<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Domenico Palumbo</submitter><organism>Homo sapiens</organism><software>STAR</software><software>DESeq2</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15198</full_dataset_link><description>In this study, we performed the transcriptome analysis of a cohort comprising 72 (20 already published E-MTAB-11599) MTC (medullary thyroid carcinoma) specimens from patients with different genetic background (w/o RET or RAS mutations).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted from fresh-frozen tissue samples using the Norgen Kit (Biotek Corp, Ontario, Canada), following the manufacturer’s instructions.</sample_protocol><sample_protocol>Library Construction - Libraries preparation was performed by using the TruSeq Stranded Total RNA kit (Cat. 20020598, Illumina) according to manufacturer’s guidelines and starting from 200 ng of input material.</sample_protocol><sample_protocol>Sample Collection - Patients' tissues collection was performed at Padua Hospital during surgery. The samples were frozen at -80 C° before RNA extraction.</sample_protocol><sample_protocol>Sequencing - Libraries were sequenced on NextSeq 500 platform (Illumina) in paired end mode (2 × 75 bp).</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - DESeq2 package (v1.44.0) in R was employed for detection of differentially expressed genes. Genes with a sum of counts less than 10 in all the samples were removed and the data were normalized taking into account sex and batch as variables. Genes were considered differentially expressed if they showed |FC| ≥ 1.5 and adjusted p-value ≤ 0.05.</data_protocol><data_protocol>Sequence Alignment - Alignment was performed against human genome version hg38 (gencode release 37) with STAR (v2.7.11b) and expressed genes were identified using featureCounts (v2.0.1).</data_protocol><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><instrument_platform>TruSeq Stranded Total RNA kit</instrument_platform><instrument_platform>Norgen Kit (Biotek Corp)</instrument_platform><instrument_platform>NextSeq 500</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_title>Comprehensive Transcriptome Profiling of Sporadic Medullary Thyroid Carcinoma</pubmed_title><pubmed_authors>Domenico Palumbo</pubmed_authors><pubmed_authors>Domenico Palumbo, Viola Melone, Luigi Palo, Fabio Russo, Domenico Rocco, Caterina Mian, Susi Barollo, Simona Censi, Loris Bertazza, Maria Chiara Zatelli, Alessandro Weisz, Roberta Tarallo, Mario Vitale</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive Transcriptome Profiling of Sporadic Medullary Thyroid Carcinoma</name><description>In this study, we performed the transcriptome analysis of a cohort comprising 72 (20 already published E-MTAB-11599) MTC (medullary thyroid carcinoma) specimens from patients with different genetic background (w/o RET or RAS mutations).</description><dates><release>2026-01-07T00:00:00Z</release><modification>2026-01-07T10:19:39.03Z</modification><creation>2025-06-04T19:47:40.76Z</creation></dates><accession>E-MTAB-15198</accession><cross_references><ENA>ERP173171</ENA><Biostudies>E-MTAB-11599</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><doi>www.doi.org/10.1038/s41597-026-06550-7</doi></cross_references></HashMap>