Next Generation Sequencing (NGS) technologies are revolutionizing biology (video). But analyzing NGS data requires dedicated bioinformatics specialists who are not available in most labs. Data2Bio™ can help you overcome the challenges of analyzing increasingly large and complex NGS data sets. Members of our team were early adopters of NGS technologies and have been analyzing NGS data ever since. We can help you design, conduct, analyze, and interpret a wide variety of NGS experiments from data generated by Illumina and Life Technology instruments.

Overview of tGBS - Genotyping by Sequencing on Ion Proton™ System In-depth description of tGBS - tGBS™: A Next Generation Genotyping-by-Sequencing Technology

NGSeasy™ Services

RNA-seq experiments to discover differentially expressed genes.
Genome and transcriptome resequencing to discover genetic variants (i.e., SNPs)
Assemble paired-end transcripts into contigs.
Gene mapping via Bulked Segregant RNA-Seq (BSR-Seq) service.
tGBS™ efficiently genotypes mapping populations and diversity panels
FSR to identify sequences flanking T-DNA insertions (or transposons)
Sequence and Assemble genomes with the accuracy of a BAC-by-BAC approach and the efficiency of NGS.
Describe your requirements and we will design an experiment.

Our genomics and bioinformatics services allow you to focus on the biology. We can generate NGS data for you or work directly with your sequencing facility to download your data to our servers, conduct the analyses and then report the results to you. We can even provide publishable figures and text describing the methods used to analyze your NGS data that can be inserted into your manuscripts.