{"id":38558,"date":"2026-01-16T01:26:32","date_gmt":"2026-01-16T09:26:32","guid":{"rendered":"https:\/\/www.novogene.com\/eu-en\/?page_id=38558"},"modified":"2026-01-19T21:57:16","modified_gmt":"2026-01-20T05:57:16","slug":"single-cell-rna-sequencing","status":"publish","type":"page","link":"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/single-cell-rna-sequencing\/","title":{"rendered":"Single Cell RNA Sequencing\u00a0"},"content":{"rendered":"<p>Single-cell RNA sequencing (scRNA-seq) takes transcriptomics analysis a step further,\u00a0providing\u00a0unprecedented insights into the individual cellular heterogeneity within a population of\u00a0seemingly identical\u00a0cells in complex biological systems. This modern transcriptomics technology builds upon the foundations of bulk RNA-seq\u00a0by incorporating microfluidics or other single-cell isolation techniques to keep track of RNA from individual cells. Generally speaking,\u00a0scRNA-seq\u00a0captures the mRNA from individual cells, converts it into complementary DNA (cDNA), and constructs barcoded libraries for high-throughput sequencing. By examining gene expression at the cellular level,\u00a0scRNA-seq\u00a0enables the identification of\u00a0<strong>rare cell types<\/strong>, elucidates cellular states, enhances the\u00a0<strong>understanding of disease progression<\/strong>\u00a0and mechanisms, and\u00a0identifies\u00a0<strong>developmental\u00a0trajectories<\/strong>, among others.\u00a0<\/p>\n<p style=\"margin-top:15px;\">Importantly,\u00a0scRNA-seq\u00a0has become a powerful tool for\u00a0<strong>immune profiling at the single-cell level<\/strong>, allowing detailed characterization of immune cell populations, activation states, and functional diversity, as well as the analysis of immune receptor repertoires and cell\u2013cell interactions. These capabilities significantly enhance the understanding of immune responses in health and disease, including cancer, infection, autoimmunity, and inflammatory disorders.\u00a0<\/p>\n<p>Empower your single cell omics research with\u00a0Novogene\u2019s\u00a0end-to-end workflow powered by 10X Genomics\u2019 GEM-X technology.<\/p>\n<style>\np strong{font-family: 'Merriweather-Bold', Arial !important;}\n<\/style>\n","protected":false},"excerpt":{"rendered":"<p>Single-cell RNA sequencing (scRNA-seq) takes transcriptomics analysis a step further,\u00a0providing\u00a0unprecedented insights into the individual cellular heterogeneity within a population of\u00a0seemingly identical\u00a0cells in complex biological systems. This modern transcriptomics technology builds upon the foundations of bulk RNA-seq\u00a0by incorporating microfluidics or other single-cell isolation techniques to keep track of RNA from individual cells. Generally speaking,\u00a0scRNA-seq\u00a0captures the mRNA<\/p>\n","protected":false},"author":14,"featured_media":0,"parent":1417,"menu_order":141,"comment_status":"closed","ping_status":"closed","template":"templates\/category-page-new.php","meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v20.8 (Yoast SEO v20.8) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Single Cell RNA Sequencing\u00a0 - Novogene<\/title>\n<meta name=\"description\" content=\"Novogene provides a range of epigenomic sequencing services to suit your needs. Our services include \u2013 whole-genome methylation sequencing (whole genome bisulfite sequencing as well as enzymatic methyl sequencing) and reduced representation bisulfite sequencing (RRBS) for the precise analysis of methylated cytosines. Additionally, we can also offer methylation detection by long read sequencing platforms from PacBio and ONT. We provide chromatin immunoprecipitation sequencing (ChIP-seq) and RNA immunoprecipitation sequencing (RIP-seq) services that enable researchers to analyze protein-DNA and protein-RNA interactions, respectively, providing insight into binding motifs and the regulatory roles of nucleic acid binding proteins. Lastly, we also sequence premade libraries to support ATAC-seq projects (both bulk and single-cell).\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/single-cell-rna-sequencing\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Single Cell RNA Sequencing\u00a0\" \/>\n<meta property=\"og:description\" content=\"Novogene provides a range of epigenomic sequencing services to suit your needs. Our services include \u2013 whole-genome methylation sequencing (whole genome bisulfite sequencing as well as enzymatic methyl sequencing) and reduced representation bisulfite sequencing (RRBS) for the precise analysis of methylated cytosines. Additionally, we can also offer methylation detection by long read sequencing platforms from PacBio and ONT. We provide chromatin immunoprecipitation sequencing (ChIP-seq) and RNA immunoprecipitation sequencing (RIP-seq) services that enable researchers to analyze protein-DNA and protein-RNA interactions, respectively, providing insight into binding motifs and the regulatory roles of nucleic acid binding proteins. 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Our services include \u2013 whole-genome methylation sequencing (whole genome bisulfite sequencing as well as enzymatic methyl sequencing) and reduced representation bisulfite sequencing (RRBS) for the precise analysis of methylated cytosines. Additionally, we can also offer methylation detection by long read sequencing platforms from PacBio and ONT. We provide chromatin immunoprecipitation sequencing (ChIP-seq) and RNA immunoprecipitation sequencing (RIP-seq) services that enable researchers to analyze protein-DNA and protein-RNA interactions, respectively, providing insight into binding motifs and the regulatory roles of nucleic acid binding proteins. 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