Insect Nanopore full-length transcriptome sequencing is an advanced method that utilizes third-generation sequencing technology to study insect gene expression and transcript structure. This technology reads the sequence of individual nucleic acid molecules using nanopore proteins, enabling the direct acquisition of complete transcripts without the need for assembly.
Lifeasible specializes in the field of insect research, providing advanced technical support for research and development in this area. Our insect Nanopore full-length transcriptome sequencing service enables full-length transcriptome sequencing of insect samples, without interruption, and can directly read the full-length sequence of high-quality individual RNA molecules from the 5' end to the 3' end polyA tail. It can accurately identify alternative splicing (AS), alternative polyadenylation (APA), fusion genes, long non-coding RNAs (lncRNA), and their target genes that cannot be accurately identified by second-generation sequencing, while simultaneously performing quantitative analysis of genes and transcripts.
The Nanopore full-length transcriptome sequencing we provide offers a powerful tool for insect transcriptome research, providing more comprehensive and accurate transcript information to help researchers gain a deeper understanding of insect gene expression regulation and transcript structural variation.
| Sample processing and library construction | Support for insect sample diversity. We support the processing of insect samples at different developmental stages, from different tissues, and under different experimental conditions. RNA quality control. Ensure sample quality. Library construction. Use cDNA-PCR library construction, support Direct RNA/cDNA library construction, and directly obtain full-length transcripts. |
| Nanopore full-length transcript library construction and sequencing | Utilizing Nanopore long-read technology to obtain complete transcript structures. |
| Data quality control and preprocessing | Performing raw data filtering, full-length identification, and quality assessment, etc. |
| Transcript structure analysis | Alternative splicing identification. Precisely identify five types of splicing, including exon skipping and intron retention. Fusion gene detection. Directly identify gene fusion events based on long reads. Alternative polyadenylation (APA). Analyze the regulatory mechanisms of the 3' untranslated region. New transcript discovery. Supplement the insect genome annotation and discover new genes or isoforms. |
| Quantitative and functional analysis | Transcript quantification. Quantify gene or transcript expression based on full-length sequences. Differential expression analysis. Screen for differentially expressed genes or transcripts in combination with biological replicates. Functional annotation
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| Integrated analysis | Species without reference genomes. De novo construction of gene model sets as a reference for RNA-Seq quantification. Species with reference genomes. Correction of gene models and optimization of annotation. Multi-omics integration. Combining genomic and metabolomic data to analyze insect-specific pathways. |
Fig.2 Our experimental process. (Lifeasible)
Lifeasible is at the forefront of the industry in insect research services, offering a full range of Nanopore services from library construction and sequencing to structural analysis and quantitative validation. We focus on identifying transcript structural variations and exploring functional mechanisms, and address insect-specific issues through multi-omics integration. If you are interested, please feel free to contact us.