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  4. High Throughput RNA-seq unveils Transcriptome Mystery at Novogene

High Throughput RNA-seq unveils Transcriptome Mystery at Novogene

Transcriptome analysis examines the complete set of RNA transcripts in a cell using high-throughput RNA-sequencing (RNA-seq). This valuable tool provides important information on gene function in a cell, a population of cells, or in an organism, that are under a specific set of conditions. RNA-seq identifies all RNA transcripts in a sample, including the regulatory miRNA and lncRNA transcripts. The sequences obtained by these methods can then be aligned to reference sequences to identify which genes have been transcribed in the sample.

Novogene is a leading genomics solution provider that offers a wide range of transcriptome sequencing services ranging from mRNA-sequencing to whole transcriptome analysis. With 29 next-generation sequencing (NGS) -related patents and over 560 research papers, Novogene is a world leader in next- NGS services. Novogene’s services offer comprehensive solutions for the analysis of gene expression quantification and differential gene expression, the identification of novel transcripts, examining alternative splicing and gene fusion events, and more. The company’s bioinformaticians provide standard and customized data analysis, resulting in publication-ready results.

The experimental objective should dictate the type of sequencing that is used. For example, mRNA-sequencing ( mRNA-seq) focuses only on the coding RNAs, which make up approximately 2% of the entire transcriptome. This type of sequencing is ideal if research focuses only on these coding regions. mRNA-seq enables researchers to examine the variations in the cellular transcriptome by looking at the mRNA expression levels in a biological sample. It is often used to identify or compare gene expression levels between groups. Novogene’s mRNA-seq is performed on the Illumina NovaSeq platforms with paired-end 150 base pair sequencing read length. The sequencing depth varies based on whether a reference genome is available.

By comparison, whole transcriptome sequencing (WTS) looks at the set of genes that are transcribed by an organism at any given moment and includes all coding and non-coding RNA transcripts. This competitive approach is particularly useful for understanding what genes are being transcribed under different conditions. Once the transcriptome has been sequenced, the information can be used to ascertain which parts of the genome codes for active genes. This can be taken further by sequencing the transcriptome several times under different conditions or at different life stages to help understand which genes are involved in which biological processes. Novogene’s WTS service enables researchers to investigate potential transcriptional and regulatory network mechanisms by enabling an in-depth bioinformatics analysis on all transcripts including mRNAs and non-coding RNAs.

Aside from mRNA-seq and WTS, Novogene offers other transcriptome sequencing services including metatranscriptome analysis which examines the total content of gene transcripts in a community, such as soil, water, or in the gut, prokaryote RNA-sequencing, and an isoform-sequencing service that can be useful for detecting gene fusion events as well as providing more in-depth transcript annotation. To improve the accuracy of their next-generation sequencing services further, Novogene launched a new product named Falcon in March 2020. Falcon is the first intelligent multi-product delivery platform for high-throughput NGS. Falcon promises to offer faster delivery with a more stable quality by eliminating human error and increasing efficiency. This platform will provide Novogene’s customers with an intelligent and robust service that can process up to 2850 samples each day. This new platform aims to increase the quality of Novogene’s services and meet the sequencing requirements of its customers.

The founder and CEO of Novogene, Dr. Li Ruiqiang said, “Leveraging our years of expertise in genomic sequencing has enabled Novogene to develop and launch the first intelligent multi-product NGS delivery platform, which will provide a cutting-edge sequencing solution for customers. As a safe and accurate one-stop ground-breaking solution, Falcon enables faster delivery with a more stable quality. As a leading provider of genomic services and solutions in the world, we want to be better positioned to drive innovation in the industry, to lead the industry in the direction towards becoming digital and automated, to propel the establishment of industry standards, and to eventually achieve intelligent transformation.”

To get more information about Novogene services, please visit novogene.com/amea-en. Contact us at here (https://bit.ly/33b97Wi). Your dedicated Novogene representative will reach out to you within ONE business day.

Transcriptome analysis examines the complete set of RNA transcripts in a cell using high-throughput RNA-sequencing (RNA-seq). This valuable tool provides important information on gene function in a cell, a population of cells, or in an organism, that are under a specific set of conditions. RNA-seq identifies all RNA transcripts in a sample, including the regulatory miRNA and lncRNA transcripts. The sequences obtained by these methods can then be aligned to reference sequences to identify which genes have been transcribed in the sample.

