Review




Structured Review

Novogene sequencing libraries
Sequencing Libraries, 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/sequencing+library/libraries+sequencing/pmc13156682-346-0-11
Average 86 stars, based on 1 article reviews
sequencing libraries - by Bioz Stars, 2026-09
86/100 stars

Images

Related Articles

Sequencing:

Article Title: Characterization and Phylogenetic Analysis of the Complete Mitogenomes of Valsa mali and Valsa pyri .
Article Snippet: The quality of the harvested DNA was qualitatively evaluated by agarose gel electrophoresis and quantified on the Qubit 2.0 fluorometer system (Thermo Scientific, Waltham, MA, USA). .. High-quality DNA was sent to the Novogene Company (Cambridge, UK), where the 350 bp sequencing library was constructed for short-read Illumina sequencing, and another 10K sequencing library was also constructed for long-read Nanopore sequencing. .. The whole-genome sequencing was performed on the Illumina NovaSeq PE150 and Nanopore PromethION platforms (Illumina, San Diego, CA, USA).

Article Title: Comparative analysis of the seed microbiome in four major oilseed crops (rapeseed, sunflower, soybean, sesame) reveals host-specific assembly and potential application of seed core microbes
Article Snippet: .. Finally, the PCR products was mixed and the sequencing library was sent to the Company (Novogene, China). ..

Article Title: PRMT5 encourages cell migration and metastasis of tongue squamous cell carcinoma through methylating ΔNp63α.
Article Snippet: Tongue squamous cell carcinoma (TSCC) is a common oral malignancy prone to metastasis, whose underlying mechanism remains obscure.. Here, we report the oncogenic roles of protein arginine methyltransferase 5 (PRMT5) in TSCC via inhibiting transcription factor ΔNp63α.. We found that PRMT5 physically interacts with ΔNp63α, resulting in impairment of ΔNp63α-mediated transcriptional regulation.

Article Title: Distinct ossification trade-offs illuminate the shoulder girdle reconfiguration at the water-to-land transition.
Article Snippet: .. The RNA samples were submitted to Novogene (CA, USA), converted to sequencing library, and sequenced. ..

Article Title: CEBPB-high dormant tumor cells drive immune evasion via S100A8 orchestrated tumor-associated macrophages reprogramming
Article Snippet: For ChIP-seq, the DNA purity of input and IP- CEBPB in 4T07 cells was checked using the NanoPhotometer® spectrophotometer (IMPLEN). .. A sequencing library was then constructed by Novogene Corporation. .. Paired-end sequencing (150 bp) was subsequently performed on Illumina platform (Illumina).

Article Title: Long Non-Coding RNA RAB11B-AS1 Suppresses Cervical Cancer Progression by Upregulating RPL26 Expression
Article Snippet: .. Construction of the sequencing library and RNA-sequencing (RNA-seq) were performed by Beijing Novogene Company. ..

Article Title: The E3 ligase TRIM21 promotes progression of pancreatic ductal adenocarcinoma by down-regulating TAp63α and derepressing IL20RB .
Article Snippet: Pancreatic ductal adenocarcinoma (PDAC) is an aggressive tumor and frequently has mutations in the transcription factor p53.. TAp63α is a member of the p53 protein family that is generally tumor suppressive in various other p53mutant or p53deficient cancers.. Here, we found that TAp63α inhibited cell proliferation, epithelialmesenchymal transition (EMT), and migration in several p53mutant PDAC cell lines.

Article Title: A new dietary rat model fully recapitulates metabolic dysfunction-associated steatotic liver disease pathophysiology and mimics human disease with advanced liver fibrosis and portal hypertension
Article Snippet: Brie y, 20 mg of liver tissue was weighed and RNA was isolated using the miRNeasy Mini Kit (217004; Qiagen, Hilden, Germany) following the manufacturer’s instructions. .. The sequencing library was prepared by Novogene Co., Ltd. (Cambridge, UK) using 1000 ng of total RNA. ..

