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Whole Genome Sequencing

Whole genome sequencing allows researchers to investigate through the entire genome sequence and discover also variants that lie outside the coding regions.
Although most of the known disease-causing variants are located in the coding regions and can be detected by exome sequencing, with whole genome sequencing you can investigate also regulatory regions like promoters, enhancers and silencers where alterations can affect gene activity and protein production.
Whole genome sequencing can also be useful to characterize complex structural variations of the genome.
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.