Novogene is a leading genomics solution provider that offers a wide range of transcriptome sequencing services ranging from mRNA-sequencing to whole transcriptome analysis. With 29 next-generation sequencings (NGS) – related patents and over 560 research papers, Novogene is a world leader in next- NGS services. Novogene’s services offer comprehensive solutions for the analysis of gene expression quantification and differential gene expression, the identification of novel transcripts, examining alternative splicing and gene fusion events, and more. The company’s bioinformaticians provide standard and customized data analysis, resulting in publication-ready results.

The experimental objective should dictate the type of sequencing that is used. For example, mRNA-sequencing ( mRNA-seq) focuses only on the coding RNAs, which make up approximately 2% of the entire transcriptome. This type of sequencing is ideal if research focuses only on these coding regions. mRNA-seq enables researchers to examine the variations in the cellular transcriptome by looking at the mRNA expression levels in a biological sample. It is often used to identify or compare gene expression levels between groups. Novogene’s mRNA-seq is performed on the Illumina NovaSeq platforms with paired-end 150 base pair sequencing read length. The sequencing depth varies based on whether a reference genome is available.

By comparison, whole transcriptome sequencing (WTS) looks at the set of genes that are transcribed by an organism at any given moment and includes all coding and non-coding RNA transcripts. This competitive approach is particularly useful for understanding what genes are being transcribed under different conditions. Once the transcriptome has been sequenced, the information can be used to ascertain which parts of the genome codes for active genes. This can be taken further by sequencing the transcriptome several times under different conditions or at different life stages to help understand which genes are involved in which biological processes. Novogene’s WTS service enables researchers to investigate potential transcriptional and regulatory network mechanisms by enabling an in-depth bioinformatics analysis on all transcripts including mRNAs and non-coding RNAs

Aside from mRNA-seq and WTS, Novogene offers other transcriptome sequencing services including metatranscriptome analysis which examines the total content of gene transcripts in a community, such as soil, water, or in the gut, prokaryote RNA-sequencing, and an isoform-sequencing service that can be useful for detecting gene fusion events as well as providing more in-depth transcript annotation.

To improve the accuracy of their next-generation sequencing services further, Novogene launched a new product named Falcon in March 2020. Falcon is the first intelligent multi-product delivery platform for high-throughput NGS. Falcon promises to offer faster delivery with a more stable quality by eliminating human error and increasing efficiency. This platform will provide Novogene’s customers with an intelligent and robust service that can process up to 2850 samples each day. This new platform aims to increase the quality of Novogene’s services and meet the sequencing requirements of its customers.

The founder and CEO of Novogene, Dr Li Ruiqiang said, “Leveraging our years of expertise in genomic sequencing has enabled Novogene to develop and launch the first intelligent multi-product NGS delivery platform, which will provide a cutting-edge sequencing solution for customers. As a safe and accurate one-stop ground-breaking solution, Falcon enables faster delivery with more stable quality. As a leading provider of genomic services and solutions in the world, we want to be better positioned to drive innovation in the industry, to lead the industry in the direction towards becoming digital and automated, to propel the establishment of industry standards, and to eventually achieve intelligent transformation.”

To get more information about Novogene services, please visit our website: novogene.com/amea-en Or contact us here. Your dedicated Novogene representative will reach out to you within ONE business day.

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全ゲノムシーケンスde novoシーケンスアンプリコンシーケンスショットガンメタゲノムシーケンスディレクトDNAメチレーションシーケンス(DM-Seq)mRNAシーケンスシングルセル遺伝子発現解析Olinkプロテオミクス
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Copyright © 2026 Novogene Inc. All rights reserved. 本サービスは研究目的のみにご利用ください。臨床診断目的には使用頂けません。
ノボジーン
  • ノボジーン
  • ゲノミクス
    • ヒト全ゲノムシーケンス
    • 動植物全ゲノムシーケンス
    • 微生物全ゲノムシーケンス
    • 動植物de novoシーケンス
    • 微生物de novoシーケンス
    • ショットガンメタゲノムシーケンス
    • アンプリコンシーケンス
    • 全エクソームシーケンス
    トランスクリプトミクス
    • mRNAシーケンス
    • トータルRNAシーケンス
    • 全長トランスクリプトームシーケンス
    • 全トランスクリプトームシーケンス
    • スモールRNAシーケンシング
    • 環状RNAシーケンス
    • メタトランスクリプトームシーケンス
    • 原核生物RNAシーケンス
    シングルセルと空間オミクス
    • シングルセル遺伝子発現解析
    • シングルセル免疫プロファイリングシーケンス
    • シングルセルロングリードトランスクリプトーム
    エピゲノミクス
    • 全ゲノムバイサルファイトシーケンス(WGBS)
    • ディレクトDNAメチレーションシーケンス(DM-Seq)new
    • 還元型バイサルファイトシーケンス (RRBS)
    • クロマチン免疫沈降シーケンス(ChIP-Seq)
    • RNA免疫沈降シーケンス (RIP-Seq)

