Differences

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--- readme.illumina2pregs [2014/05/26 09:56] – [Illumina2preGS] ignacio
+++ readme.illumina2pregs [2017/04/12 02:38] – [Output files] dani
@@ Line 10: / Line 10: @@
 ======Summary======
-Tool for converts FinalReport files from Genome Studio into file suitable for reading with ''pregsf90''
+Tool for converting ''FinalReport'' and ''SNP_Map.txt'' files from Genome Studio into files suitables for reading with ''pregsf90''
-Read only AB codes and generates integer variable 0,1,2  or 5 for missing
+Reads only AB codes and generates integer variable 0,1,2  or 5 for missing
 ======Usage======
-<file>illumina2pregs --snpfile <yourSnpFinalReportFilename> </file>
+<file>illumina2preGS --snpfile <yourSnpFinalReportFilename> </file>
 The only mandatory argument that is required is the ''--snpfile''
@@ Line 23: / Line 24: @@
 =====Optional Arguments=====
 <file>--mapfile</file>
-      - File name for the map file. Default "SNP_Map.txt"
+ File name for the map file. Default "SNP_Map.txt"
 <file>--genome</file>
-       - Indicate type of genome (1 - bovine, 2 - ovine)
+ Indicate type of genome (1 - bovine, 2 - ovine)
 <file>--nosortmap</file>
-    - Genotype file will be in the same order as given
+ Genotype file will be in the same order as given
 <file>--codeab  <n></file>
-  - Indicate column number for the first allele with code AB (defalut 7)
+ Indicate column number for the first allele with code AB (defalut 7)
 <file>--gc  <n thr></file>
-  - Set column number (n) of GC and the cutoff (thr) for exclude call (default from GenomeStudio 0.15)
+ Set column number (n) of GC and the cutoff (thr) for exclude call (default from GenomeStudio 0.15)
 <file>--alphasize</file>
-    - Set the maximun length to store alphnumeric IDs (default 10)
+ Set the maximun length to store alphanumeric IDs (default 10)
 <file>--snpfile_out</file>
-  - Set a file name for output SNP file (default snps2pregs)
+ Set a file name for output SNP file (default snps2pregs)
 =====File formats=====
-Input files
+====Input files====
------------
+''SNP_Map.txt''
-SNP_Map.txt:
 Index
 Name
@@ Line 56: / Line 56: @@
 NormID
-FinalReport.txt:
+''FinalReport.txt''
-** this is the default but use --codeab for change it
 SNP_Name
 Sample ID
@@ Line 70: / Line 70: @@
 Y
-Output files:
+** this is the default column position but you can use ''--codeab'' argument for change it the column for
--------------
+====Output files====
-snps2pregs:
+''snps2pregs''
   ID (alphnumeric identification of lenght "alphasize", default 10)
   one space
   genotypes: 0, 1, 2, for AA, AB and BB respectively and 5 for missing.
-snp_map:
+''snp_map''
 index
 chromosome
@@ Line 85: / Line 86: @@
 index in original SNP_Map.txt
+SNP without defined position (CRH = 0) in the SNP_Map.txt will be located in a new CHR 32 in the output snp_map, but still with 0 position.