GalSeq offers a complete bioinformatic analysis using both available web tools and in-house developed bioinformatics tools, such as FusionAnalyser, for fusion detection in RNA-Seq experiments, and CEQer, to study copy number and allelic imbalance abnormalities in matched exome sequencing.

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GalSeq has been created by a team of scientists with a strong experience in Next Generation Sequencing (NGS) and in Bioinformatics.
Galseq offers NGS services on Illumina platform, from design, to library preparation, to data analysis with completely customizable software.