Next Generation Sequencing (NGS) involves massively parallel sequencing of millions of DNA fragments, providing large amounts of data quickly and at an affordable cost. NGS technology is revolutionizing life sciences research and healthcare. The speed, throughput and flexibility of NGS provide researchers with the means to gain valuable insights at an unprecedented rate. No longer used for purely academic research, NGS technology is now spreading to clinical applications and helping to improve our understanding of the disease.
Although recent technological developments have made NGS more accessible to smaller laboratories, there are still many obstacles to adopting it. The high costs, fragmented workflows and the complexity of data analysis and interpretation make it challenging. There is an urgent need for a simpler, more cost-effective and efficient way for labs to take advantage of NGS technology and improve the outcomes. Creative Bioarray provides comprehensive and end-to-end NGS services including nucleic acid isolation, library preparation, sequencing and data analysis tailored to your needs. All of our sequencing offerings are executed on the latest NGS instrumentation with the rapid turnaround times.
Our NGS services include but are not limited to:
- Whole Genome Sequencing
- Targeted Re-sequencing
- Exome Sequencing (Exome-Seq)
- Transcriptome Sequencing
- Genome Methylation Sequencing
- Amplicon Sequencing
- RNA Sequencing (RNA-Seq)
- CRISPR Validation
- Epigenomics
- Metagenomics
Key Features of Our NGS Services
- All genomics solution under one roof
- Highly experienced and qualified personnel
- Fast turnaround time
- Competitive price
- State-of-the-art instruments and cutting-edge technologies
- Rigorous quality control
- Personalized NGS and customized bioinformatics solution to suit your research needs
