<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Kanishk Asthana</submitter><organism>Homo sapiens</organism><software>ChronoSeq-Tools</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15894</full_dataset_link><description>Both Live-cell imaging studies and scRNA-seq studies have shown multiple heterogeneous responses to the same stimulus in the same cells. Therefore as a first application we investigated if ChronoSeq could also reveal the heterogeneity in stimulus response; we applied ChronoSeq to profile inflammatory responses in K562 cells stimulated with TNF-α, to capture the rapid NF-κB signaling cascade. 10 minute interval between samples including a 1 minute sampling duration.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - ChronoSeq library preparation protocol is very similar to Drop-seq. Beads from all time-tags are pooled together, then split into four equal parts for Reverse Transcription followed by PCR amplification.</sample_protocol><sample_protocol>Sequencing - Illumina NovaSeq X 10B on one lane in PE100 configuration with Custom Read 1 primer</sample_protocol><sample_protocol>Sample Collection - Automated cell sampling using ChronoSeq device. Each cell sample is injected with a unique injection of Time-Tagged ChronoSeq beads.</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 - hg38 alignment. Data processed using ChronoSeq-Tools pipeline.</data_protocol><data_protocol>Data Transformation - UMIs and gene information were used to generate unique transcripts captured and remove PCR duplicates using Drop-seq tools.</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>Illumina NovaSeq X</instrument_platform><instrument_platform>ChronoSeq</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_authors>Kanishk Asthana</pubmed_authors></additional><is_claimable>false</is_claimable><name>K562 cells treated with 10ng/ml TNFα, profiled with ChronoSeq for 12 samples barcoded with unique Time-Tags</name><description>Both Live-cell imaging studies and scRNA-seq studies have shown multiple heterogeneous responses to the same stimulus in the same cells. Therefore as a first application we investigated if ChronoSeq could also reveal the heterogeneity in stimulus response; we applied ChronoSeq to profile inflammatory responses in K562 cells stimulated with TNF-α, to capture the rapid NF-κB signaling cascade. 10 minute interval between samples including a 1 minute sampling duration.</description><dates><release>2025-11-01T00:00:00Z</release><modification>2026-05-26T13:06:43.947Z</modification><creation>2025-10-29T06:15:13.916Z</creation></dates><accession>E-MTAB-15894</accession><cross_references><ENA>ERP183239</ENA><EFO>EFO_0004170</EFO><EFO>EFO_0005684</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>