ExperimentID 1275

神经鞘瘤

GSE178687

genotype: Neurotypical Contro

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Disease: 1Experiment: 1Links: 1
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Record Fields

Scalar fields from the final experiment record.

Experiment Id
1275
Evidence Id
24570
Core Evidence Id
24570
Source Experiment Id
1268
Herb2 Experiment Id
HBEXP001272
Subject Disease Key
HBDIS002458_GSE178687
Subject Disease Name
Prader-Willi Syndrome
Organism
Homo sapiens
Experiment Type
Expression profiling by high throughput sequencing
Sequence Type
total RNA
Experiment Subject
human cellline
Experiment Detail
Special Pretreatment
Control Condition
genotype: Neurotypical Contro
Control Samples
GSM5396105;GSM5396106;GSM5396107;GSM5396108
Experiment Subject Detail
Treatment Samples
GSM5396117;GSM5396118;GSM5396119;GSM5396120
Drug Delivery
Data Type
High-throughput sequencing
Data Process Pipeline
Raw data using FeatureCounts
Platform
GPL24676
Exp Number
EXP3
Strain
Tissue
Cell Type
Cell Line
Gse Id
GSE178687
Original Id
Subject Disease Name Cn
神经鞘瘤
Subject Disease Name En
Neurilemmoma
Bilingual Status
complete