Next Generation Sequencing

ArrayGen offers Next Generation Sequencing Contract Research Service Laboratories. In accordance with research and publication standards, we offer comprehensive sample data analysis as well as custom-based complicated analysis. We offer a broad range of NGS applications, including transcriptome profiling, miRNASeq, whole genome or exome analysis, and more. Along with real-time raw dataset processing and industry-based training, we also offer help up till publication standards figures and tables.


ArrayGen provides an array of NGS Data Analysis services from different trnascriptome platform (illumina, 454, SOLID, Ion-Torrent, PacBio, Nanopores etc) including

  • De novo genome and transcriptome assembly
  • Genome alignment and analysis
  • Chip-Seq Analysis
  • Methylome-Seq Analysis
  • Reference Based RNA-Seq Analysis
  • De-novo Based RNA-Seq Analysis
  • MicroRNA-Seq Analysis
  • Targeted re-sequencing (Exome-Seq) Analysis
  • DNA-Seq (Genome variant Detection) Analysis
  • Mapping, Annotation and Comparative Genomics Analysis (CGA)
  • 16S/28S/ITS rRNA Metagenomic Analysis
  • Metatranscriptome Analysis
  • Custom Arrays for NGS Data validation

Customized data analyses are available upon request as well as all different publication report generation as per the client request. We do support with all genomics algorithm development and implementation of same as per the client interest.

We have different hands on training modules and clients can get their data analysed as well as training on complete analysis pipeline with their own datasets. Please visit at https://www.arraygen.com/workshop-training.php know more details.


For further enquiry please contact us or write to us at info@arraygen.com.