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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], \ | + | lanecheck --referencegenome /usr/cluster/share/karma/NCBI36.fa --dbSNPfile /home/1000G/data/GenomeSNP.dbsnp, \ |
− | --dbSNPfile [/home/1000G/data/GenomeSNP.dbsnp], \
| + | --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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| | | |
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| === Input Files === | | === Input Files === |
| | | |
− | -f ''genotype likelihood file'' Father's [[GLF|GLF]]-format genotype likelihood file | + | lanecheck Input Files : --referencegenome [/usr/cluster/share/karma/NCBI36.fa], \ |
− | -m ''genotype likelihood file'' Mother's [[GLF|GLF]]-format genotype likelihood file | + | --dbSNPfile [/home/1000G/data/GenomeSNP.dbsnp], \ |
− | -c ''genotype likelihood file'' Child's [[GLF|GLF]]-format genotype likelihood file | + | --lanefile [], --pedfile [], --datfile [], --mapfile [], \ |
| + | --mapquality [-1], --genocount [1000000], --nonrefhomo, \ |
| + | --verbose, --coverage, --countbysite, --memorymap \ |
| + | Output Files : --prefix [] |
| + | |
| + | --referencegenome ''genotype likelihood file'' |
| + | --dbSNPfile ''genotype likelihood file'' |
| + | --lanefile ''genotype likelihood file'' |
| + | --pedfile |
| + | --datfile |
| + | --mapfile |
| + | |
| | | |
| === Basic Output Options === | | === Basic Output Options === |
| | | |
− | -b ''baseCallFile'' Specifies the name of the output [[VCF|VCF]]-format base call file
| + | 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.
| + | 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. |