\name{read.snps.long} \alias{read.snps.long} \title{Read SNP data in long format} \description{ Reads SNP data when organized in free format as one call per line. Other than the one call per line requirement, there is considerable flexibility. Multiple input files can be read, the input fields can be in any order on the line, and irrelevant fields can be skipped. The samples and SNPs to be read must be pre-specified, and define rows and columns of an output object of class \code{"snp.matrix"}. } \usage{ read.snps.long(files, sample.id = NULL, snp.id = NULL, female = NULL, fields = c(sample = 1, snp = 2, genotype = 3, confidence = 4), codes = c("0", "1", "2"), threshold = 0.9, lower = TRUE, sep = " ", comment = "#", skip = 0, simplify = c(FALSE,FALSE), verbose = FALSE, in.order=TRUE, every = 1000) } %- maybe also 'usage' for other objects documented here. \arguments{ \item{files}{A character vector giving the names of the input files} \item{sample.id}{A character vector giving the identifiers of the samples to be read} \item{snp.id}{A character vector giving the names of the SNPs to be read} \item{female}{If the SNPs are on the X chromosome and the data are to be read as such, this logical vector (of the same length as \code{sample.id} should specify whether each sample was from a female subject} \item{fields}{A integer vector with named elements specifying the positions of the required fields in the input record. The fields are identified by the names \code{sample} and \code{snp} for the sample and SNP identifier fields, \code{confidence} for a call confidence score (if present) and either \code{genotype} if genotype calls occur as a single field, or \code{allele1} and \code{allele2} if the two alleles are coded in different fields} \item{codes}{Either the single string \code{"nucleotide"} denoting that coding in terms of nucleotides (\code{A}, \code{C}, \code{G} or \code{T}, case insensitive), or a character vector giving genotype or allele codes (see below)} \item{threshold}{A numerical value for the calling threshold on the confidence score} \item{lower}{If \code{TRUE}, then \code{threshold} represents a lower bound. Otherwise it is an upper bound} \item{sep}{The delimiting character separating fields in the input record} \item{comment}{A character denoting that any remaining input on a line is to be ignored} \item{skip}{An integer value specifying how many lines are to be skipped at the beginning of each data file} \item{simplify}{If \code{TRUE}, sample and SNP identifying strings will be shortened by removal of any common leading or trailing sequences when they are used as row and column names of the output \code{snp.matrix} } \item{verbose}{If \code{TRUE}, a progress report is generated as every \code{every} lines of data are read} \item{in.order}{If \code{TRUE}, input lines are assumed to be in the correct order (see details)} \item{every}{See \code{verbose}} } \details{ If nucleotide coding is not used, the \code{codes} argument should be a character array giving the valid codes. For genotype coding of autosomal SNPs, this should be an array of length 3 giving the codes for the three genotypes, in the order homozygous(AA), heterozygous(AB), homozygous(BB). All other codes will be treated as "no call". The default codes are \code{"0"}, \code{"1"}, \code{"2"}. For X SNPs, males are assumed to be coded as homozygous, unless an additional two codes are supplied (representing the AY and BY genotypes). For allele coding, the \code{codes} array should be of length 2 and should specify the codes for the two alleles. Again, any other code is treated as "missing" and, for X SNPs, males should be coded either as homozygous or by omission of the second allele. For nucleotide coding, nucleotides are assigned to the nominal alleles in alphabetic order. Thus, for a SNP with either "T" and "A" nucleotides in the variant position, the nominal genotypes AA, AB and BB will refer to A/A, A/T and T/T. Although the function allows for reading of data for the X chromosome directly into an object of class \code{"X.snp.matrix"}, it will often be preferable to read such data as a \code{"snp.matrix"} (i.e. as autosomal) and to coerce it to an object of type \code{"X.snp.matrix"} later using \code{as(..., "X.snp.matrix")} or \code{new("X.snp.matrix", ..., female=...)}. If sex is coded \code{NA} for any subject the latter course \emph{must} be followed, since \code{NA}s are not accepted in the \code{female} argument. If the \code{in.order} argument is set \code{TRUE}, then the vectors \code{sample.id} and \code{snp.id} must be in the same order as they vary on the input file(s) and this ordering must be consistent. However, there is no requirement that either SNP or sample should vary fastest as this is detected from the input. If \code{in.order} is \code{FALSE}, then no assumptions about the ordering of the input file are assumed and SNP and sample identifiers are looked up in hash tables as they are read. This option must be expected, therefore, to be somewhat slower. Each file may represent a separate sample or SNP, in which case the appropriate \code{.id} argument can be omitted; row or column names are then taken from the file names. } \value{ An object of class \code{"snp.matrix"} or \code{"X.snp.matrix"}. } \note{ The function will read gzipped files. If \code{in.order} is \code{TRUE}, every combination of sample and snp listed in the \code{sample.id} and \code{snp.id} arguments \emph{must} be present in the input file(s). Otherwise the function will search for any missing observation until reaching the end of the data, ignoring everything else on the way. } \author{David Clayton \email{david.clayton@cimr.cam.ac.uk}} \seealso{\code{\link{read.HapMap.data}}\code{\link{read.snps.pedfile}}, \code{\link{read.snps.chiamo}}, \code{\link{read.plink}}, \code{\link{snp.matrix-class}}, \code{\link{X.snp.matrix-class}}} \keyword{manip} \keyword{IO} \keyword{file} \keyword{utilities}