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RNA sequencing (RNA-Seq) harnesses the capabilities of high-throughput sequencing methods to give you a better understanding of the transcriptome of cells. The sequencing data will facilitate the discovery of novel transcript, identification of alternatively spliced genes, and detection of allele-specific expression. Eurofins Genomics offers end-to-end RNA-Seq solutions for a wide range of biological samples, using both Illumina and PacBio platforms. Our experienced team works closely with you to design a customised workflow tailored to the specific objectives of your project.
We offer a range of transcriptome sequencing services tailored to different research needs. A variety of library preparation options are available for each application, enabling data generation that aligns with your specific project requirements.
Our transcriptome sequencing services include:
Identify the genes present in your transcriptome
De novo transcriptome sequencing provides a comprehensive analysis of expressed genes at a specific time point and under a defined physiological condition. Multiple sequencing reads are generated from each transcript and subsequently assembled to reconstruct the corresponding transcripts or unigenes. The libraries are sequenced using Illumina NextSeq/NovaSeq platforms. In addition, PacBio and Oxford Nanopore long-read sequencing can be performed to obtain full-length transcript sequences. Eurofins Genomics has developed a proprietary bioinformatics pipeline for the de novo assembly of short Illumina reads and long-read full-length transcripts, enabling accurate and cost-effective reconstruction of transcripts.
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Analyse gene expression responses and rely on our long-term experience
mRNA sequencing (mRNA-Seq) is widely used for gene expression analysis and the detection of alternative splicing events. Our RNA-Seq services provide a comprehensive view of all expressed transcripts within your sample. By capturing the entire transcriptome through high-throughput sequencing, RNA-Seq enables the identification of novel transcripts, novel isoforms, alternative splice variants, rare transcripts, and single nucleotide polymorphisms (SNPs)
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