[BioC] VariantAnnotation: readVcf on nonmodel organism
Yannick Wurm
y.wurm at qmul.ac.uk
Wed Sep 26 21:01:46 CEST 2012
Ha that's hilarious! I wouldn't have thunk it could be so easy!
thanks Sean & Valerie!!
yannick
On 26 Sep 2012, at 19:49, Valerie Obenchain wrote:
> Hi Yannick,
>
> The 'genome' argument to readVcf() is a character string specifying the build of the genome the variants are mapped to. It's present use is for your own bookkeeping so there are no "invalid" strings. In this case using the build that is on NCBI would be logical or you could use your own tag,
>
> readVcf("mymappings.vcf.gz", "draftgenome")
>
> Valerie
>
>
> On 09/26/2012 10:56 AM, Yannick Wurm wrote:
>> Dear list,
>>
>> I work with a non-model organism (an ant) for which we sequenced the genome. The genome is on NCBI but isn't annotated in the standard R-accessible databases.
>>
>> I'm now trying to load a VCF file into R (with the aim of subsequent plotting with ggbio).
>>
>>> library(VariantAnnotation)
>>> readVcf("mymappings.vcf.gz")
>> This fails because readVcf wants a "genome" argument. I haven't been able to find an example using a non-established genome. How can I generate such a genome for my species? The genome is in the form of 10,000 scaffolds. I'm looking for a quick hack, not a complex submission to another database.
>>
>> FWIW This is on R 2.15.0 with latest bioconductor.
>>
>> Thanks for your help& kind regards,
>>
>> Yannick
>>
>>
>>
>>
>>
>> --------------------------------------
>> Yannick Wurm http://yannick.poulet.org
>> Ants, Genomes& Evolution ⋅ y.wurm at qmul.ac.uk ⋅ skype:yannickwurm ⋅ +44 207 882 3049
>> 5.03A Fogg ⋅ School of Biological& Chemical Sciences ⋅ Queen Mary, University of London ⋅ Mile End Road ⋅ E1 4NS London ⋅ UK
>> Easy custom BLAST interface: http://www.sequenceserver.com
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