Transcriptomics 6 Gb/sample

Transcriptomics using next-generation sequencing (NGS) is a molecular biology technique that involves the sequencing and analysis of the complete set of RNA transcripts produced by a cell or tissue under specific conditions. NGS can generate millions of short reads from a single sample, which can be used to quantify and analyze the expression levels of transcripts and identify novel transcripts. The transcriptomics NGS workflow involves the extraction of RNA from a biological sample, followed by library preparation and sequencing using high-throughput sequencing technologies, such as MGI or Nanopore. The resulting sequence data can be aligned to a reference genome or assembled de novo to identify and quantify known and novel transcripts. Transcriptomics NGS has numerous applications in various fields of research, including developmental biology, cancer research, neuroscience, and immunology, among others. It can be used to identify differentially expressed genes, detect alternative splicing events, and investigate the molecular mechanisms underlying various biological processes and diseases. Transcriptomics NGS can also be used for biomarker discovery and drug target identification. By analyzing the transcriptome of cells or tissues under different conditions, researchers can identify potential targets for therapeutic intervention and develop new strategies for disease diagnosis and treatment. Transcriptomics NGS is a powerful tool for understanding the complexity of gene expression and regulation, providing insights into the molecular mechanisms underlying various biological processes and diseases.