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readme.pregsf90 [2019/07/26 21:52] – [Input files] ignacioreadme.pregsf90 [2019/09/04 17:31] – [Quality Control (QC) for G] ignacio
Line 89: Line 89:
 //SNP_ID// - identification of the SNP (alphanumeric) \\ //SNP_ID// - identification of the SNP (alphanumeric) \\
 //CHR// - chromosome number (numeric), starting from 1 \\ //CHR// - chromosome number (numeric), starting from 1 \\
-//POS// - position (bp) \\+//POS// - position bp (numeric) \\
  
 Extra columns are possible \\ Extra columns are possible \\
Line 101: Line 101:
 If ''OPTION saveCleanSNPs'' is present fields are output. If ''OPTION saveCleanSNPs'' is present fields are output.
  
-<file>OPTION chrinfo file </file> 
-OLD OPTION DEPRECATED \\ 
-Read SNP map information from //file//.\\ 
- 
-Useful for check for Mendelian conflicts and HWE (with also ''OPTION sex_chr'') and for GWAS (see ''PostGSF90'' program) 
- 
-Format, all numeric variables: //snp order , chromosome, position// (bp). 
- 
-//snp order// corresponds to the index number of the snp, in the sorted map by chromosome and position 
- 
- 
-//chromosome// should be only numbers and starting from 1 
-  
-First line in file corresponds to first SNP in genotype file, and so on. 
- 
-Other alphanumeric field are optional. 
- 
-If ''OPTION saveCleanSNPs'' is present fields are output. 
    
 =====Output files===== =====Output files=====
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 <file>OPTION excludeCHR n1 n2 n3 ...</file>  <file>OPTION excludeCHR n1 n2 n3 ...</file> 
 Exclude all SNP from chromosomes //n1 n2 n3// ...\\ Exclude all SNP from chromosomes //n1 n2 n3// ...\\
-Map file need to be provided. See ''OPTION chrinfo''+Map file need to be provided. See ''OPTION map_file''
  
 <file>OPTION includeCHR n1 n2 n3 ...</file>  <file>OPTION includeCHR n1 n2 n3 ...</file> 
 Include all SNP from chromosomes //n1 n2 n3// ...\\ Include all SNP from chromosomes //n1 n2 n3// ...\\
-Map file need to be provided. See ''OPTION chrinfo''+Map file need to be provided. See ''OPTION map_file''
  
 <file>OPTION excludeSample n1 n2 n3 ...</file>  <file>OPTION excludeSample n1 n2 n3 ...</file> 
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 <file>OPTION sex_chr n</file> <file>OPTION sex_chr n</file>
 Chromosomes number equal or greater than //n// are not consider autosomes.\\ Chromosomes number equal or greater than //n// are not consider autosomes.\\
-If selected this option, sex chromosomes will not be used for checking parent-progeny Mendelian conflicts and HWE\\+If selected this option, sex chromosomes will not be used for checking parent-progeny Mendelian conflicts,  HWE and heritability of gene content\\
 but they will be included for all remaining processes. **If you want to remove sex chromosomes**, which we do recommend, use ''OPTION excludeCHR''. but they will be included for all remaining processes. **If you want to remove sex chromosomes**, which we do recommend, use ''OPTION excludeCHR''.
    
-Map file need to be provided. See ''OPTION chrinfo''. However, note that sex chromosomes are not exlucded  +Map file need to be provided. See ''OPTION map_file''. However, note that sex chromosomes are not exlucded  
  
 <file>OPTION threshold_duplicate_samples x</file> <file>OPTION threshold_duplicate_samples x</file>
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 The test is useful for homogenous populations (breeds) but theory does not hold for crossbred animals.  The test is useful for homogenous populations (breeds) but theory does not hold for crossbred animals. 
  This test uses explicitly inv(A22) so it is not suitable for very large populations.  This test uses explicitly inv(A22) so it is not suitable for very large populations.
- 
  
  
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 OPTION readGmA22 [file]           OPTION readGmA22 [file]          
 </file> </file>
 +
 +=====DEPRECATED OPTIONS=====
 +<file>OPTION chrinfo file </file> \\
 +Read SNP map information from //file//.\\
 +
 +Useful for check for Mendelian conflicts and HWE (with also ''OPTION sex_chr'') and for GWAS (see ''PostGSF90'' program)
 +
 +Format, all numeric variables: //snp order , chromosome, position// (bp).
 +
 +//snp order// corresponds to the index number of the snp, in the sorted map by chromosome and position
 +
 +
 +//chromosome// should be only numbers and starting from 1
 + 
 +First line in file corresponds to first SNP in genotype file, and so on.
 +
 +Other alphanumeric field are optional.
 +
 +If ''OPTION saveCleanSNPs'' is present fields are output.
 +
readme.pregsf90.txt · Last modified: 2024/05/16 15:11 by dani

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