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De Novo sequencing

De novo sequencing is used to sequence unknown genomes where there is no reference sequence available.
Using a combination of short and long insert sizes with mate pair libraries and long paired-end reads, we are able to offer assembly and scaffolding of contigs to build the final consensus sequence.
We offer library preparation with:

  • Nextera® DNA Sample Prep Kit
  • Nextera XT DNA Sample Prep Kit for small genomes (bacteria, archaea, viruses)
  • TruSeq® DNA PCR-Free Sample Prep Kit for reduced library bias and gaps
  • TruSeq® Nano DNA Sample Prep Kit for samples with limited available DNA
  • Nextera® Mate Pair Sample Prep Kit for mate pair libraries up to 12 kb

For further information please fill out the form or write to info@galseq.com.

Bioinformatic analysis

Bioinformatics analysis 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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Applications

applications

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About us

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.