NGS Data Analysis

ArrayGen offers a range of Next Generation Sequencing (NGS) data analysis for disease association studies, cancer genomics, personalized medicine, agriculture biotechnology and life sciences to help researchers derive meaningful conclusions from their data. We are a team of data analysis experts, bioinformatics tool developers, and life scientists determined to simplify, enhance, and innovate the analysis of genomes.

ArrayGen provides an array of NGS Data Analysis services from different sequencing 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 know more details.

For further enquiry please contact us or write to us at
Request for Custom Array Design