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--- readme.illumina2pregs [2014/05/26 09:48] – created ignacio
+++ readme.illumina2pregs [2017/03/16 18:58] – [Summary] dani
@@ Line 1: / Line 1: @@
-=====illumina2pregs=====
+====== Illumina2preGS ======
- - a program to convert genomic information
+ A program to convert genomic information from Illumina files for the BLUPF90 family of programs\\
-                 from Illumina files for the BLUPF90 family of programs
  Ignacio Aguilar - INIA Las Brujas
  email: iaguilar at inia.org.uy
 /10/11 - 06/16/12
 ======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
-======USAGE======
+Reads only AB codes and generates integer variable 0,1,2  or 5 for missing
-   <file>illumina2pregs --snpfile <yourSnpFinalReportFilename> </file>
-   the only mandatory argument that is required is the --snpfile
+======Usage======
-   other options can be modified with optional arguments:
-Optional Arguments
+<file>illumina2preGS --snpfile <yourSnpFinalReportFilename> </file>
-  --mapfile      - File name for the map file. Default "SNP_Map.txt"
-  --genome       - Indicate type of genome (1 - bovine, 2 - ovine)
-  --nosortmap    - Genotype file will be in the same order as given
-  --codeab  <n>  - Indicate column number for the first allele with code AB (defalut 7)
-  --gc  <n thr>  - Set column number (n) of GC and the cutoff (thr) for exclude call (default from GenomeStudio 0.15)
-  --alphasize    - Set the maximun length to store alphnumeric IDs (default 10)
-  --snpfile_out  - Set a file name for output SNP file (default snps2pregs)
+The only mandatory argument that is required is the ''--snpfile''
-File formats:
+Other options can be modified with optional arguments:
-=============
-Input files
+=====Optional Arguments=====
------------
+<file>--mapfile</file>
-SNP_Map.txt:
+ File name for the map file. Default "SNP_Map.txt"
+<file>--genome</file>
+ Indicate type of genome (1 - bovine, 2 - ovine)
+<file>--nosortmap</file>
+ 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)
+<file>--gc  <n thr></file>
+ 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 alphanumeric IDs (default 10)
+<file>--snpfile_out</file>
+ Set a file name for output SNP file (default snps2pregs)
+=====File formats=====
+====Input files====
+''SNP_Map.txt''
 Index
 Name
@@ Line 46: / Line 56: @@
 NormID
-FinalReport.txt:
+''FinalReport.txt''
-** this is the default but use --codeab for change it
 SNP_Name
 Sample ID
@@ Line 60: / 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