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, 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: |
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− | ./Rare-Metal-Worker --ped yours.ped --dat yours.dat | + | ./raremetalworker --ped yours.ped --dat yours.dat |
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| * 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: |
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− | ./Rare-Metal-Worker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz | + | ./raremetalworker --ped yours.ped --dat yours.dat --vcf yours.vcf.gz |
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| * 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: |
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− | ./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.) |
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| == Q & A == | | == Q & A == |