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| # RG : ReadGroup ID of sequenced lane. For [outPrefix].selfSM and [outPrefix].bestSM, these values are "ALL" | | # RG : ReadGroup ID of sequenced lane. For [outPrefix].selfSM and [outPrefix].bestSM, these values are "ALL" |
| * CHIP_ID : Sample ID compared to in the genotype file. For [outPrefix].selfRG and [outPrefix].selfSM, these values should be identical to [SEQ_SM] or "NA" if the genotype of sequenced samples are unavailable. For [outPrefix].bestRG and [outPrefix].bestSM, these values should be the ID of best-matching sample among the genotype files compared to. | | * CHIP_ID : Sample ID compared to in the genotype file. For [outPrefix].selfRG and [outPrefix].selfSM, these values should be identical to [SEQ_SM] or "NA" if the genotype of sequenced samples are unavailable. For [outPrefix].bestRG and [outPrefix].bestSM, these values should be the ID of best-matching sample among the genotype files compared to. |
− | * # SNPs : # of SNPs passing the criteria from the VCF file
| + | # # SNPs : # of SNPs passing the criteria from the VCF file |
− | * # READS : Total # of reads loaded from the BAM file
| + | # # READS : Total # of reads loaded from the BAM file |
− | * # AVG_DP : Average sequencing depth at the sites in the VCF file
| + | # # AVG_DP : Average sequencing depth at the sites in the VCF file |
− | * FREEMIX : Sequence-only estimate of contamination
| + | # FREEMIX : Sequence-only estimate of contamination |
− | * FREELK1 : Maximum log-likelihood of the sequence reads given estimated contamination under sequence-only method
| + | # FREELK1 : Maximum log-likelihood of the sequence reads given estimated contamination under sequence-only method |
− | * FREELK0 : Log-ikelihood of the sequence reads given no contamination under sequence-only method
| + | # FREELK0 : Log-ikelihood of the sequence reads given no contamination under sequence-only method |
− | * FREE_RH : Estimated reference bias parameter Pr(refBase|HET) (when --free-refBias or --free-full is used)
| + | # FREE_RH : Estimated reference bias parameter Pr(refBase|HET) (when --free-refBias or --free-full is used) |
− | * FREE_RA : Estimated reference bias parameter Pr(refBase|HOMALT) (when --free-refBias or --free-full is used)
| + | # FREE_RA : Estimated reference bias parameter Pr(refBase|HOMALT) (when --free-refBias or --free-full is used) |
− | * CHIPMIX : Sequence+array estimate of contamination (NA if the external genotype is unavailable)
| + | # CHIPMIX : Sequence+array estimate of contamination (NA if the external genotype is unavailable) |
− | * CHIPLK1 : Maximum log-likelihood of the sequence reads given estimated contamination under sequence+array method (NA if the external genotypes are unavailable)
| + | # CHIPLK1 : Maximum log-likelihood of the sequence reads given estimated contamination under sequence+array method (NA if the external genotypes are unavailable) |
− | * CHIPLK0 : Log-likelihood of the sequence reads given no contamination under sequence+array method (NA if the external genotypes are unavailable)
| + | # CHIPLK0 : Log-likelihood of the sequence reads given no contamination under sequence+array method (NA if the external genotypes are unavailable) |
− | * CHIP_RH : Estimated reference bias parameter Pr(refBase|HET) (when --chip-refBias or --chip-full is used)
| + | # CHIP_RH : Estimated reference bias parameter Pr(refBase|HET) (when --chip-refBias or --chip-full is used) |
− | * CHIP_RA : Estimated reference bias parameter Pr(refBase|HOMALT) (when --chip-refBias or --chip-full is used)
| + | # CHIP_RA : Estimated reference bias parameter Pr(refBase|HOMALT) (when --chip-refBias or --chip-full is used) |
| # DPREF : Depth (Coverage) of HomRef site (based on the genotypes of (SELF_SM/BEST_SM), passing mapQ, baseQual, maxDepth thresholds. | | # DPREF : Depth (Coverage) of HomRef site (based on the genotypes of (SELF_SM/BEST_SM), passing mapQ, baseQual, maxDepth thresholds. |
| # RDPHET : DPHET/DPREF, Relative depth at Heterozygous site. | | # RDPHET : DPHET/DPREF, Relative depth at Heterozygous site. |