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define models for imported instrument data.
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#List all the instrument-data that is imported | |
genome instrument-data list imported "sample.patient.common_name='TST1ds' and sample.extraction_type = 'genomic dna'" | |
genome instrument-data list imported "sample.patient.common_name='TST1ds' and sample.extraction_type = 'rna'" | |
#Define the models based on imported instrument-data, rename the ID's | |
genome model define rna-seq --reference-sequence-build='106942997' --annotation-build='124434505' --cancer-annotation-db='tgi/cancer-annotation/human/build37-20131010.1' --subject='H_NJ-HCC1395ds-HCC1395_RNA' --processing-profile='2762841' --instrument-data='0296e0aeeb3f4daab1e8604cddb2cb70' --model-name='hcc1395ds-tumor-rnaseq' | |
genome model define rna-seq --reference-sequence-build='106942997' --annotation-build='124434505' --cancer-annotation-db='tgi/cancer-annotation/human/build37-20131010.1' --subject='H_NJ-HCC1395ds-HCC1395_BL_RNA' --processing-profile='2762841' --instrument-data='675561c466744c8498f903b77ee9acbe' --model-name='hcc1395ds-normal-rnaseq' | |
genome model define reference-alignment --reference-sequence-build='106942997' --annotation-reference-build='124434505' --subject='H_NJ-HCC1395ds-HCC1395' --processing-profile='2635769' --dbsnp-build='127786607' --target-region-set-names='NimbleGen v3 Capture Chip Set' --region-of-interest-set-name='NimbleGen v3 Capture Chip Set' --instrument-data='4d012edfdb154310a2e390ce3c47b26c' --model-name='hcc1395ds-tumor-refalign-exome' | |
genome model define reference-alignment --reference-sequence-build='106942997' --annotation-reference-build='124434505' --subject='H_NJ-HCC1395ds-HCC1395' --processing-profile='2635769' --dbsnp-build='127786607' --instrument-data='7bb1ff78eea545dba8b5909276d83bc1,ee9fd6cec05046248ee45b30e79ff7e8,f0e9afd3b8f84952923ceb4f761e762a,85a6d2d6d1b64d2d881c7f2558629432,a750da970d7d4f19ae5ab0e8eb18a94d' --model-name='hcc1395ds-tumor-refalign-wgs' | |
genome model define reference-alignment --reference-sequence-build='106942997' --annotation-reference-build='124434505' --subject='H_NJ-HCC1395ds-HCC1395_BL' --processing-profile='2635769' --dbsnp-build='127786607' --target-region-set-names='NimbleGen v3 Capture Chip Set' --region-of-interest-set-name='NimbleGen v3 Capture Chip Set' --instrument-data='3562f8ead8bf4a8881f773184f6f22d1' --model-name='hcc1395ds-normal-refalign-exome' | |
genome model define reference-alignment --reference-sequence-build='106942997' --annotation-reference-build='124434505' --subject='H_NJ-HCC1395ds-HCC1395_BL' --processing-profile='2635769' --dbsnp-build='127786607' --instrument-data='667e244fbb90442badfa78eebe717302,5ca9c666406544bc971108d110fa02f2,b41e2ea9d3d14fd2a063956c896b9544' --model-name='hcc1395ds-normal-refalign-wgs' | |
genome model define somatic-variation --tumor-model='hcc1395-tumor-refalign-exome' --normal-model='hcc1395-normal-refalign-exome' --processing-profile=2762563 --annotation-build=124434505 --previously-discovered-variations-build=127786607 --model-name='hcc1395ds-somatic-exome' | |
genome model define somatic-variation --tumor-model='hcc1395-tumor-refalign-wgs' --normal-model='hcc1395-normal-refalign-wgs' --processing-profile=2762563 --annotation-build=124434505 --previously-discovered-variations-build=127786607 --model-name='hcc1395ds-somatic-wgs' |
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