<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Allison Dupzyk</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15272</full_dataset_link><description>QIC-seq combines virus-inclusive and perturb single cell RNA sequencing in order to systematically compare host factor requirements among divergent flaviviruses.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - After 48 hours of mock or infection, cells were washed, and trypsinized and resuspended in PBS and BSA to prevent clumping.</sample_protocol><sample_protocol>Sequencing - Illumina NGS on Novaseq lane. PE150. Sequencing conducted by Novogene</sample_protocol><sample_protocol>Growth Protocol - Cells were grown in complete DMEM or IMDM media supplemented with 10% FBS.</sample_protocol><sample_protocol>Sample Treatment - Cells were either mock infected or infected with virus at varying MOIs for 48 hours.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Cells were lysed, and RT-PCR was used to capture host transcriptome, viral genomes, and sgRNAs to identify perturbed cells. cDNA was size selected to generate a larger cDNA library (transcriptomic) and a smaller DNA library (viral and CRISPR) .</sample_protocol><sample_protocol>Library Construction - 10X genomics 5' VDJ protocol was followed for the transcriptomic library, READ2 was placed onto cDNA in small viral and CRISPR library by PCR before re-incorporation into the remaining protocol.</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>Sequence Alignment - 10X Genomics Cellranger was used.</data_protocol><data_protocol>Data Transformation - Data was normalized using Seurat's SCTransformation or normalize data function().</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_authors>Allison Dupzyk</pubmed_authors></additional><is_claimable>false</is_claimable><name>QIC-seq of Huh7.5.1 cells challenged with DENV, WNV, YFV, and LGTV. QIC-seq of Hap1 cells challenged with DENV and WNV</name><description>QIC-seq combines virus-inclusive and perturb single cell RNA sequencing in order to systematically compare host factor requirements among divergent flaviviruses.</description><dates><release>2026-04-17T00:00:00Z</release><modification>2026-04-17T20:38:38.167Z</modification><creation>2025-06-25T15:53:19.877Z</creation></dates><accession>E-MTAB-15272</accession><cross_references><ENA>ERP174043</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005684</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>