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AI-Supported Genetic Data Analysis Platform

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RNA Transcriptome Sequencing

Pairend NGS Cloud > Next-Generation Sequencing > RNA Transcriptome Sequencing

What is RNA Transcriptome Sequencing?

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RNA Transcriptome Sequencing (RNA-Seq) is an advanced technology that allows for highly precise analysis of gene expression in cells. This method is used to understand which genes are actively expressed in an organism or a group of cells at a given time. It plays a crucial role in genetic research, biomedical studies, and the biotechnology sector.

RNA-Seq is used in gene expression analysis, alternative splicing studies, mutation and SNP detection, non-coding RNA discovery, and disease research. It is particularly valuable for identifying genetic changes and discovering biomarkers in diseases such as cancer.

Advantages

  • High Precision & Reliability: Obtain detailed and accurate data with next-generation sequencing technologies.

  • Comprehensive Data Analysis: We provide not only gene expression profiles but also additional insights such as alternative splicing events, gene fusions, and SNPs.

  • Fast and Efficient Results: Our optimized processes ensure quick results from sample collection to result reporting.

  • Customized Solutions: We offer data analysis and reporting services tailored to your needs.

Health, Research, and Personalized Genetic Solutions

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All Your Questions Answered About Our RNA-Seq Service!

RNA transcriptome sequencing is a technique that determines which parts of an organism’s genetic information are active and which genes are being expressed. RNA is a molecule synthesized from DNA that carries genetic information inside cells. RNA transcriptome sequencing helps us understand cellular activity and gene expression by examining all RNA molecules. This enables in-depth analysis of biological processes, diseases, and genetic differences.

RNA transcriptome sequencing provides the following essential data:
✔️ Gene Expression Profiling: We determine which genes are active and how much they are expressed.
✔️ Alternative Splicing: We discover different forms of genes that contribute to genetic diversity.
✔️ Expression of Different Cell Types: We analyze the differences in gene expression between various cell types.
✔️ Biological and Disease Processes: We uncover the molecular basis of diseases through gene expression.

RNA transcriptome sequencing is widely used in various biological and clinical fields:
✔️ Cancer Research: We analyze the genetic expressions of cancer cells to discover new treatment targets.
✔️ Biomarker Development: We can develop biomarkers for early disease diagnosis.
✔️ Drug Development: We examine the effects of drugs on gene expression to optimize treatment processes.
✔️ Neurological Disorders: We investigate the molecular impacts of diseases like Alzheimer’s and Parkinson’s.
✔️ Hereditary Genetic Disorders: We explore the mechanisms of genetic diseases to find potential treatment avenues.

RNA transcriptome sequencing results are typically obtained within 4 to 8 weeks. After sample collection, RNA extraction, sequencing, data analysis, and bioinformatics interpretation take time. Quality control processes are implemented at each step to ensure the accuracy and meaningfulness of the results.

RNA transcriptome sequencing results are typically delivered in the following formats:
✔️ FASTQ: Raw sequencing data
✔️ BAM: Mapped sequencing data
✔️ GTF/GFF: Files showing the location and structure of genetic features
✔️ Gene Expression Data: Data related to gene expression levels
Additionally, bioinformatics analysis reports and interpretations are provided.

RNA transcriptome sequencing provides high accuracy in determining gene expression, but the clinical significance of the results may vary depending on biological context and genetic factors. Genetic counseling and clinical evaluation are recommended for more accurate interpretation of the results.

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