Construct:

Article Title: Characterization and Phylogenetic Analysis of the Complete Mitogenomes of Valsa mali and Valsa pyri .
Article Snippet: The quality of the harvested DNA was qualitatively evaluated by agarose gel electrophoresis and quantified on the Qubit 2.0 fluorometer system (Thermo Scientific, Waltham, MA, USA). .. High-quality DNA was sent to the Novogene Company (Cambridge, UK), where the 350 bp sequencing library was constructed for short-read Illumina sequencing, and another 10K sequencing library was also constructed for long-read Nanopore sequencing. .. The whole-genome sequencing was performed on the Illumina NovaSeq PE150 and Nanopore PromethION platforms (Illumina, San Diego, CA, USA).

Article Title: CEBPB-high dormant tumor cells drive immune evasion via S100A8 orchestrated tumor-associated macrophages reprogramming
Article Snippet: For ChIP-seq, the DNA purity of input and IP- CEBPB in 4T07 cells was checked using the NanoPhotometer® spectrophotometer (IMPLEN). .. A sequencing library was then constructed by Novogene Corporation. .. Paired-end sequencing (150 bp) was subsequently performed on Illumina platform (Illumina).

Nanopore Sequencing:

Article Title: Characterization and Phylogenetic Analysis of the Complete Mitogenomes of Valsa mali and Valsa pyri .
Article Snippet: The quality of the harvested DNA was qualitatively evaluated by agarose gel electrophoresis and quantified on the Qubit 2.0 fluorometer system (Thermo Scientific, Waltham, MA, USA). .. High-quality DNA was sent to the Novogene Company (Cambridge, UK), where the 350 bp sequencing library was constructed for short-read Illumina sequencing, and another 10K sequencing library was also constructed for long-read Nanopore sequencing. .. The whole-genome sequencing was performed on the Illumina NovaSeq PE150 and Nanopore PromethION platforms (Illumina, San Diego, CA, USA).

Polymerase Chain Reaction:

Article Title: Comparative analysis of the seed microbiome in four major oilseed crops (rapeseed, sunflower, soybean, sesame) reveals host-specific assembly and potential application of seed core microbes
Article Snippet: .. Finally, the PCR products was mixed and the sequencing library was sent to the Company (Novogene, China). ..

Reverse Transcription:

Article Title: PRMT5 encourages cell migration and metastasis of tongue squamous cell carcinoma through methylating ΔNp63α.
Article Snippet: Tongue squamous cell carcinoma (TSCC) is a common oral malignancy prone to metastasis, whose underlying mechanism remains obscure.. Here, we report the oncogenic roles of protein arginine methyltransferase 5 (PRMT5) in TSCC via inhibiting transcription factor ΔNp63α.. We found that PRMT5 physically interacts with ΔNp63α, resulting in impairment of ΔNp63α-mediated transcriptional regulation.

RNA sequencing:

Article Title: Long Non-Coding RNA RAB11B-AS1 Suppresses Cervical Cancer Progression by Upregulating RPL26 Expression
Article Snippet: .. Construction of the sequencing library and RNA-sequencing (RNA-seq) were performed by Beijing Novogene Company. ..

RNA Sequencing:

Article Title: Long Non-Coding RNA RAB11B-AS1 Suppresses Cervical Cancer Progression by Upregulating RPL26 Expression
Article Snippet: .. Construction of the sequencing library and RNA-sequencing (RNA-seq) were performed by Beijing Novogene Company. ..



