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6 bytes removed ,  00:21, 11 December 2012
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* When you have genotypes from ped and marker information from dat file, and assuming no relatedness in the sample:
 
* When you have genotypes from ped and marker information from dat file, and assuming no relatedness in the sample:
   −
   ./Rare-Metal-Worker --ped yours.ped --dat yours.dat
+
   ./raremetalworker --ped yours.ped --dat yours.dat
    
* When you have genotypes from vcf and covariates and trait information saved in ped and dat file, assuming there is no relatedness in the sample, you should use the following:
 
* When you have genotypes from vcf and covariates and trait information saved in ped and dat file, assuming there is no relatedness in the sample, you should use the following:
   −
   ./Rare-Metal-Worker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz
+
   ./raremetalworker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz
    
* When you have genotypes from vcf and covariates and trait information saved in ped and dat file, assuming there is cryptic relatedness in the sample, you should use the following:
 
* When you have genotypes from vcf and covariates and trait information saved in ped and dat file, assuming there is cryptic relatedness in the sample, you should use the following:
   −
   ./Rare-Metal-Worker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz --kinGeno (# this will handle individuals as related, and generate kinship matrix from genotype.)
+
   ./raremetalworker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz --kinGeno (# this will handle individuals as related, and generate kinship matrix from genotype.)
    
== Q & A ==
 
== Q & A ==
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