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.

[Read More]

[Read More]

The team at GalSeq has NGS experience dating back from 2009.
We initially worked on an Illumina Genome Analyzer IIx, and then moved to the new HiSeq 2500 and HiSeq 4000.
The building blocks of our bioinformatic pipeline, such as FusionAnalyser, CEQer and SpliceFinder, have been downloaded by thousands of researchers.