Basic Service

Next Generation Sequencing 

NGS allow us to sequence DNA and RNA much more quickly and cheaply than the previously used Sanger sequencing, and as such have revolutionized the study of genomics, molecular biology, but also in variety of research areas such as, cancer genomics, RNA sequencing, and Epigenomic analysis. Our Quick Discovery service provides the right experimental design and optimal technology for sequence capture based on different NGS applications. Finally, our advanced bioinformatics analysis will guide your research smoothly from sample data to discovery. While other companies deliver massive amounts of NGS data in Excel or text file formats, we go much further with in-depth bioinformatics analysis and the delivery of analysis results in user project relevant context. 

  • Whole transcriptome sequencing (RNA-Seq)

  • Small RNA sequencing (miRNA-Seq)

  • Whole exome sequencing

  • Whole genome sequencing

  • Chromatin immunoprecipitation sequencing (ChIP-Seq)

Microarray Analysis 

Microarray assays large amounts of biological material using high-throughput screening miniaturized, multiplexed and parallel processing and detection methods. Microarray analysis are used in interpreting the data generated from experiments on DNA, RNA, and protein microarrays, which allow researchers to investigate the expression state of a large number of genes - in many cases, an organism's entire genome - in a single experiment. 

  • Gene expression profiling

  • SNP genotyping

  • Copy number variation analysis

  • Global methylation

  • ChIP-ChIP analysis

  • miRNA profiling

  • Advanced microarray data analysis

  • QRT-PCR confirmation

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