Similar Products

86
10X Genomics sequencing chromium single cell 3 library gel bead kit v2
Sequencing Chromium Single Cell 3 Library Gel Bead Kit V2, supplied by 10X Genomics, 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/sequencing+library/cellranger/pmc08772395-882-0-12
Average 86 stars, based on 1 article reviews
sequencing chromium single cell 3 library gel bead kit v2 - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
10X Genomics sequencing chromium single cell 3 library gel bead kit v3
Sequencing Chromium Single Cell 3 Library Gel Bead Kit V3, supplied by 10X Genomics, 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/sequencing+library/cellranger/pmc08772395-883-0-12
Average 86 stars, based on 1 article reviews
sequencing chromium single cell 3 library gel bead kit v3 - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Novogene sequencing libraries
Sequencing Libraries, 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/sequencing+library/libraries+sequencing/pmc13156682-346-0-11
Average 86 stars, based on 1 article reviews
sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Pacific Biosciences sequencing libraries
Sequencing Libraries, supplied by Pacific Biosciences, 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/sequencing+library/circular+consensus+dna+hifi+libraries+sequencing/pm42286965-99-0-15
Average 86 stars, based on 1 article reviews
sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Pacific Biosciences hifi circular consensus dna sequencing libraries
Hifi Circular Consensus Dna Sequencing Libraries, supplied by Pacific Biosciences, 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/sequencing+library/circular+consensus+dna+hifi+libraries+sequencing/pm42270437-85-2-0
Average 86 stars, based on 1 article reviews
hifi circular consensus dna sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Novogene rna sequencing libraries
Rna Sequencing Libraries, 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/sequencing+library/libraries+rna+seq/pm42269550-91-0-8
Average 86 stars, based on 1 article reviews
rna sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Twist Bioscience barcode sequencing landing pad 77 a site saturation mutagenesis library
Barcode Sequencing Landing Pad 77 A Site Saturation Mutagenesis Library, supplied by Twist Bioscience, 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/sequencing+library/library+saturation+site+variant/pm42248140-291-29-40
Average 86 stars, based on 1 article reviews
barcode sequencing landing pad 77 a site saturation mutagenesis library - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Macrogen short read sequencing libraries
Gene expression in control samples was compared between CD4+ and CD8+ samples (A) Proportion of all genes, immune genes and T1D genes that are differentially expressed between CD4+ and CD8+ control samples. T1D candidate genes and immune relevant genes are more likely to be differentially expressed between these cell types. (B) Annotated and detected exon and intron features for T1D candidate gene UBASH3A. From bottom to top i) The reference MANE transcript ii) all annotated features in Refseq/Ensembl iii) Exon/Intron features detected by long read <t>sequencing</t> in both cell types iii) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) iv) Exon/Intron features detected in CD8+ RNA-seq samples (n=98). Exon Region 5 of UBASH3A is differentially detected between CD4+ and CD8+. (C) Proportion of all genes, immune genes and T1D genes with at least one differentially detected feature between CD4+ and CD8+samples. T1D genes are more likely to have differentially detected exon/intron features between CD4+ and CD8+ cells.
Short Read Sequencing Libraries, supplied by Macrogen, 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/sequencing+library/libraries+read+sequencing+short/bio_rxiv__64898__2026__05__29__728908-59-1-23
Average 86 stars, based on 1 article reviews
short read sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

86
Pacific Biosciences smrtbell sequencing libraries
Gene expression in control samples was compared between CD4+ and CD8+ samples (A) Proportion of all genes, immune genes and T1D genes that are differentially expressed between CD4+ and CD8+ control samples. T1D candidate genes and immune relevant genes are more likely to be differentially expressed between these cell types. (B) Annotated and detected exon and intron features for T1D candidate gene UBASH3A. From bottom to top i) The reference MANE transcript ii) all annotated features in Refseq/Ensembl iii) Exon/Intron features detected by long read <t>sequencing</t> in both cell types iii) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) iv) Exon/Intron features detected in CD8+ RNA-seq samples (n=98). Exon Region 5 of UBASH3A is differentially detected between CD4+ and CD8+. (C) Proportion of all genes, immune genes and T1D genes with at least one differentially detected feature between CD4+ and CD8+samples. T1D genes are more likely to have differentially detected exon/intron features between CD4+ and CD8+ cells.
Smrtbell Sequencing Libraries, supplied by Pacific Biosciences, 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/sequencing+library/libraries+smrtbell/10__1016_slash_j__dib__2026__112970-192-0-25
Average 86 stars, based on 1 article reviews
smrtbell sequencing libraries - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

Image Search Results


Gene expression in control samples was compared between CD4+ and CD8+ samples (A) Proportion of all genes, immune genes and T1D genes that are differentially expressed between CD4+ and CD8+ control samples. T1D candidate genes and immune relevant genes are more likely to be differentially expressed between these cell types. (B) Annotated and detected exon and intron features for T1D candidate gene UBASH3A. From bottom to top i) The reference MANE transcript ii) all annotated features in Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iii) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) iv) Exon/Intron features detected in CD8+ RNA-seq samples (n=98). Exon Region 5 of UBASH3A is differentially detected between CD4+ and CD8+. (C) Proportion of all genes, immune genes and T1D genes with at least one differentially detected feature between CD4+ and CD8+samples. T1D genes are more likely to have differentially detected exon/intron features between CD4+ and CD8+ cells.

