Option | Parameter | Description |
--file | {fileroot} | Specify .ped and .map files |
--ped | {pedfile} | Specify .ped file |
--map | {mapfile} | Specify .map file |
--bfile | {fileroot} | Specify .bed, .fam and .map |
--pheno | {phenofile} | Specify .phe file |
--cov | {covarfile} | Specify .cov file |
--output | {fileroot} | Specify output root filename |
--out | {fileroot} | Specify output root filename |
|
--make-bed | | Make .bed, .fam and .bim |
--extract | {snplist} | Extract list of SNPs |
--remove | {indlist} | Remove these individuals |
--recode | | Output new PED and MAP files |
--recode12 | | As above, with 1/2 alleles |
--merge | {pedfile} {mapfile} | Merge two PED/MAP files |
--restrand | | Flip all SNPs |
--flip | {snplist} | Flip strand of SNPs in list |
|
--maf | {0.02} | Minor allele frequency |
--geno | {0.1} | Maximum per-SNP missing |
--mind | {0.1} | Maximum per-person missing |
--cell | {5} | Minimum genotype cell count for --model |
|
--freq | | Save allele frequencies |
--missing | | Missing rates (per individual/SNP) |
--hardy | | Hardy-Weinberg disequilibrium tests |
|
--perm | {1000} | # of permutations |
--within | | Within cluster permutation |
--family | | Make Family ID the cluster |
--within-file | {file} | File containing clusters |
|
--missing-genotype | {0} | Missing genotype code |
--missing-phenotype | {-9} | Missing phenotype code |
--ignore | | Do not perform analysis |
--genome | | Output genome-wide IBS |
--inbreeding | | Individual inbreeding |
--homo-run | N | |
--homo-run-snps | N | |
--local-homo | N | sliding window of homozygosity |
--test-missing | |
|
--cluster | | Perform clustering |
--matrix | | Output distance matrices |
--mc | {0} | Maximum cluster size |
--cc | | Cluster by phenotype |
--sol | {N} | Only analyse these subjects |
--pmerge | {0.01} | Cluster merge value |
--ibs | | Cluster on IBS, not p-value |
|
--assoc | | Case/control, QT association |
--model | | Full-model C/C association |
--tdt | | Family-based TDT association |
--parentdt1 | | |
--parentdt2 | | |
|
--epistasis | | |
--case-only | | |
--epi1 | {0.0001} | |
--epi2 | {0.01} | |
--set-by-all | | |
--genepi | | |
--R | | |
--nop | | |
|
--tag | {tagfilename} | Multimarker predictor list |
--hap | {tagfilename} | Multimarker predictor list |
--r | | Matrix of LD stats (r) |
--r2 | | Matrix of LD stats (r^2) |
|
--set | {setfilename} | SET definitions |
|
--sharing | | IBS-based association |
--boot | | Bootstrap z-scores |
--help | | Display this list |
Filename | Description |
plink.assoc | Association results, with permutation |
plink.cluster0 | Progress of IBS clustering |
plink.cluster1 | IBS cluster solution, format 1 |
plink.cluster2 | IBS cluster solution, format 2 |
plink.cluster3 | IBS cluster solution, format 3 |
plink.mdist | IBS distance matrix |
plink.pdist | p-value distance matrix |
plink.imiss | Missing rates, per individual |
plink.lmiss | Missing rates, per locus |
plink.imendel | Mendel errors, per family |
plink.lmendel | Mendel errors, per locus |
plink.het | Individual inbreeding coefficients |
plink.ihet | Runs of homozygosity |
plink.frq | Allele frequency table |
plink.hwe | Hardy-Weinberg test statistics |
plink.tdt.asym | TDT/parenTDT asymptotic results |
plink.tdt.perm | TDT/parenTDT permutaion results |
plink.qassoc | Quantitative trait association results |
plink.model | Full-model association results |
plink.genome | Genome-wide IBD/IBS pairwise measures |
plink-recode.ped | Recoded PED file |
plink-recode.map | Recoded MAP file |
plink-extract.ped | Extracted PED file |
plink-extract.map | Extracted MAP file |
plink.epi-cc1 | Epistasis: case/control pairwise results |
plink.epi-cc2 | Epistasis: case/control summary results |
plink.epi-co1 | Epistasis: case-only pairwise results |
plink.epi-co2 | Epistasis: case-only summary results |
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