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MGI Tech Co Ltd dnbseq-t7 sequencer pe150
Dnbseq T7 Sequencer Pe150, supplied by MGI Tech Co 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/dnbseq-t7+sequencer+pe150/dnbseq+t7+sequencer+pe150/pmc12064995-85-37-30
Average 90 stars, based on 1 article reviews
dnbseq-t7 sequencer pe150 - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Control:

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis.
Article Snippet: Meiosis in males is a critical process that ensures complete spermatogenesis and genetic diversity.. However, the key regulators involved in this process and the underlying molecular mechanisms remain unclear.. Here, we report an essential role of the m6A methyltransferase METTL16 in meiotic sex chromosome inactivation (MSCI), double-strand break (DSB) formation, homologous recombination and SYCP1 deposition during male meiosis.

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis
Article Snippet: 200–500 bps library products were enriched, quantified, and sequenced on DNBSEQ‐T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model.

Article Title: Anaerobic metabolism promotes breast cancer survival via Histone-3 Lysine-18 lactylation mediating PPARD axis.
Article Snippet: The library was enriched for 200–500 bps fragments, quantified, and sequenced on DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model [39].

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ‐T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: Expression and prognostic significance of the m6A RNA methylation regulator HNRNPC in HNSCC
Article Snippet: The library products corresponding to 200–500 bps were enriched, quantitated, and then sequenced and analyzed on the DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model. Gene Ontology (GO) enrichment analysis was performed using the KOBAS software (version: 2.1.1) to determine the biological implications of the differentially expressed genes (DEGs).

Article Title: Exploring the infection strategy of Colletotrichum fructicola in pecan and two effectors Cf-ID1 and Cf-ID2 were characterized using unique molecular identifier-RNA sequencing technology
Article Snippet: The library products corresponding to 200-500 bps were enriched, quantified, and finally sequenced on a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model.

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1.
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ- T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: METTL3 mediated m6A modification of HKDC1 promotes renal injury and inflammation in lead nephropathy
Article Snippet: PCR products corresponding to 200-500 bp were enriched, quantified, and sequenced using a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) using a PE150 model.

cDNA Library Assay:

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis.
Article Snippet: Meiosis in males is a critical process that ensures complete spermatogenesis and genetic diversity.. However, the key regulators involved in this process and the underlying molecular mechanisms remain unclear.. Here, we report an essential role of the m6A methyltransferase METTL16 in meiotic sex chromosome inactivation (MSCI), double-strand break (DSB) formation, homologous recombination and SYCP1 deposition during male meiosis.

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis
Article Snippet: 200–500 bps library products were enriched, quantified, and sequenced on DNBSEQ‐T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model.

Article Title: Anaerobic metabolism promotes breast cancer survival via Histone-3 Lysine-18 lactylation mediating PPARD axis.
Article Snippet: The library was enriched for 200–500 bps fragments, quantified, and sequenced on DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model [39].

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ‐T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: Expression and prognostic significance of the m6A RNA methylation regulator HNRNPC in HNSCC
Article Snippet: The library products corresponding to 200–500 bps were enriched, quantitated, and then sequenced and analyzed on the DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model. Gene Ontology (GO) enrichment analysis was performed using the KOBAS software (version: 2.1.1) to determine the biological implications of the differentially expressed genes (DEGs).

Article Title: Exploring the infection strategy of Colletotrichum fructicola in pecan and two effectors Cf-ID1 and Cf-ID2 were characterized using unique molecular identifier-RNA sequencing technology
Article Snippet: The library products corresponding to 200-500 bps were enriched, quantified, and finally sequenced on a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model.

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1.
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ- T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: METTL3 mediated m6A modification of HKDC1 promotes renal injury and inflammation in lead nephropathy
Article Snippet: PCR products corresponding to 200-500 bp were enriched, quantified, and sequenced using a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) using a PE150 model.

