<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Remya Bhaskaran S</submitter><study_type>transcription profiling by RT-PCR</study_type><organism>Homo sapiens</organism><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15757</full_dataset_link><description>This study evaluated the expression of depression-associated genes (GAR1, PER3, MTPAP, SLC25A26, CD19) in whole-blood samples from 100 patients with depression and 100 healthy controls using SYBR Green-based quantitative RT-PCR on the Rotor-Gene Q system.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Scaning - qRT-PCR was performed using SYBR Green chemistry on the Rotor-Gene Q system (Qiagen). β-actin was used as an endogenous control.</sample_protocol><sample_protocol>Growth Protocol - Relative expression was calculated using the 2^-ΔCt method normalized to β-actin.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was isolated using TRIzol reagent (Thermo Fisher Scientific) following the manufacturer’s protocol.</sample_protocol><sample_protocol>Labeling - cDNA was synthesized from 1 µg of total RNA using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems).</sample_protocol><sample_protocol>Hybridization - qRT-PCR was performed using SYBR Green chemistry on the Rotor-Gene Q system (Qiagen). β-actin was used as an endogenous control.</sample_protocol><sample_protocol>Sample Treatment - Relative expression was calculated using the 2^-ΔCt method normalized to β-actin.</sample_protocol><sample_protocol>Sample Collection - Whole blood samples (5 mL) were collected in EDTA tubes from patients with depression and healthy controls following informed consent.</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><pubmed_authors>Remya Bhaskaran S</pubmed_authors><data_protocol>Data Transformation - Relative expression was calculated using the 2^-ΔCt method normalized to β-actin.</data_protocol></additional><is_claimable>false</is_claimable><name>Transcription profiling by RT-PCR of GAR1, PER3, MTPAP, SLC25A26, and CD19 in depression and control blood samples</name><description>This study evaluated the expression of depression-associated genes (GAR1, PER3, MTPAP, SLC25A26, CD19) in whole-blood samples from 100 patients with depression and 100 healthy controls using SYBR Green-based quantitative RT-PCR on the Rotor-Gene Q system.</description><dates><release>2025-11-03T00:00:00Z</release><modification>2026-06-16T12:01:10.026Z</modification><creation>2025-10-16T12:27:49.588Z</creation></dates><accession>E-MTAB-15757</accession><cross_references><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>