<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Andrew Kjar</submitter><organism>Homo sapiens</organism><software>Rsubread (2.18.0)</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16510</full_dataset_link><description>Developing and benchmarking model systems to understand neurodegeneration remains an important challenge. In this work, we overexpressed mutant MAPT (P301L,V337M) in neural organoids to understand the resulting pathology.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - NGS sequencing was performed via paired-end 150 bp on an Illumina NovaSeq X Plus with a targeted 50 million reads per sample.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA samples were extracted using the QIAGEN RNeasy micro plus kit.</sample_protocol><sample_protocol>Library Construction - Purified RNA samples were submitted to the Vanderbilt Technologies for Advanced Genomics (VANTAGE) core for bulk sequencing. cDNA libraries were prepared with a stranded mRNA (polyA-selected) library preparation kit.</sample_protocol><sample_protocol>Sample Collection - Day 90 organoids were collected from culture media, washed in PBS, and then homogenized in RLT buffer with BME.</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 - Paired-end bulk RNA-seq reads were obtained as gzipped FASTQ files.  Reads were aligned to the human reference genome (hg38) using an RNA-seq–specific alignment mode with paired-end information enabled (Rsubread). Aligned BAM files were collected and quantified at the gene level using the featureCounts function. Raw counts were uploaded as the processed file.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>N/A</instrument_platform><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Andrew Kjar</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bulk RNA sequencing of mutant MAPT over-expression in neural organoids</name><description>Developing and benchmarking model systems to understand neurodegeneration remains an important challenge. In this work, we overexpressed mutant MAPT (P301L,V337M) in neural organoids to understand the resulting pathology.</description><dates><release>2026-03-31T00:00:00Z</release><modification>2026-03-31T01:03:46.789Z</modification><creation>2026-01-02T16:00:28.544Z</creation></dates><accession>E-MTAB-16510</accession><cross_references><ENA>ERP187229</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>