Journal: bioRxiv

Article Title: Sex and Alternative Splicing in Disease: a meta-analytic approach to identify interactions

doi: 10.64898/2026.05.29.728908

Figure Lengend Snippet: Gene expression in control samples was compared between CD4+ and CD8+ samples (A) Proportion of all genes, immune genes and T1D genes that are differentially expressed between CD4+ and CD8+ control samples. T1D candidate genes and immune relevant genes are more likely to be differentially expressed between these cell types. (B) Annotated and detected exon and intron features for T1D candidate gene UBASH3A. From bottom to top i) The reference MANE transcript ii) all annotated features in Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iii) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) iv) Exon/Intron features detected in CD8+ RNA-seq samples (n=98). Exon Region 5 of UBASH3A is differentially detected between CD4+ and CD8+. (C) Proportion of all genes, immune genes and T1D genes with at least one differentially detected feature between CD4+ and CD8+samples. T1D genes are more likely to have differentially detected exon/intron features between CD4+ and CD8+ cells.

Article Snippet: ; Short read sequencing libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep kit (New England BioLabs) and sequenced by Macrogen.

Techniques: Gene Expression, Control, Sequencing, RNA Sequencing

A) Annotated and detected exon and intron patterns for T1D candidate gene RPAP2. From bottom to top i) The reference MANE transcript ii) all annotated features in either Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iv) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) Exon regions 1,4 and 7 are labelled. (B) – (D) Normalized expression level (log uq APN) of exon regions 1,4 and 7 stratified by sex and T1D status. Log UQ APN of 3 is shown with black dotted line across all plots. (E)-(G) Effect size of T1D on exon regions 1,4 and 7 stratified by sex in CD4+ RNA-seq samples. A positive effect size indicates that controls are more highly expressed than cases and a negative effect size indicates that cases are more highly expressed than controls for a given feature. Effect size of 0 is represented by the black dotted line. The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature.

Journal: bioRxiv

Article Title: Sex and Alternative Splicing in Disease: a meta-analytic approach to identify interactions

doi: 10.64898/2026.05.29.728908

Figure Lengend Snippet: A) Annotated and detected exon and intron patterns for T1D candidate gene RPAP2. From bottom to top i) The reference MANE transcript ii) all annotated features in either Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iv) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) Exon regions 1,4 and 7 are labelled. (B) – (D) Normalized expression level (log uq APN) of exon regions 1,4 and 7 stratified by sex and T1D status. Log UQ APN of 3 is shown with black dotted line across all plots. (E)-(G) Effect size of T1D on exon regions 1,4 and 7 stratified by sex in CD4+ RNA-seq samples. A positive effect size indicates that controls are more highly expressed than cases and a negative effect size indicates that cases are more highly expressed than controls for a given feature. Effect size of 0 is represented by the black dotted line. The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature.

Article Snippet: ; Short read sequencing libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep kit (New England BioLabs) and sequenced by Macrogen.

Techniques: Sequencing, RNA Sequencing, Expressing

(A) Annotated and detected exon and intron patterns for T1D candidate gene STRN4. From bottom to top i)The reference MANE transcript ii) all annotated features in either Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iv) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) (B) Normalized expression level (log_uq_apn) of CD4+ RNASeq samples for all features of the T1D candidate gene STRN4. There are differential rates of exon and intron feature inclusion across the length of the transcript (C) Effect size of T1D on all exon/intron features in STRN4 stratified by sex in CD4+ RNA-seq samples. The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature. Pvalue for the test of heterogeneity of female and male effect sizes and the Pvalue for the test of a moderator (sex) effect on the whole gene is shown. The test for heterogeneity is significant for females but not for males indicating that there is differential splicing between T1D cases and controls in female samples for the STRN4 gene. The test for moderator (sex) effect is significant indicating that there is an overall effect of sex on the gene.

