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NGS Data Analysis Service
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.
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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