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===GENOTYPE field===
 
===GENOTYPE field===
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  0/0: homozygous reference chosen based on in PL.
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  0,9,108: PHRED scaled genotype likelihoods
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  9:  no. of reads covering this variant
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  3,0,6: allele depth
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          counts of reads supporting the reference allele, the alternative allele and neither.
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        The last category might be due to insufficient coverage of the read over the locus
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        or simply a mis specified allele.
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  10 :  genotype quality.
    
=Tools=
 
=Tools=
1,102

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