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535 bytes added ,  17:51, 22 November 2009
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Here is an example of how <code>glfTrio</code> works:
 
Here is an example of how <code>glfTrio</code> works:
   −
   lanecheck     Input Files : --referencegenome [/usr/cluster/share/karma/NCBI36.fa], \
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   lanecheck --referencegenome /usr/cluster/share/karma/NCBI36.fa --dbSNPfile /home/1000G/data/GenomeSNP.dbsnp,  \
                  --dbSNPfile [/home/1000G/data/GenomeSNP.dbsnp],  \
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            --lanefile lane.lst --pedfile test.ped --datfile test.dat --mapfile test.map --prefix result
                  --lanefile [], --pedfile [], --datfile [], --mapfile [], \
  −
                  --mapquality [-1], --genocount [1000000], --nonrefhomo, \
  −
                  --verbose, --coverage, --countbysite, --memorymap \
  −
  Output Files : --prefix []
   
   
 
   
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=== Input Files ===
 
=== Input Files ===
   −
  -f ''genotype likelihood file''    Father's [[GLF|GLF]]-format genotype likelihood file
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  lanecheck Input Files : --referencegenome [/usr/cluster/share/karma/NCBI36.fa], \
  -m ''genotype likelihood file''    Mother's [[GLF|GLF]]-format genotype likelihood file
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              --dbSNPfile [/home/1000G/data/GenomeSNP.dbsnp],  \
  -c ''genotype likelihood file''    Child's [[GLF|GLF]]-format genotype likelihood file
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              --lanefile [], --pedfile [], --datfile [], --mapfile [], \
 +
                  --mapquality [-1], --genocount [1000000], --nonrefhomo, \
 +
                  --verbose, --coverage, --countbysite, --memorymap \
 +
  Output Files : --prefix []
 +
 +
--referencegenome ''genotype likelihood file'' 
 +
  --dbSNPfile ''genotype likelihood file''     
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  --lanefile ''genotype likelihood file''     
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--pedfile
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--datfile
 +
--mapfile
 +
    
=== Basic Output Options ===
 
=== Basic Output Options ===
   −
  -b ''baseCallFile''                Specifies the name of the output [[VCF|VCF]]-format base call file
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lanecheck    Input Files : --referencegenome [/usr/cluster/share/karma/NCBI36.fa], \
 +
                  --dbSNPfile [/home/1000G/data/GenomeSNP.dbsnp],  \
 +
                  --lanefile [], --pedfile [], --datfile [], --mapfile [], \
 +
                  --mapquality [-1], --genocount [1000000], --nonrefhomo, \
 +
                  --verbose, --coverage, --countbysite, --memorymap \
 +
  Output Files : --prefix []
 +
 +
 +
-b ''baseCallFile''                Specifies the name of the output [[VCF|VCF]]-format base call file
 
  -p ''threshold''                  The threshold for base calling. Base calls will be made when their posterior likelihood exceeds ''threshold''
 
  -p ''threshold''                  The threshold for base calling. Base calls will be made when their posterior likelihood exceeds ''threshold''
 
  --reference                    Positions called as homozygous reference will be included in the output.   
 
  --reference                    Positions called as homozygous reference will be included in the output.   
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   --minMapQuality ''threshold''      Positions where the root-means squared mapping quality falls below this threshold will be excluded.
 
   --minMapQuality ''threshold''      Positions where the root-means squared mapping quality falls below this threshold will be excluded.
 
  --strict                      When the map quality is interpreted ''strictly'', all three trio individuals must exceed ''minMapQuality''  
 
  --strict                      When the map quality is interpreted ''strictly'', all three trio individuals must exceed ''minMapQuality''  
                            before a call is made. Without the --strict option, reads for individuals below the threshold are ignored.
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                            before a call is made. Without the --strict option, reads for individuals below the threshold are ignored.
    
   --minTotalDepth ''threshold''          Positions where the read depth falls below this threshold will be excluded.
 
   --minTotalDepth ''threshold''          Positions where the read depth falls below this threshold will be excluded.
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