[Bioperl-l] Get variation included in genbank file
Chris Fields
cjfields at illinois.edu
Fri Jun 11 16:30:59 UTC 2010
My guess is that NCBI has something that does this internally, and the result is either cached or run on-the-fly. When I retrieved the full-length record from NCBI it lacked SNPs as well.
chris
On Jun 11, 2010, at 11:26 AM, Jessica Sun wrote:
> Great ! Yet, how do you add this SNP as an Feature tag named as Variation
> into the gbk file format automatically?
>
> thx
>
>
> On Thu, Jun 10, 2010 at 4:11 PM, Dave Messina <David.Messina at sbc.su.se>wrote:
>
>> Nice, Chris!
>>
>> I've added it to the EUtils cookbook.
>>
>> Dave
>>
>>
>>
>> On Jun 10, 2010, at 2:06 AM, Chris Fields wrote:
>>
>>> It's much easier to work with the GI than the accession. NCBI
>> unfortunately just recently 'broke' their acc->gi stuff via efetch; you have
>> to use rettype='seqid' and munge ASN.1 to get everything (though it is nice
>> in a way for ID mapping).
>>>
>>> After the initial step of grabbing the GI for NG_011506, though, you can
>> use elink to grab the SNP IDs, then use efetch to get the actual SNP files,
>> or esummary for the summary info.
>>>
>>> #!/usr/bin/perl -w
>>>
>>> use Modern::Perl;
>>> use Bio::DB::EUtilities;
>>>
>>> my $id = '224809339';
>>>
>>> my $eutil = Bio::DB::EUtilities->new(-eutil => 'elink',
>>> -id => $id,
>>> -email => 'setyourown at foo.bar',
>>> -verbose => 1,
>>> -dbfrom => 'nuccore',
>>> -db => 'snp',
>>> -cmd => 'neighbor_history',
>>> );
>>>
>>> my $hist = $eutil->next_History || die "No history data returned";
>>>
>>> $eutil->set_parameters(-eutil => 'efetch',
>>> -history => $hist,
>>> -retmode => 'text',
>>> # 'chr', 'flt', 'brief', 'rsr', 'docset'
>>> -rettype => 'chr'
>>> );
>>>
>>> $eutil->get_Response(-file => 'snps.txt');
>>>
>>> # or ...
>>>
>>> $eutil->set_parameters(-eutil => 'esummary',
>>> -history => $hist,
>>> );
>>>
>>> $eutil->print_all;
>>>
>>> # chris
>>>
>>> On Jun 9, 2010, at 1:37 PM, Jessica Sun wrote:
>>>
>>>> Thanks Dave.
>>>> the variation information is not present in the version of NG_011506 I
>> found
>>>> at Genbank.) -- Yes, then if you click on the right side customer view
>> there
>>>> is a check box Features added by NCBI :209 snps, if you check that it
>> will
>>>> add all the variations in the gbk fomat. I found this would be a neat
>>>> feature if it can automatically load by bioperl with an option turn on.
>>>>
>>>>
>>>>
>>>> On Wed, Jun 9, 2010 at 1:51 PM, Dave Messina <David.Messina at sbc.su.se
>>> wrote:
>>>>
>>>>> Hi Jessica,
>>>>>
>>>>> Please keep the BioPerl list on the Cc line so everyone can follow
>> along.
>>>>>
>>>>>
>>>>>> Follow your approach it did not seem to me you can have Variation tag
>>>>> included which
>>>>>> list the know dbSNP location, id and allele changes?
>>>>>
>>>>> Ah okay, I assumed the file you attached was obtained directly from
>> Genbank
>>>>> and that the variation info therein was already included. (It appears
>> that's
>>>>> not the case — the variation information is not present in the version
>> of
>>>>> NG_011506 I found at Genbank.)
>>>>>
>>>>> If you want to include your own custom information in a genbank file,
>>>>> you'll have to pull it out of dbSNP (or wherever the variation info
>> is).
>>>>> There are a couple of scripts that might be able to help with that
>> (search
>>>>> for snp):
>>>>>
>>>>> http://www.bioperl.org/wiki/Bioperl_scripts
>>>>>
>>>>>
>>>>> You can then insert them into a RichSeq object as features and output
>> in
>>>>> genbank format. For that part, see the HOWTO:
>>>>>
>>>>> http://www.bioperl.org/wiki/HOWTO:Feature-Annotation
>>>>>
>>>>>
>>>>> Dave
>>>>>
>>>>>
>>>>
>>>>
>>>> --
>>>> Jessica Jingping Sun
>>>>
>>>> _______________________________________________
>>>> Bioperl-l mailing list
>>>> Bioperl-l at lists.open-bio.org
>>>> http://lists.open-bio.org/mailman/listinfo/bioperl-l
>>>
>>
>>
>
>
> --
> Jessica Jingping Sun
>
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