On Dec 9, 2011, at 2:44 AM, Scott Harding wrote:
> Hi all,
>
> We are using two methods to identify SNPs. One is based on
> resequencing
> the genome and aligning the reads to the sequenced genome to
> identify SNPs
> (data available for 44 individuals). Another is based on SNP array
> with
> selected loci (30000 loci, 870 individuals). I want to compare the
> results
> from the resequencing based minor allele frequency and Array based
> minor
> allele frequency. What statistical test should I use?
>
> My table looks like
>
> Chromosome position Major/minor
> Resequencing SNP array
>
> chromosome 1 198432 C/T
> 75/13 1460/280
> chromosome 1 14282752 A/G
> 69/19 1380/360
> chromosome 1 595434 T/G
> 83/5 1680/60
>
>
> I really appreciate any guidance.
You will get a much more knowledgeable audience about such questions
(or at least the currently accepted strategies in your domain) when
you post this on the Bioconductor mailing list.
>
> Thanks
> Scott
>
> [[alternative HTML version deleted]]
I suspect they are also maintaining an HTML-free zone, but I don't
know for sure. R-help at any rate is an HTML-free mailing list, but
this post would get encapsulated in the archives in a strange little
wrapper that requires extra clicking to navigate:
https://stat.ethz.ch/pipermail/r-help/2011-December/298087.html
--
David Winsemius, MD
West Hartford, CT