Software:

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis.
Article Snippet: Meiosis in males is a critical process that ensures complete spermatogenesis and genetic diversity.. However, the key regulators involved in this process and the underlying molecular mechanisms remain unclear.. Here, we report an essential role of the m6A methyltransferase METTL16 in meiotic sex chromosome inactivation (MSCI), double-strand break (DSB) formation, homologous recombination and SYCP1 deposition during male meiosis.

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis
Article Snippet: 200–500 bps library products were enriched, quantified, and sequenced on DNBSEQ‐T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model.

Article Title: Anaerobic metabolism promotes breast cancer survival via Histone-3 Lysine-18 lactylation mediating PPARD axis.
Article Snippet: The library was enriched for 200–500 bps fragments, quantified, and sequenced on DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model [39].

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ‐T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: Expression and prognostic significance of the m6A RNA methylation regulator HNRNPC in HNSCC
Article Snippet: The library products corresponding to 200–500 bps were enriched, quantitated, and then sequenced and analyzed on the DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model. Gene Ontology (GO) enrichment analysis was performed using the KOBAS software (version: 2.1.1) to determine the biological implications of the differentially expressed genes (DEGs).

Article Title: Exploring the infection strategy of Colletotrichum fructicola in pecan and two effectors Cf-ID1 and Cf-ID2 were characterized using unique molecular identifier-RNA sequencing technology
Article Snippet: The library products corresponding to 200-500 bps were enriched, quantified, and finally sequenced on a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model.

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1.
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ- T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: METTL3 mediated m6A modification of HKDC1 promotes renal injury and inflammation in lead nephropathy
Article Snippet: PCR products corresponding to 200-500 bp were enriched, quantified, and sequenced using a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) using a PE150 model.

Sequencing:

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis.
Article Snippet: Meiosis in males is a critical process that ensures complete spermatogenesis and genetic diversity.. However, the key regulators involved in this process and the underlying molecular mechanisms remain unclear.. Here, we report an essential role of the m6A methyltransferase METTL16 in meiotic sex chromosome inactivation (MSCI), double-strand break (DSB) formation, homologous recombination and SYCP1 deposition during male meiosis.

Article Title: METTL16 is Required for Meiotic Sex Chromosome Inactivation and DSB Formation and Recombination during Male Meiosis
Article Snippet: 200–500 bps library products were enriched, quantified, and sequenced on DNBSEQ‐T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model.

Article Title: Anaerobic metabolism promotes breast cancer survival via Histone-3 Lysine-18 lactylation mediating PPARD axis.
Article Snippet: The library was enriched for 200–500 bps fragments, quantified, and sequenced on DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with PE150 model [39].

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ‐T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: Expression and prognostic significance of the m6A RNA methylation regulator HNRNPC in HNSCC
Article Snippet: The library products corresponding to 200–500 bps were enriched, quantitated, and then sequenced and analyzed on the DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model. Gene Ontology (GO) enrichment analysis was performed using the KOBAS software (version: 2.1.1) to determine the biological implications of the differentially expressed genes (DEGs).

Article Title: Exploring the infection strategy of Colletotrichum fructicola in pecan and two effectors Cf-ID1 and Cf-ID2 were characterized using unique molecular identifier-RNA sequencing technology
Article Snippet: The library products corresponding to 200-500 bps were enriched, quantified, and finally sequenced on a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) with the PE150 model.

Article Title: The Potential Hepatocyte Differentiation Targets and MSC Proliferation by FH1.
Article Snippet: After quality control of the RNA amount, purity and integrity, 200–500 bp cDNA library products from 2 μg of total RNA were quantified and finally sequenced on a DNBSEQ- T7 sequencer (MGI Tech Co. Ltd., China) with the PE150 model. Differentially expressed genes were defined as those with a fold change > 2 or < 0.5 and p < 0.05, and then GO analysis and KEGG enrichment analysis were both implemented with KOBAS software (version 2.1.1).

Article Title: METTL3 mediated m6A modification of HKDC1 promotes renal injury and inflammation in lead nephropathy
Article Snippet: PCR products corresponding to 200-500 bp were enriched, quantified, and sequenced using a DNBSEQ-T7 sequencer (MGI Tech Co., Ltd. China) using a PE150 model.



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