    相乗りシーケンス

    • 相乗りシーケンス(イルミナプラットフォーム)
    • 相乗りシーケンス(PacBioプラットフォーム)
    プロテオミクス & メタボロミクス
    • Olinkプロテオミクス
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  1. Home
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  4. High Throughput RNA-seq unveils Transcriptome Mystery at Novogene

High Throughput RNA-seq unveils Transcriptome Mystery at Novogene

Transcriptome analysis examines the complete set of RNA transcripts in a cell using high-throughput RNA-sequencing (RNA-seq). This valuable tool provides important information on gene function in a cell, a population of cells, or in an organism, that are under a specific set of conditions. RNA-seq identifies all RNA transcripts in a sample, including the regulatory miRNA and lncRNA transcripts. The sequences obtained by these methods can then be aligned to reference sequences to identify which genes have been transcribed in the sample.

Novogene is a leading genomics solution provider that offers a wide range of transcriptome sequencing services ranging from mRNA-sequencing to whole transcriptome analysis. With 29 next-generation sequencing (NGS) -related patents and over 560 research papers, Novogene is a world leader in next- NGS services. Novogene’s services offer comprehensive solutions for the analysis of gene expression quantification and differential gene expression, the identification of novel transcripts, examining alternative splicing and gene fusion events, and more. The company’s bioinformaticians provide standard and customized data analysis, resulting in publication-ready results.

The experimental objective should dictate the type of sequencing that is used. For example, mRNA-sequencing ( mRNA-seq) focuses only on the coding RNAs, which make up approximately 2% of the entire transcriptome. This type of sequencing is ideal if research focuses only on these coding regions. mRNA-seq enables researchers to examine the variations in the cellular transcriptome by looking at the mRNA expression levels in a biological sample. It is often used to identify or compare gene expression levels between groups. Novogene’s mRNA-seq is performed on the Illumina NovaSeq platforms with paired-end 150 base pair sequencing read length. The sequencing depth varies based on whether a reference genome is available.

By comparison, whole transcriptome sequencing (WTS) looks at the set of genes that are transcribed by an organism at any given moment and includes all coding and non-coding RNA transcripts. This competitive approach is particularly useful for understanding what genes are being transcribed under different conditions. Once the transcriptome has been sequenced, the information can be used to ascertain which parts of the genome codes for active genes. This can be taken further by sequencing the transcriptome several times under different conditions or at different life stages to help understand which genes are involved in which biological processes. Novogene’s WTS service enables researchers to investigate potential transcriptional and regulatory network mechanisms by enabling an in-depth bioinformatics analysis on all transcripts including mRNAs and non-coding RNAs.

Aside from mRNA-seq and WTS, Novogene offers other transcriptome sequencing services including metatranscriptome analysis which examines the total content of gene transcripts in a community, such as soil, water, or in the gut, prokaryote RNA-sequencing, and an isoform-sequencing service that can be useful for detecting gene fusion events as well as providing more in-depth transcript annotation. To improve the accuracy of their next-generation sequencing services further, Novogene launched a new product named Falcon in March 2020. Falcon is the first intelligent multi-product delivery platform for high-throughput NGS. Falcon promises to offer faster delivery with a more stable quality by eliminating human error and increasing efficiency. This platform will provide Novogene’s customers with an intelligent and robust service that can process up to 2850 samples each day. This new platform aims to increase the quality of Novogene’s services and meet the sequencing requirements of its customers.

The founder and CEO of Novogene, Dr. Li Ruiqiang said, “Leveraging our years of expertise in genomic sequencing has enabled Novogene to develop and launch the first intelligent multi-product NGS delivery platform, which will provide a cutting-edge sequencing solution for customers. As a safe and accurate one-stop ground-breaking solution, Falcon enables faster delivery with a more stable quality. As a leading provider of genomic services and solutions in the world, we want to be better positioned to drive innovation in the industry, to lead the industry in the direction towards becoming digital and automated, to propel the establishment of industry standards, and to eventually achieve intelligent transformation.”

