combine genotype experiments

This could be done in the select lines by "genotype" page. Limit combining to same platform (9K, 90K, GBS). In cases where lines duplicate, the name can be altered (_duplicate)

Decided to combine 2 genotype experiments into 1 experiment then we will not need to change tools

install Ubuntu 14.04 on tcap machine. We need to allocate several days when no updates are allowed on production machine

operating system upgrade scheduled for weekend of Feb 19th

plan on adding a new server this summer

1. merging lines with 50% genotype conflicts (these are not the same line)
2. Nick/Shiaoman (haplotag) will submit VCF file (Oat)
3. others? Jeffery (Kevin from MN), Rich (Barley 9K ND)

1. added link for JBrowse, marker, and trial count
2. added trait description and ontology
3. added QTLs from imputed genotypes
4. added grouping by marker and gene
5. how to combine p values? Do you through out disease trials? Do we need confidence interval for qtl loci?

1. email still not delivered to some sites because of USDA limitations