ANGSD: Analysis of next generation Sequencing Data

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Genotype calling

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Revision as of 15:17, 18 June 2012 by Albrecht (talk | contribs) (Created page with "==Genotype calling== output file .geno -doGeno 1, print out major minor -doGeno 2, print the called genotype under HWE (suyeon maf prior method) -doGeno 4, print out the g...")
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Genotype calling

output file .geno


-doGeno 1, print out major minor

-doGeno 2, print the called genotype under HWE (suyeon maf prior method)

-doGeno 4, print out the genotype with the best raw likelihood

-doGeno 8, print out the posteriour under the suyeon model

-doGeno 16, print all 3 posts (major,major),(major,minor),(minor,minor)

-doGeno 32, print the depth, (if availble), the number of reads used to determine the genotype llhs.

-doGeno 64, somewhat different dumps the binary posts for all samples, encoded as 3*nind double

The genotype are integers such that AA=0,AC=1,AG=2,AT=3,CC=4,CG=5,CT=6,GG=7,GT=8,TT=9

output is (-doGeno NOT 64) chr, pos, numberof samples times[ the above]


NB currently you also need to supply -doMaf to run this genotype calling