bio.Seq import Seq
>>> from Bio.Alphabet import IUPAC >>> messenger_rna = Seq("AUGGCCAUUGUAAUGGGCCGCUGAAAGGGUGCCCGAUAG", IUPAC.unambiguous_rna) >>> messenger_rna Seq('AUGGCCAUUGUAAUGGGCCGCUGAAAGGGUGCCCGAUAG', IUPACUnambiguousRNA()) >>> messenger_rna.translate() Seq('MAIVMGR*KGAR*', HasStopCodon(IUPACProtein(), '*')) 

Now, you may want to translate the nucleotides up to the first in frame stop codon, and then stop (as happens in nature):

>>> coding_dna.translate()
Seq('MAIVMGR*KGAR*', HasStopCodon(IUPACProtein(), '*')) >>> coding_dna.translate(to_stop=True) Seq('MAIVMGR', IUPACProtein()) 

Exercise

1. There is so much stuff available in biopython.  What happens if you do this?

   >>> from Bio.Data import CodonTable
   >>> standard_table = CodonTable.unambiguous_dna_by_id[1] >>> mito_table = CodonTable.unambiguous_dna_by_id[2] >>> print standard_table >>> print mito_table 

The Sequence record object

The SeqRecord objects are the basic data type for the SeqIO objects and they are very similar to Seq objects,however, there are a few additional attributes.

• seq  - The sequence itself, typically a Seq object.
• id    - The primary ID used to identify the sequence – a string. In most cases this is something like an accession number.
• name - A ‘common’ name/id for the sequence – a string. In some cases this will be the same as the accession number, but it could also be a clone name. Analagous to the LOCUS id in a GenBank record.
• description - A human readable description or expressive name for the sequence – a string.

We can think of the SeqRecord as a container that has the above attributes including the Seq.

Exercise

1. Copy the following script into an editor and save as ‘BioSequences.py’
2. Open a terminal window and cd into the appropriate directory.
3. Fill in the missing lines with code

from Bio.Seq import Seq
from Bio.SeqRecord import SeqRecord ## create a simple SeqRecord object simple_seq = Seq("GATCAGGATTAGGCC") simple_seq_r = SeqRecord(simple_seq) simple_seq_r.id = "AC12345" simple_seq_r.description = "I am not a real sequence" ## print summary print simple_seq_r.id print simple_seq_r.description print str(simple_seq_r.seq) print simple_seq_r.seq.alphabet ## translate the sequence translated_seq = simple_seq_r.seq.translate() print translated_seq # exercise 1 -- translate the sequence only until the stop codon # exercise 2 -- get the reverse complement of the sequence # exercise 3 -- get the reverse of the sequence (just like for lists) # exercise 4 -- get the GC nucleotide content 

The Sequence IO object

There is one more object that we have to discuss and this the SeqIO object is like a container for multiple SeqRecord objects.

import os
from Bio import SeqIO ''' We use a list here to save the gene records from a FASTA file If you have many records a dictionary will make the program faster. ''' ## save the sequence records to a list allSeqRecords = [] allSeqIDs = [] pathToFile = os.path.join("..","data","ls_orchid.fasta") for seq_record in SeqIO.parse(pathToFile, "fasta"): allSeqRecords.append(seq_record) allSeqIDs.append(seq_record.id.split("|")[1]) print seq_record.id print str(seq_record.seq) print len(seq_record) ## print out fun stuff about the sequences print "We found ", len(allSeqIDs), "sequences" print "information on the third sequence:" ind = 2 seqRec = allSeqRecords[ind] print "\t", "GI number ", allSeqIDs[ind] print "\t", "full id ", seqRec.id print "\t", "num nucleo. ", len(seqRec.seq) print "\t", "1st 10 nucleo.", seqRec.seq[:10] 

Just as easy as it is to read a set of files we can save modified versions (i.e. QA). Also, it is almost the exact same code as above to parse sequences from a GenBank (.gb) file.

There is really way to much to cover in the time we have, but if you have Next Generation Sequencing data then refer to sections 4.8, 16.1.7 and 16.1.8 of the biopython tutorial. There is even support for binary formats (i.e. SFF).

转载于:https://www.cnblogs.com/pennyy/p/4119577.html