# HG changeset patch # User bcrain-completegenomics # Date 1337886921 14400 # Node ID fec197eb2f00ecb2db7bc269635a08abbb0292c8 # Parent 8caa26b33983adcb0314a89feb51d75db957c0b2 Uploaded diff -r 8caa26b33983 -r fec197eb2f00 Calculate_TestVariants_Variant_Frequencies.xml --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/Calculate_TestVariants_Variant_Frequencies.xml Thu May 24 15:15:21 2012 -0400 @@ -0,0 +1,67 @@ + + + in cgatools-testvariants file + + + Calculate_TestVariants_Variant_Frequencies_0_1_0.pl + --Input $input + --First_Genome_Field_Nr $first_col + --Last_Genome_Field_Nr $last_col + --Output1 $output1 + --Output2 $output2 + + + + + + + + + + + + + + + + + + +**What it does** + +This tool calculates the allele frequencies for all variants present in the testvariant file. + +----- + +**Instructions**:: + + Calculate the frequencies of variants in a testvariants output file + Two values calculated: + Frequency vs all alleles + Frequency vs called alleles + + Input: testvariants file + Outputs: + All data to *-Freq.tsv, including scores and quals + vars and freqs to *-Freq_Short.tsv + Exceptions to *-Freq_Log + Stats to *-Freq_Stats + + + perl Calculate_TestVariants_Variant_Frequencies_0_0_3.pl \ + --Input input_file \ + --First_Genome_Field_Nr col_nr1 \ + --Last_Genome_Field_Nr col_nr2 + --Output1 output1 \ + --Output2 output_short \ + eg + perl Calculate_TestVariants_Variant_Frequencies_0_0_3.pl \ + --Input /data/Family_Quartet_testvariants.tsv \ + --Output /data/Family_Quartet_testvariants + --First_Genome_Field_Nr 9 \ + --Last_Genome_Field_Nr 11 + --Output1 /data/Family_Quartet_testvariants + --Output2 /data/Family_Quartet_testvariants_short + + +