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comprehensive whole transcriptome sequencing  (Novogene)

 
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    Novogene comprehensive whole transcriptome sequencing
    Comprehensive Whole Transcriptome Sequencing, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/whole+transcriptome+sequencing/sequencing+transcriptome/pm41829040-91-6-0
    Average 86 stars, based on 1 article reviews
    comprehensive whole transcriptome sequencing - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Sequencing:

    Article Title: An astragalus polysaccharide-loaded hydrogel dressing enhances diabetic wound healing via dual-mode electrical stimulation
    Article Snippet: .. The transcriptomic sequencing was performed by the platform of Novogene Co., Ltd, including library construction, high-throughput sequencing, and subsequent analysis (i.e., Differential gene expression analysis, Gene Ontology enrichment analysis, and Gene Set Enrichment Analysis). ..

    Article Title: A Substrate-Dependent Bifunctional Dioxygenase from Fraxinus chinensis for O -Demethylation and C8-Hydroxylation of Coumarins.
    Article Snippet: .. Transcriptome sequencing and bioinformatic analyses were performed by Novogene Co., Ltd. (Beijing, China). .. Restriction enzymes NdeI and HindIII were obtained from New England Biolabs (Ipswich, MA, USA).

    Article Title: Integrative whole-transcriptome analysis of circRNAs, lncRNAs, miRNAs, and mRNAs reveals regulatory networks in mouse brain during Toxoplasma gondii infection.
    Article Snippet: .. We thank Novogene Co., Ltd., China. for technical assistance in Whole transcriptome sequencing. ..

    Article Title: Genome-wide characterisation of the myosin light chain gene family in Chinese perch (Siniperca chuatsi) and its expression patterns in muscle fibre types and injury response.
    Article Snippet: The Class II myosin light chain (myl) genes in Chinese perch (Siniperca chuatsi) have not yet been systematically characterised, and relationships with muscle fibre specification, development, and injury-associated remodelling remain unclear.. In this study, fast and slow muscle fibres were initially distinguished using myofibrillar ATPase histochemistry.. Subsequently, genome-wide mining identified 16 Class II myl genes, comprising eight essential and eight regulatory light-chain subunits.

    Article Title: Designer Dynamic DNA Nanoaggregate in Living Cell for Mitochondrial Energy Restriction.
    Article Snippet: .. The qualified RNA samples were then sent to Novogene Biotech Co., Ltd. (Beijing, China) for transcriptome sequencing. ..

    Next-Generation Sequencing:

    Article Title: An astragalus polysaccharide-loaded hydrogel dressing enhances diabetic wound healing via dual-mode electrical stimulation
    Article Snippet: .. The transcriptomic sequencing was performed by the platform of Novogene Co., Ltd, including library construction, high-throughput sequencing, and subsequent analysis (i.e., Differential gene expression analysis, Gene Ontology enrichment analysis, and Gene Set Enrichment Analysis). ..

    Gene Expression:

    Article Title: An astragalus polysaccharide-loaded hydrogel dressing enhances diabetic wound healing via dual-mode electrical stimulation
    Article Snippet: .. The transcriptomic sequencing was performed by the platform of Novogene Co., Ltd, including library construction, high-throughput sequencing, and subsequent analysis (i.e., Differential gene expression analysis, Gene Ontology enrichment analysis, and Gene Set Enrichment Analysis). ..



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    Image Search Results


    Transcriptomic profiling of the pretreatment biopsy sample. RNA-seq was used to obtain gene expression profiles of tumor samples. A global embedding of cancer types was calculated by transforming these gene expression profiles using PCA, followed by a t-SNE transformation to obtain a 2-dimensional approximate “map” of transcriptional similarity. The new patient sample is projected onto a pre-calculated PCA embedding space based on historical samples analyzed at Caris. Its proximity to other samples on the map reflects shared transcriptional programs with these samples. Only the immediate neighborhoods of samples should be considered for further interpretation since t-SNE embeddings do not preserve similarity correlations over long distances. Each point on the t-SNE map represents a different sample. The target symbol represents the present patient’s pretreatment biopsy sample. PCA, principal component analysis; t-SNE, t-stochastic neighbor embedding.

    Journal: Therapeutic Advances in Medical Oncology

    Article Title: Lineage infidelity in FH-deficient RCC with secondary somatic alterations: a case report and implications for diagnosis and treatment

    doi: 10.1177/17588359261456676

    Figure Lengend Snippet: Transcriptomic profiling of the pretreatment biopsy sample. RNA-seq was used to obtain gene expression profiles of tumor samples. A global embedding of cancer types was calculated by transforming these gene expression profiles using PCA, followed by a t-SNE transformation to obtain a 2-dimensional approximate “map” of transcriptional similarity. The new patient sample is projected onto a pre-calculated PCA embedding space based on historical samples analyzed at Caris. Its proximity to other samples on the map reflects shared transcriptional programs with these samples. Only the immediate neighborhoods of samples should be considered for further interpretation since t-SNE embeddings do not preserve similarity correlations over long distances. Each point on the t-SNE map represents a different sample. The target symbol represents the present patient’s pretreatment biopsy sample. PCA, principal component analysis; t-SNE, t-stochastic neighbor embedding.

    Article Snippet: To confirm the diagnosis, molecular testing (next-generation sequencing (NGS); whole exome and whole transcriptome sequencing, Caris Life Sciences (Irving, Texas, United States)) revealed an S419P mutation in the FH gene, along with pathogenic mutations in KMT2A , NF2 , and TP53 , discussed in greater detail below.

    Techniques: RNA Sequencing, Gene Expression, Transformation Assay