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Revision as of 11:16, 27 September 2010
, 11:16, 27 September 2010→Input
<pre> --chr # --start <base position> --end <base position> </pre>
<pre> --chr # --start <base position> --end <base position> </pre>
The SNP with the most significant p-value in this region will be used for estimating LD.
The SNP with the most significant p-value in this region will be used for estimating LD.
=== Specifying LD source/population/build ===
We supply genotype files for computing LD between the reference SNP and all other SNPs within the region you are plotting. Currently, we support:
=== Batch mode ===
=== Batch mode ===