To get more information about Novogene services, please visit novogene.com/amea-en. Contact us at here (https://bit.ly/33b97Wi). Your dedicated Novogene representative will reach out to you within ONE business day.

Transcriptome analysis examines the complete set of RNA transcripts in a cell using high-throughput RNA-sequencing (RNA-seq). This valuable tool provides important information on gene function in a cell, a population of cells, or in an organism, that are under a specific set of conditions. RNA-seq identifies all RNA transcripts in a sample, including the regulatory miRNA and lncRNA transcripts. The sequences obtained by these methods can then be aligned to reference sequences to identify which genes have been transcribed in the sample.

Novogene is a leading genomics solution provider that offers a wide range of transcriptome sequencing services ranging from mRNA-sequencing to whole transcriptome analysis. With 29 next-generation sequencings (NGS) – related patents and over 560 research papers, Novogene is a world leader in next- NGS services. Novogene’s services offer comprehensive solutions for the analysis of gene expression quantification and differential gene expression, the identification of novel transcripts, examining alternative splicing and gene fusion events, and more. The company’s bioinformaticians provide standard and customized data analysis, resulting in publication-ready results.

The experimental objective should dictate the type of sequencing that is used. For example, mRNA-sequencing ( mRNA-seq) focuses only on the coding RNAs, which make up approximately 2% of the entire transcriptome. This type of sequencing is ideal if research focuses only on these coding regions. mRNA-seq enables researchers to examine the variations in the cellular transcriptome by looking at the mRNA expression levels in a biological sample. It is often used to identify or compare gene expression levels between groups. Novogene’s mRNA-seq is performed on the Illumina NovaSeq platforms with paired-end 150 base pair sequencing read length. The sequencing depth varies based on whether a reference genome is available.

By comparison, whole transcriptome sequencing (WTS) looks at the set of genes that are transcribed by an organism at any given moment and includes all coding and non-coding RNA transcripts. This competitive approach is particularly useful for understanding what genes are being transcribed under different conditions. Once the transcriptome has been sequenced, the information can be used to ascertain which parts of the genome codes for active genes. This can be taken further by sequencing the transcriptome several times under different conditions or at different life stages to help understand which genes are involved in which biological processes. Novogene’s WTS service enables researchers to investigate potential transcriptional and regulatory network mechanisms by enabling an in-depth bioinformatics analysis on all transcripts including mRNAs and non-coding RNAs

Aside from mRNA-seq and WTS, Novogene offers other transcriptome sequencing services including metatranscriptome analysis which examines the total content of gene transcripts in a community, such as soil, water, or in the gut, prokaryote RNA-sequencing, and an isoform-sequencing service that can be useful for detecting gene fusion events as well as providing more in-depth transcript annotation.

To improve the accuracy of their next-generation sequencing services further, Novogene launched a new product named Falcon in March 2020. Falcon is the first intelligent multi-product delivery platform for high-throughput NGS. Falcon promises to offer faster delivery with a more stable quality by eliminating human error and increasing efficiency. This platform will provide Novogene’s customers with an intelligent and robust service that can process up to 2850 samples each day. This new platform aims to increase the quality of Novogene’s services and meet the sequencing requirements of its customers.

The founder and CEO of Novogene, Dr Li Ruiqiang said, “Leveraging our years of expertise in genomic sequencing has enabled Novogene to develop and launch the first intelligent multi-product NGS delivery platform, which will provide a cutting-edge sequencing solution for customers. As a safe and accurate one-stop ground-breaking solution, Falcon enables faster delivery with more stable quality. As a leading provider of genomic services and solutions in the world, we want to be better positioned to drive innovation in the industry, to lead the industry in the direction towards becoming digital and automated, to propel the establishment of industry standards, and to eventually achieve intelligent transformation.”

To get more information about Novogene services, please visit our website: novogene.com/amea-en Or contact us here. Your dedicated Novogene representative will reach out to you within ONE business day.

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サービス
全ゲノムシーケンスde novoシーケンスアンプリコンシーケンスショットガンメタゲノムシーケンスディレクトDNAメチレーションシーケンス(DM-Seq)mRNAシーケンスシングルセル遺伝子発現解析Olinkプロテオミクス
サポート
バイオインフォマティクス解析ツール(NovoMagic)カスタマサービスシステム(CSS)インテリジェント自動化プラットフォーム(Falcon)
会社
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Copyright © 2026 Novogene Inc. All rights reserved. 本サービスは研究目的のみにご利用ください。臨床診断目的には使用頂けません。
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