data preprocessing rna sequencing libraries Search Results


90
MetWare Ltd rna quantification and qualification, cdna libraries preparation, clustering and sequencing and data analyses
Rna Quantification And Qualification, Cdna Libraries Preparation, Clustering And Sequencing And Data Analyses, supplied by MetWare Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+preprocessing+rna+sequencing+libraries/pm37441529-89-11-16?v=MetWare+Ltd
Average 90 stars, based on 1 article reviews
rna quantification and qualification, cdna libraries preparation, clustering and sequencing and data analyses - by Bioz Stars, 2026-08
90/100 stars
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90
Lexogen GmbH ribosomal rna (rrna) depletion, library preparation, sequencing and initial data processing
Ribosomal Rna (Rrna) Depletion, Library Preparation, Sequencing And Initial Data Processing, supplied by Lexogen GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+preprocessing+rna+sequencing+libraries/pmc10213629-78-6-14?v=Lexogen+GmbH
Average 90 stars, based on 1 article reviews
ribosomal rna (rrna) depletion, library preparation, sequencing and initial data processing - by Bioz Stars, 2026-08
90/100 stars
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90
Arraystar inc rna-seq library preparation, sequencing and data analysis
Rna Seq Library Preparation, Sequencing And Data Analysis, supplied by Arraystar inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+preprocessing+rna+sequencing+libraries/bio_rxiv__2020__10__29__361105-61-5-10?v=Arraystar+inc
Average 90 stars, based on 1 article reviews
rna-seq library preparation, sequencing and data analysis - by Bioz Stars, 2026-08
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90
Oxford Gene Technology rna sequencing (rna-seq) analysis
Differential <t>RNA</t> expression in HSP90i-resistant clones compared to parental Hs578T cells. RNA samples from DMSO-treated and ganetespib-treated Hs578T, CR2 and CR3 cells were analysed for whole transcriptome profiling with <t>RNA-sequencing.</t> Differential gene expression analyses were performed between DMSO-treated parental Hs578T cells with either DMSO-treated CR2 or CR3 and the significantly upregulated genes observed in these clones were mostly overlapping. Pathway enrichment analysis using Metacore™ was performed on the significantly upregulated overlapping genes. The graph represents the top 20 most significantly upregulated pathways in the HSP90i-resistant clones, with FDR (false discovery rate) value < 0.05. Pathways highlighted in blue are linked to JAK-STAT signalling
Rna Sequencing (Rna Seq) Analysis, supplied by Oxford Gene Technology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+preprocessing+rna+sequencing+libraries/pmc06345040-76-11-15?v=Oxford+Gene+Technology
Average 90 stars, based on 1 article reviews
rna sequencing (rna-seq) analysis - by Bioz Stars, 2026-08
90/100 stars
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90
ChunLab Inc cdna synthesis, library construction, rna sequencing, and data processing
Differential <t>RNA</t> expression in HSP90i-resistant clones compared to parental Hs578T cells. RNA samples from DMSO-treated and ganetespib-treated Hs578T, CR2 and CR3 cells were analysed for whole transcriptome profiling with <t>RNA-sequencing.</t> Differential gene expression analyses were performed between DMSO-treated parental Hs578T cells with either DMSO-treated CR2 or CR3 and the significantly upregulated genes observed in these clones were mostly overlapping. Pathway enrichment analysis using Metacore™ was performed on the significantly upregulated overlapping genes. The graph represents the top 20 most significantly upregulated pathways in the HSP90i-resistant clones, with FDR (false discovery rate) value < 0.05. Pathways highlighted in blue are linked to JAK-STAT signalling
Cdna Synthesis, Library Construction, Rna Sequencing, And Data Processing, supplied by ChunLab Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+preprocessing+rna+sequencing+libraries/10__1096_slash_fj__201902662r-68-22-27?v=ChunLab+Inc
Average 90 stars, based on 1 article reviews
cdna synthesis, library construction, rna sequencing, and data processing - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


Differential RNA expression in HSP90i-resistant clones compared to parental Hs578T cells. RNA samples from DMSO-treated and ganetespib-treated Hs578T, CR2 and CR3 cells were analysed for whole transcriptome profiling with RNA-sequencing. Differential gene expression analyses were performed between DMSO-treated parental Hs578T cells with either DMSO-treated CR2 or CR3 and the significantly upregulated genes observed in these clones were mostly overlapping. Pathway enrichment analysis using Metacore™ was performed on the significantly upregulated overlapping genes. The graph represents the top 20 most significantly upregulated pathways in the HSP90i-resistant clones, with FDR (false discovery rate) value < 0.05. Pathways highlighted in blue are linked to JAK-STAT signalling

Journal: BMC Cancer

Article Title: Overcoming acquired resistance to HSP90 inhibition by targeting JAK-STAT signalling in triple-negative breast cancer

doi: 10.1186/s12885-019-5295-z

Figure Lengend Snippet: Differential RNA expression in HSP90i-resistant clones compared to parental Hs578T cells. RNA samples from DMSO-treated and ganetespib-treated Hs578T, CR2 and CR3 cells were analysed for whole transcriptome profiling with RNA-sequencing. Differential gene expression analyses were performed between DMSO-treated parental Hs578T cells with either DMSO-treated CR2 or CR3 and the significantly upregulated genes observed in these clones were mostly overlapping. Pathway enrichment analysis using Metacore™ was performed on the significantly upregulated overlapping genes. The graph represents the top 20 most significantly upregulated pathways in the HSP90i-resistant clones, with FDR (false discovery rate) value < 0.05. Pathways highlighted in blue are linked to JAK-STAT signalling

Article Snippet: Duplicate samples (1 μg RNA in 30 μl) were subjected to RNA Sequencing (RNA-seq) analysis (Oxford Gene Technology) and gene expression was quantified using their analysis pipeline [ ].

Techniques: RNA Expression, Clone Assay, RNA Sequencing, Gene Expression