| readPed | R Documentation | 
Reads a text file in pedigree format, or something fairly close to it.
readPed(
  pedfile,
  colSep = "",
  header = NA,
  famid_col = NA,
  id_col = NA,
  fid_col = NA,
  mid_col = NA,
  sex_col = NA,
  marker_col = NA,
  locusAttributes = NULL,
  missing = 0,
  sep = NULL,
  colSkip = NULL,
  sexCodes = NULL,
  addMissingFounders = FALSE,
  validate = TRUE,
  ...
)
| pedfile | A file name | 
| colSep | A column separator character, passed on as the  | 
| header | A logical. If NA, the program will interpret the first line as a header line it contains both "id" and "sex" as part of some entries (ignoring case). | 
| famid_col | Index of family ID column. If NA, the program looks for a column named "famid" (ignoring case). | 
| id_col | Index of individual ID column. If NA, the program looks for a column named "id" (ignoring case). | 
| fid_col | Index of father ID column. If NA, the program looks for a column named "fid" (ignoring case). | 
| mid_col | Index of mother ID column. If NA, the program looks for a column named "mid" (ignoring case). | 
| sex_col | Index of column with gender codes (0 = unknown; 1 = male; 2 = female). If NA, the program looks for a column named "sex" (ignoring case). If this is not found, genders of parents are deduced from the data, leaving the remaining as unknown. | 
| marker_col | Index vector indicating columns with marker alleles. If NA,
all columns to the right of all pedigree columns are used. If  | 
| locusAttributes | Passed on to  | 
| missing | Passed on to  | 
| sep | Passed on to  | 
| colSkip | Columns to skip, given as a vector of indices or columns
names. If given, these columns are removed directly after  | 
| sexCodes | A list with optional entries "male", "female" and "unknown",
indicating how non-default entries in the  | 
| addMissingFounders | A logical. If TRUE, any parent not included in the
 | 
| validate | A logical indicating if the pedigree structure should be validated. | 
| ... | Further parameters passed on to  | 
If there are no headers, and no column information is provided by the user, the program assumes the following column order:
family ID (optional; guessed from the data)
individual ID
father's ID
mother's ID
sex
marker data (remaining columns)
Adding the argument locusAttributes = "snp-AB", sets all markers to be
equifrequent SNPs with alleles A and B. Moreover, the letters A and B may be
replaced by other single-character letters or numbers, e.g., "snp-12" gives
alleles 1 and 2.
A ped object or a list of such.
tf = tempfile()
### Write and read a trio
trio = data.frame(id = 1:3, fid = c(0,0,1), mid = c(0,0,2), sex = c(1,2,1))
write.table(trio, file = tf, row.names = FALSE)
readPed(tf)
# With marker data in one column
trio.marker = cbind(trio, M = c("1/1", "2/2", "1/2"))
write.table(trio.marker, file = tf, row.names = FALSE)
readPed(tf)
# With marker data in two allele columns
trio.marker2 = cbind(trio, M.1 = c(1,2,1), M.2 = c(1,2,2))
write.table(trio.marker2, file = tf, row.names = FALSE)
readPed(tf)
### Two singletons in the same file
singles = data.frame(id = c("S1", "S2"),
                     fid = c(0,0), mid = c(0,0), sex = c(2,1),
                     M = c("9/14.2", "9/9"))
write.table(singles, file = tf, row.names = FALSE)
readPed(tf)
### Two trios in the same file
trio2 = cbind(famid = rep(c("trio1", "trio2"), each = 3), rbind(trio, trio))
# With column names
write.table(trio2, file = tf, col.names = TRUE, row.names = FALSE)
readPed(tf)
# Without column names
write.table(trio2, file = tf, col.names = FALSE, row.names = FALSE)
readPed(tf)
### With non-standard `sex` codes
trio3 = data.frame(id = 1:3, fid = c(0,0,1), mid = c(0,0,2),
                   sex = c("male","female","?"))
write.table(trio3, file = tf, row.names = FALSE)
readPed(tf, sexCodes = list(male = "male", female = "female", unknown = "?"))
# Cleanup
unlink(tf)
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