<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Kanishk Asthana</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15946</full_dataset_link><description>Time-Tags were injected in reverse order to help detect any time-tag specific biases. Data was also used for comparison with 10X Genomics 3' Chromium on K562 cells</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Oligo-DT beads were used to capture mRNA from lysed Single-Cells inside droplets.</sample_protocol><sample_protocol>Growth Protocol - K562 cells grown in suspension in DMEM with 10% FBS and 1%PEN-STREP at 5%CO2 and 37C.  https://kanishkasthana.github.io/ChronoSeq/protocol_for_preparing_cells_AdditionalFiltration.html</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. https://kanishkasthana.github.io/ChronoSeq/protocol_and_software_for_running_chronoseq_device.html</sample_protocol><sample_protocol>Sequencing - Illumina NovaSeq X 10B on one lane in PE100 configuration with Custom Read 1 primer</sample_protocol><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. https://kanishkasthana.github.io/ChronoSeq/protocol_library_preparation_for_dropseq_chronoseq_beads.html</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. https://github.com/kanishkasthana/ChronoSeq-Tools</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><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 Single-cell negative control with no stimulation. 12 samples were taken with ChronoSeq and barcodes with unique time-tags. Time-Tags injected from 12->1</name><description>Time-Tags were injected in reverse order to help detect any time-tag specific biases. Data was also used for comparison with 10X Genomics 3' Chromium on K562 cells</description><dates><release>2025-11-01T00:00:00Z</release><modification>2026-04-16T21:09:40.416Z</modification><creation>2025-11-01T15:26:05.466Z</creation></dates><accession>E-MTAB-15946</accession><cross_references><ENA>ERP183493</ENA><Biostudies>E-MTAB-15927</Biostudies><Biostudies>E-MTAB-15928</Biostudies><Biostudies>E-MTAB-15894</Biostudies><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></cross_references></HashMap>