pacoxph (1)

pacoxph [ command-line options ]

pacoxph runs a linear regression on large imputed data sets in an efficient way.

Required command line options

-p, -\^-pheno FILE

Read phenotype data from FILE

-i, -\^-info FILE

Read SNP information from FILE (e.g. MLINFO file).

-d, -\^-dose FILE

SNP predictor (e.g. MLDOSE/MLPROB) file name.

Optional command line options

-m, -\^-map FILE

Map file name, containing base pair positions for each SNP.

-n, -\^-nids NUMBER

Number of people to analyse.

-c, -\^-chrom FILE

Chromosome (to be passed to output).

-o, -\^-out FILE

Output file name (default is regression.out.txt ).

-s, -\^-skipd NUMBER

How many columns to skip in predictor (dose/prob) file (default is 2).

-t, -\^-ntraits NUMBER

How many traits are analysed (default is 2).

-g, -\^-ngpreds NUMBER

How many predictor columns per marker (default 1 = MLDOSE; else use 2 for MLPROB).

-a, -\^-separat FILE

Character to separate fields (default is space).

-r, -\^-score

Use the score test.

-e, -\^-no-head

Do not report header line in the output.

-l -\^-allcov

Report estimates for all covariates (large outputs!).

-b, -\^-interaction

Which covariate to use for interaction with SNP analysis (default is no interaction, 0).

-k, -\^-interaction_only

Like -\^-interaction but without covariate acting in interaction with SNP (default is no interaction, 0).

-\^-help

Print help.

palinear(1), palogist(1)

The bugtracker is located at

https://r-forge.r-project.org/tracker/?group_id=505

Lennart C. Karssen