{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000320","ANALYSIS_ID":"AN000509","VERSION":"1","CREATED_ON":"January 15, 2016, 12:53 pm"},

"PROJECT":{"PROJECT_TITLE":"Single treatment gene impact on Arabidopsis metabolites","PROJECT_SUMMARY":"This experiment aims to measure the impact of the genes that have been introduced into WT lines and compare the metabolic profiling of these plants with WT control plants. Compounds of particular intereset for this study include pyruvate, fumarate, malate, glyoxylate, anthocyanin, carotenes, and lipid compounds.","INSTITUTE":"University of California, Davis","DEPARTMENT":"Genome and Biomedical Sciences Facility","LABORATORY":"WCMC Metabolomics Core","LAST_NAME":"Fiehn","FIRST_NAME":"Oliver","ADDRESS":"1315 Genome and Biomedical Sciences Facility, 451 Health Sciences Drive, Davis, CA 95616","EMAIL":"ofiehn@ucdavis.edu","PHONE":"(530) 754-8258","FUNDING_SOURCE":"U24DK097154"},

"STUDY":{"STUDY_TITLE":"Single treatment gene impact on Arabidopsis metabolites","STUDY_SUMMARY":"This experiment aims to measure the impact of the genes that have been introduced into WT lines and compare the metabolic profiling of these plants with WT control plants. Compounds of particular intereset for this study include pyruvate, fumarate, malate, glyoxylate, anthocyanin, carotenes, and lipid compounds.","INSTITUTE":"University of California, Davis","DEPARTMENT":"Genome and Biomedical Sciences Facility","LABORATORY":"WCMC Metabolomics Core","LAST_NAME":"Fiehn","FIRST_NAME":"Oliver","ADDRESS":"1315 Genome and Biomedical Sciences Facility, 451 Health Sciences Drive, Davis, CA 95616","EMAIL":"ofiehn@ucdavis.edu","PHONE":"(530) 754-8258","NUM_GROUPS":"6","TOTAL_SUBJECTS":"34","STUDY_COMMENTS":"Andrew Burch"},

"SUBJECT":{"SUBJECT_TYPE":"Plant","SUBJECT_SPECIES":"Arabidopsis thaliana"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"Seed-Control-A",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-Control-B",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-Control-C",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-Control-D",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-Control-E",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-Control-F",
"Factors":{"Treatment":"Control"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-1A",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-1B",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-2A",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-2B",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-3A",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-111-3B",
"Factors":{"Treatment":"111"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-133-1A",
"Factors":{"Treatment":"133"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-133-1B",
"Factors":{"Treatment":"133"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-133-2A",
"Factors":{"Treatment":"133"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-133-2B",
"Factors":{"Treatment":"133"}
},
{
"Subject ID":"-",
"Sample ID":"Seed-133-3A",
"Factors":{"Treatment":"133"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"Plants are 30-35d old. They were harvested in liquid N2, grounded to fine powder, distributed to individual falcon tubes and kept at dry ice before handing over the sample to core facility.","COLLECTION_PROTOCOL_FILENAME":"StudyDesign-AvinashSrivastava-82514.pdf","SAMPLE_TYPE":"Seeds"},

"TREATMENT":{"TREATMENT_SUMMARY":"Single treatment gene impact on plant metabolites and compared to WT control: 1. Control (A,B,C,D,E,F total 6 replicates) 2. Sample 1 (A,B,C,D,E,F total 6 replicates) 3. Sample 2. (A,B,C,D,E,F total 6 replicates)","TREATMENT_PROTOCOL_FILENAME":"StudyDesign-AvinashSrivastava-82514.pdf"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"-","SAMPLEPREP_PROTOCOL_FILENAME":"Sample_Prep_Avinash_Srivastava_mx_188894.pdf"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_SUMMARY":"UPLC","CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Unspecified","COLUMN_NAME":"Waters Acquity CSH C18 (100 x 2.1mm, 1.7um) 1.7um Pre-Column","FLOW_GRADIENT":"15% B to 99% B","FLOW_RATE":"0.6 mL/min","COLUMN_TEMPERATURE":"65 C","METHODS_FILENAME":"Data Dictionary Fiehn laboratory_CSH QTOF lipidomics_05-29-2014.pdf","SOLVENT_A":"60:40 Acetonitrile:Water +10mM Ammonium Formate +10mM Formic Acid","SOLVENT_B":"9:1 Isopropanol:Acetonitrile +10mM Ammonium Formate +10mM Formic Acid","COLUMN_PRESSURE":"450-850 bar","INTERNAL_STANDARD":"See data dictionary","RETENTION_TIME":"See data dictionary","SAMPLE_INJECTION":"1.67 uL","ANALYTICAL_TIME":"13 min","CAPILLARY_VOLTAGE":"3500","TIME_PROGRAM":"15 min","WEAK_WASH_SOLVENT_NAME":"Isopropanol","WEAK_WASH_VOLUME":"5 seconds","STRONG_WASH_SOLVENT_NAME":"Isopropanol","TARGET_SAMPLE_TEMPERATURE":"Autosampler temp 4 C","RANDOMIZATION_ORDER":"Excel"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","LABORATORY_NAME":"WCMC Metabolomics Core","DETECTOR_TYPE":"TOF MCP","SOFTWARE_VERSION":"MassHunter","DATA_FORMAT":".d"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"Agilent 6550 QTOF","INSTRUMENT_TYPE":"QTOF","MS_TYPE":"ESI","ION_MODE":"NEGATIVE","CAPILLARY_VOLTAGE":"3500","COLLISION_GAS":"Nitrogen","DRY_GAS_FLOW":"8 l/min","DRY_GAS_TEMP":"325","FRAGMENT_VOLTAGE":"120","FRAGMENTATION_METHOD":"Auto MS/MS","ION_SOURCE_TEMPERATURE":"325","ION_SPRAY_VOLTAGE":"1000","IONIZATION":"Pos","PRECURSOR_TYPE":"Intact Molecule","REAGENT_GAS":"Nitrogen","SOURCE_TEMPERATURE":"325 C","DESOLVATION_GAS_FLOW":"11 l/min","DESOLVATION_TEMPERATURE":"350 C","NEBULIZER":"35 psig","OCTPOLE_VOLTAGE":"750","RESOLUTION_SETTING":"Extended Dynamic Range","SCAN_RANGE_MOVERZ":"60-1700 Da","SCANNING_CYCLE":"2 Hz","SCANNING_RANGE":"60-1700 Da","SKIMMER_VOLTAGE":"65"},

"MS_METABOLITE_DATA":{
"Units":"Peak height",

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