{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000714","ANALYSIS_ID":"AN001117","VERSION":"1","CREATED_ON":"July 2, 2017, 12:58 pm"},

"PROJECT":{"PROJECT_TITLE":"Young adult glioblastoma","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"Effect of genetic lesions on glioblastoma","INSTITUTE":"University of Michigan","DEPARTMENT":"Neurosurgery","LABORATORY":"Castro Lab","LAST_NAME":"Castro","FIRST_NAME":"Maria","ADDRESS":"Ann Arbor, MI","EMAIL":"mariacas@umich.edu","PHONE":"734-764-0850"},

"STUDY":{"STUDY_TITLE":"Effect of genetic lesions on glioblastoma (NP, NPA, NPAI, NS)","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"The cells in this experiment are primary cells derived from tumors with various genetic lesions. The purpose of this experiment is to determine the effect of the genetic lesion IDH1m (mutant isocitrate dehydrogenase) on the metabolic state of the cell. Four replicates of NPA versus four replicates of NPAI suspension cell neurospheres will be compared in an untargeted manner to identify all possible metabolic differences between the two types of genetic lesions.","INSTITUTE":"University of Michigan","DEPARTMENT":"Biomedical Research Core Facilities","LABORATORY":"Metabolomics core","LAST_NAME":"Kachman","FIRST_NAME":"Maureen","ADDRESS":"6300 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105-5714","EMAIL":"mkachman@med.umich.edu","PHONE":"(734) 232-8175","NUM_GROUPS":"2","TOTAL_SUBJECTS":"1"},

"SUBJECT":{"SUBJECT_TYPE":"Mouse","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"SU0014782",
"Sample ID":"S00022549",
"Factors":{"IDh1 mutation":"NPA"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022550",
"Factors":{"IDh1 mutation":"NPA"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022551",
"Factors":{"IDh1 mutation":"NPA"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022552",
"Factors":{"IDh1 mutation":"NPA"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022553",
"Factors":{"IDh1 mutation":"NPAI"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022554",
"Factors":{"IDh1 mutation":"NPAI"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022555",
"Factors":{"IDh1 mutation":"NPAI"}
},
{
"Subject ID":"SU0014782",
"Sample ID":"S00022556",
"Factors":{"IDh1 mutation":"NPAI"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"-"},

"TREATMENT":{"TREATMENT_SUMMARY":"-"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"-","SAMPLEPREP_PROTOCOL_FILENAME":"A003 - Untargeted Metabolomics.pdf"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Agilent","COLUMN_NAME":"Waters Acquity HSS T3 (50 x 2.1mm, 1.8um)"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","ANALYSIS_PROTOCOL_FILE":"A003 - Untargeted Metabolomics.pdf"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"Agilent 6530 QTOF","INSTRUMENT_TYPE":"QTOF","MS_TYPE":"ESI","ION_MODE":"NEGATIVE"},

"MS_METABOLITE_DATA":{
"Units":"peak area",

"Data":[{"Metabolite":"16:0-18:0 PC (M+CL)-","S00022549":"85426","S00022550":"","S00022551":"80852","S00022552":"129537","S00022553":"","S00022554":"269142","S00022555":"","S00022556":"306458"},{"Metabolite":"18:0 LYSO-PE (M-H)-","S00022549":"93169","S00022550":"135479","S00022551":"74752","S00022552":"56688","S00022553":"26297","S00022554":"20933","S00022555":"63419","S00022556":"54138"},{"Metabolite":"2-DEOXY-D-GLUCOSE (M+CL)-","S00022549":"4713","S00022550":"","S00022551":"","S00022552":"4025","S00022553":"","S00022554":"","S00022555":"206467","S00022556":""},{"Metabolite":"2-HYDROXY-3-METHYLBUTYRIC ACID (M-H)-","S00022549":"11983","S00022550":"18147","S00022551":"9672","S00022552":"12479","S00022553":"","S00022554":"","S00022555":"","S00022556":""},{"Metabolite":"2-METHYLMALEIC ACID (M-H)-","S00022549":"19281","S00022550":"16816","S00022551":"19892","S00022552":"18157","S00022553":"","S00022554":"22927","S00022555":"15172","S00022556":""},{"Metabolite":"3-(4-HYDROXYPHENYL)LACTIC 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}