Novogene Korea
  • Novogene Korea
  • Genomics
    • Human Whole Genome Sequencing
    • Plant & Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant & Animal De novo Sequencing
    • Microbial De novo Sequencing
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    Transcriptomics
    • mRNA Sequencing
    • Total RNA Sequencing
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    • Whole Transcriptome Sequencing
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    • Stereo-Seq Spatial Gene Expression
    • Xenium In Situ Spatial Transcriptome
    Epigenomics
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Directed DNA Methylation Sequencing (DM-Seq) NEW
    • Reduced Representation Bisulfite Sequencing (RRBS)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)

    Premade Library

    • Sequencing Only (Illumina 플랫폼)
    • Sequencing Only (PacBio 플랫폼)
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    • Olink Proteomics
    • Quantitative Proteomics (MS)
    • Untargeted Metabolomics (MS)
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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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WGSDe novo SeqAmplicon SeqShotgun MetagenomeDM-SeqmRNA-SeqSingle Cell Gene ExpressionVisium HDXenium In SituOlinkUntargeted Metabolomics
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Copyright © 2026 Novogene Co., Ltd. All Rights Reserved. 노보진의 한국 내 모든 서비스는 연구 목적 (Research Use Only, RUO) 으로만 제공됩니다. 사업자등록번호: 494-86-03792 | 판매자번호: 노보진코리아유한회사 | 대표자명: 리휘시앙 | 사업자주소: 서울시 강서구 마곡동 779-1번지 뉴브클라우드힐스 BT-230, 231호, 07790 | 전화번호: 02-2038-8036
Novogene Korea
  • Novogene Korea
  • Genomics
    • Human Whole Genome Sequencing
    • Plant & Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant & Animal De novo Sequencing
    • Microbial De novo Sequencing
    • Amplicon Sequencing
    • Shotgun Metagenomics Sequencing
    Transcriptomics
    • mRNA Sequencing
    • Total RNA Sequencing
    • Full-Length Transcriptome Sequencing
    • Whole Transcriptome Sequencing
    • Small RNA Sequencing
    • Circular RNA Sequencing
    • Metatranscriptome Sequencing
    • Prokaryotic RNA Sequencing
    Single Cell & Spatial Omics
    • Single Cell Gene Expression
    • Single Cell Immune Profiling Sequencing
    • Single Cell Long Read Transcriptome
    • Visium HD Spatial Gene Expression
    • Stereo-Seq Spatial Gene Expression
    • Xenium In Situ Spatial Transcriptome
    Epigenomics
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Directed DNA Methylation Sequencing (DM-Seq) NEW
    • Reduced Representation Bisulfite Sequencing (RRBS)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)

    Premade Library

    • Sequencing Only (Illumina 플랫폼)
    • Sequencing Only (PacBio 플랫폼)
    Proteomics & Metabolomics
    • Olink Proteomics
    • Quantitative Proteomics (MS)
    • Untargeted Metabolomics (MS)
  • 프로모션프로모션
    • 플랫폼
    • 자동화 운송 플랫폼 (Falcon)
    • BI 분석툴 (NovoMagic)
    • Customer Service System (CSS)
    • 브로셔
    • 케이스 스터디
    • 웨비나
    • 블로그
    • 샘플준비 가이드라인
    • 커뮤니티
    • 암 연구
    • 면역 종양학
    • 농업
    • 환경
    • 식품
    • 인간 마이크로바이옴
    • 동물 & 식물 마이크로바이옴
    • 신약개발
    • 희귀 질환 연구
    • 회사소개
    • 글로벌 입지
    • 뉴스룸
    • 채용 정보
  • 문의하기문의하기
  1. Home
  2. Resources
  3. Blog
  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.

서비스서비스 menu

고객지원고객지원 menu

기업정보기업정보 menu

서비스
WGSDe novo SeqAmplicon SeqShotgun MetagenomeDM-SeqmRNA-SeqSingle Cell Gene ExpressionVisium HDXenium In SituOlinkUntargeted Metabolomics
고객지원
노보매직CSSFalcon 플랫폼
기업정보
회사소개글로벌 입지플랫폼뉴스룸채용 정보문의하기
LinkedInLinkedIn hoverYouTubeYouTube hoverXX hoverMetaMeta hoverInstagramInstagram hover
Copyright © 2026 Novogene Co., Ltd. All Rights Reserved. 노보진의 한국 내 모든 서비스는 연구 목적 (Research Use Only, RUO) 으로만 제공됩니다. 사업자등록번호: 494-86-03792 | 판매자번호: 노보진코리아유한회사 | 대표자명: 리휘시앙 | 사업자주소: 서울시 강서구 마곡동 779-1번지 뉴브클라우드힐스 BT-230, 231호, 07790 | 전화번호: 02-2038-8036
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