Journal: bioRxiv

Article Title: Sex and Alternative Splicing in Disease: a meta-analytic approach to identify interactions

doi: 10.64898/2026.05.29.728908

Figure Lengend Snippet: (A) Annotated and detected exon and intron patterns for T1D candidate gene STRN4. From bottom to top i)The reference MANE transcript ii) all annotated features in either Refseq/Ensembl iii) Exon/Intron features detected by long read sequencing in both cell types iv) Exon/Intron features detected in CD4+ RNA-seq samples (n=113) (B) Normalized expression level (log_uq_apn) of CD4+ RNASeq samples for all features of the T1D candidate gene STRN4. There are differential rates of exon and intron feature inclusion across the length of the transcript (C) Effect size of T1D on all exon/intron features in STRN4 stratified by sex in CD4+ RNA-seq samples. The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature. Pvalue for the test of heterogeneity of female and male effect sizes and the Pvalue for the test of a moderator (sex) effect on the whole gene is shown. The test for heterogeneity is significant for females but not for males indicating that there is differential splicing between T1D cases and controls in female samples for the STRN4 gene. The test for moderator (sex) effect is significant indicating that there is an overall effect of sex on the gene.

Article Snippet: ; Short read sequencing libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep kit (New England BioLabs) and sequenced by Macrogen.

Techniques: Sequencing, RNA Sequencing, Expressing, RNA sequencing

A) Number and proportion of analyzable T1D genes with a 3-way interaction effect interaction of sex,splicing and T1D status for CD4+ and CD8+ samples. A higher proportion of T1D genes have a sex*splicing*T1D effect in CD4+ samples compared to CD8+ samples B) Annotated and detected exon patterns for T1D candidate gene BACH2. From bottom to top i) The reference MANE transcript ii) all annotated exons in Refseq/Ensembl iii) Exon features detected by long read sequencing in both cell types iii) Exon features detected in CD4+ RNA-seq samples (n=113) iv) Exon feautures detected in CD8+ RNA-seq samples (n=98). C) Effect size of T1D on all exonic features in BACH2 stratified by sex in CD4+ RNA-seq samples (top) and CD8+ RNA-seq samples (bottom). The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature. Pvalue for the test of heterogeneity of female and male effect sizes and the Pvalue for test of a moderator (sex) effect on the whole gene is shown. In CD4, the test for heterogeneity is significant for females but not for males indicating that there is differential splicing between T1D cases and controls in female samples for the BACH2 gene. The inverse effect is observed in CD8+ samples where we observe an effect of T1D on splicing in males but not females. Pvalue for the test of the 3-way interaction of sex, T1D and splicing differences is shown. This test of heterogeneity tests for the interaction of sex and splicing. Both CD4+ and CD8+ have a 3-way T1D*sex*splicing effect in the BACH2 gene.

Journal: bioRxiv

Article Title: Sex and Alternative Splicing in Disease: a meta-analytic approach to identify interactions

doi: 10.64898/2026.05.29.728908

Figure Lengend Snippet: A) Number and proportion of analyzable T1D genes with a 3-way interaction effect interaction of sex,splicing and T1D status for CD4+ and CD8+ samples. A higher proportion of T1D genes have a sex*splicing*T1D effect in CD4+ samples compared to CD8+ samples B) Annotated and detected exon patterns for T1D candidate gene BACH2. From bottom to top i) The reference MANE transcript ii) all annotated exons in Refseq/Ensembl iii) Exon features detected by long read sequencing in both cell types iii) Exon features detected in CD4+ RNA-seq samples (n=113) iv) Exon feautures detected in CD8+ RNA-seq samples (n=98). C) Effect size of T1D on all exonic features in BACH2 stratified by sex in CD4+ RNA-seq samples (top) and CD8+ RNA-seq samples (bottom). The upper and lower bounds of the 95% confidence interval for the effect size are shown for each feature. Pvalue for the test of heterogeneity of female and male effect sizes and the Pvalue for test of a moderator (sex) effect on the whole gene is shown. In CD4, the test for heterogeneity is significant for females but not for males indicating that there is differential splicing between T1D cases and controls in female samples for the BACH2 gene. The inverse effect is observed in CD8+ samples where we observe an effect of T1D on splicing in males but not females. Pvalue for the test of the 3-way interaction of sex, T1D and splicing differences is shown. This test of heterogeneity tests for the interaction of sex and splicing. Both CD4+ and CD8+ have a 3-way T1D*sex*splicing effect in the BACH2 gene.

Article Snippet: ; Short read sequencing libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep kit (New England BioLabs) and sequenced by Macrogen.

Techniques: Sequencing, RNA Sequencing