Changes between Version 40 and Version 41 of se.lu.onk.IlluminaSNPNormalization
- Timestamp:
- Oct 17, 2008, 4:29:31 PM (16 years ago)
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se.lu.onk.IlluminaSNPNormalization
v40 v41 47 47 ### 48 48 # Windows 49 # Note that we are using ''Rscript'', which is a part of the R distribution.49 # Note that we are using Rscript, which is a part of the R distribution. 50 50 my $R_windows=File::Spec->canonpath('C:/"Program Files"/R/R-2.7.0/bin/Rscript'); 51 51 my $R_command="$R_windows --vanilla tQN.R"; … … 60 60 ||...||...||...||...||...||...||...||...||...||...|| 61 61 62 The data extracted from !BeadStudio needs to be split into a separate file for each sample using the script ''split_ beadstudio_samples.pl''.62 The data extracted from !BeadStudio needs to be split into a separate file for each sample using the script ''split_samples.pl''. 63 63 64 64 {{{ 65 perl split_ beadstudio_samples.pl --beadstudio_file=example/example_beadstudio_data.txt65 perl split_samples.pl --data_file=example/example_beadstudio_data.txt 66 66 }}} 67 67 where ''example_beadstudio_data.txt'' is a file exported from !BeadStudio in the format described above. … … 77 77 }}} 78 78 79 This command will perform tQN on the samples in the tQN subdirectory ''extracted'' that are specified in the file ''sample_names.txt''. If you want to perform tQN on a subset of samples you can edit ''sample_names.txt'' accordingly. The normalized data is stored in the tQN subdirectory ''normalized''. For each sample, there is a file with tQN normalized data. A file ''tQN_beadstudio.txt'' is also generated with tQN B allele frequencies and Log R ratios for all samples in a format suitable for import into !BeadStudio using its import sub-column process. tQN also supports generating tQN data for further analysis with PennCNV and QuantiSNP. Running tQN with the following command:79 This command will perform tQN on the samples in the tQN subdirectory ''extracted'' that are specified in the file ''sample_names.txt''. If you want to perform tQN on a subset of samples you can edit ''sample_names.txt'' accordingly. The normalized data is stored in the tQN subdirectory ''normalized''. For each sample, there is a file with tQN normalized data. A file ''tQN_beadstudio.txt'' is also generated with tQN B allele frequencies and Log R ratios for all samples in a format suitable for import into !BeadStudio using its import sub-column process. tQN also supports generating tQN data for further analysis with PennCNV, QuantiSNP and BAFsegmentation. Running tQN with the following command: 80 80 81 81 {{{ … … 83 83 }}} 84 84 85 generates one data file per sample in the tQN subdirectory ''normalized'' for further analysis using PennCNV. Alternatives for ''--output_format'' are ''QuantiSNP'', which generates one data file per sample for further analysis with QuantiSNP and ''!BeadStudio'', which is the default argument generating the default ''tQN_beadstudio.txt'' file with data for all samples. Beadchip types for which there is a cluster file in the tQN subdirectory ''lib'' are supported by tQN and can be used as alternatives for ''--beadchip''. For PennCNV and QuantiSNP, SNPs having missing values in either B allele frequencies or log R ratios after normalization are excluded from the respective output files.85 generates one data file per sample in the tQN subdirectory ''normalized'' for further analysis using PennCNV. Alternatives for ''--output_format'' are ''QuantiSNP'', which generates one data file per sample for further analysis with QuantiSNP, ''BAFsegmentation'', which generates files for further analysis with BAFsegmentation, and ''!BeadStudio'', which is the default argument generating the default ''tQN_beadstudio.txt'' file with data for all samples. Beadchip types for which there is a cluster file in the tQN subdirectory ''lib'' are supported by tQN and can be used as alternatives for ''--beadchip''. For PennCNV and QuantiSNP, SNPs having missing values in either B allele frequencies or log R ratios after normalization are excluded from the respective output files. 86 86 87 87