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OXFORD.PED
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1993-12-23
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oxford.ped Example of an Oxford format input file for CYRILLIC
R 16 2
loci
* Batten
A D16S159 16.17 ( 16 18 p122 ) < 3 >
B D16S294 16.28 ( 26 31 p12.1 ) < 2 >
Z
* S159 S294
Fam iden ind pat mat x a A B
1 2
103 pat 1 0 0 M C 3-3 2 1
103 mat 2 0 0 F C 2-1 1 2
103 Pa 3 1 2 . A 3-2 1 1
103 Pb 4 1 2 . A 3-1 2 2
999
Description of the Oxford format as implemented in CYRILLIC.
line 1 Description of the file contents. This line must be present but is used for documentation only.
line 2 Column 1 may contain either R, D, X, or C. These letters imply that the disease locus is recessive,
dominant, X-linked, or codominant respectively. This letter must be followed by one or more
spaces ant then the chromosome number, X, or Y. This is followed by any number of spaces,
and then the number of markers.
line 3 'loci' in columns 1-4.
line 4.... The marker names, which may use the format described in the section on inputting markers from files. The
minimum information is a letter in column 1, followed by one or more spaces and then
the name of the marker. Any line beginning with an * is assumed to contain the name of the disease locus
as the next item. Any other text on the line is ignored.
Z End of locus list. Must be a capital and in first column.
line n This is for documentation and may contain abbreviations for the markers to identify the columns.
line n+1 This can be used to identify the columns.
line n+2 This line can contain the locus order to be assumed. Note that CYRILLIC ignores lines n,n+1, and n+2, but they must be present.
Accordingly, they can be used for documentation. This means that the marker loci must be in
the order given by their order in the file.
lines n+3..... Family data. This is presented on one line per individual. The sequence is familyID; identifier (may
be pat, mat etc. but can be any space-free string of up to six characters and is added to the
CYRILLIC identifier field); fatherID, motherID, sex ( may be 1=Male, 2=Female,
.=unknown); affection status (0=unaffected, 1=affected, 2=unknown, c=carrier, a=affected,
u=unknown); followed byt the phenotypes. There must be as many phenotypes as there are
markers. The coding is either the LINKAGE numbered alleles format (i.e. two numbers
separated by one or more spaces giving the allele numbers), or two numbers separated by - .
Between families place a line starting with 0 ( zero ). The rest of the line is ignored and can be used for comments.
Last line of file Must start with "999 ".
After 999 any comments may be added for documentation.