genetica:bgscheme_all
Procedure for all tests
- First we took the every provided file (listTEST5.txt, listTEST6.txt, listTEST15.txt, listTEST16.txt) and look for the proxies for every marker at http://www.broadinstitute.org/mpg/snap/ldsearch.php with,
SNP data set: 1000 Genomes Pilot 1 r2 threshold: 0.7 Population panel: CEU Distance limit: 100
- We substitute every marker for all its proxies and construct every possible pair for each file
- Then, for every database, we choose the pairs which contains both makers in database. Aparently interSNP do this but it is very slow. We make this with a simple perl script. (download below)
- Now we run intersnp with the obtained pairs and each database. Here we run all those test using a template for the selection file and writing the tags as needed.
BFILE <Database> // put path and name of plink bfile there TWO_MARKER 1 PRINTTOP 50000 TEST <Test> COMBIFILE <Pairs> // if file is in working dir, else put path COMBILIST 1 OUTPUTNAME <Output> END
- Results and other files could be downloaded from https://docs.google.com/folder/d/0B8-42LJtMhdZSTVrZEZCU3d6NUE/edit
genetica/bgscheme_all.txt · Last modified: 2020/08/04 10:58 by 127.0.0.1