<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE344nnn/GSE344124/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species> synthetic construct</species><species> Homo sapiens</species><species>Drosophila melanogaster</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE344124</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Omega-seq: ultra-low-background RNA sequencing with faithful molecular counting and precise transcript-end capture</name><description>PCR-based RNA sequencing generates phantom unique molecular identifiers (UMIs) when residual UMI-bearing oligonucleotides reprime during amplification, inflating molecule counts and corrupting relative abundances; non-specific amplification limits sensitivity, and synthetic poly-T tracts disrupt sequencing and obscure transcript 3' ends. This series contains the sequencing data for Omega-seq, a full-length single-cell RNA-seq method that restricts UMI incorporation to reverse transcription using uracil-containing, USER-excisable template-switching oligonucleotides together with a uracil-intolerant polymerase, and that replaces the conventional oligo-dT primer with an Omega-shaped dT primer which relocates the sequencing adapter past the homopolymer tract. The data comprise (i) serial dilutions of human brain total RNA (10, 1 and 0.1 pg) and no-template controls processed in parallel by Omega-seq and FLASH-seq-UMI, with ERCC spike-ins, on Illumina; (ii) FACS-sorted individual Drosophila larval neuroblasts, and pooled neuroblasts and neurons, prepared by both methods; (iii) an oligonucleotide-design comparison of standard versus Omega-shaped dT primers; and (iv) a Nanopore run in which preamplified cDNA from both methods across the same dilution series was barcoded and sequenced on a single flow cell, used to characterise adapter composition and mappability of the preamplification products directly. Processed data are provided as per-library gene-by-cell UMI count matrices. The Nanopore run is deposited here as its eight demultiplexed libraries; reads for which no barcode could be recovered are not included in this Series, and are deposited with the Zenodo record accompanying the publication.</description><dates><publication>2026/08/18</publication></dates><accession>GSE344124</accession><cross_references><GSM>GSM9971081</GSM><GSM>GSM9971082</GSM><GSM>GSM9971080</GSM><GSM>GSM9971108</GSM><GSM>GSM9971109</GSM><GSM>GSM9971106</GSM><GSM>GSM9971107</GSM><GSM>GSM9971104</GSM><GSM>GSM9971105</GSM><GSM>GSM9971102</GSM><GSM>GSM9971103</GSM><GSM>GSM9971100</GSM><GSM>GSM9971089</GSM><GSM>GSM9971101</GSM><GSM>GSM9971087</GSM><GSM>GSM9971088</GSM><GSM>GSM9971085</GSM><GSM>GSM9971086</GSM><GSM>GSM9971083</GSM><GSM>GSM9971084</GSM><GSM>GSM9971092</GSM><GSM>GSM9971093</GSM><GSM>GSM9971090</GSM><GSM>GSM9971091</GSM><GSM>GSM9971115</GSM><GSM>GSM9971113</GSM><GSM>GSM9971114</GSM><GSM>GSM9971078</GSM><GSM>GSM9971111</GSM><GSM>GSM9971112</GSM><GSM>GSM9971079</GSM><GSM>GSM9971098</GSM><GSM>GSM9971077</GSM><GSM>GSM9971099</GSM><GSM>GSM9971110</GSM><GSM>GSM9971096</GSM><GSM>GSM9971097</GSM><GSM>GSM9971094</GSM><GSM>GSM9971095</GSM><GPL>34457</GPL><GPL>34698</GPL><GPL>34284</GPL><GSE>344124</GSE><taxon> synthetic construct</taxon><taxon> Homo sapiens</taxon><taxon>Drosophila melanogaster</taxon></cross_references></HashMap>