Alignment to GRCh38

Regular price €29.00 EUR

(Not compatible with WGL Longreads sequencing test)

  • FASTQ data aligned to the GRCh38 reference genome
  • GRCh38 is the most recent reference genome
  • Receive BAM files, CNVs, SVs, Indels and SNP aligned to the GRCh38 reference via download, with the possibility to access your data from anywhere
We use a cutting-edge form of technology that not even the most advanced hospitals can provide and that allows us to sequenced your entire DNA with unparalleled precision, instead of focusing on only small parts of the DNA. 
Our Sequencing Center is located in L'Aquila, Italy, and with its 900 square-meter fully dedicated to Whole Genome Sequencing is considered Europe's largest private NGS laboratory. 

We perform all our analysis internally and thanks to our high-throughput next generation sequencing (NGS) equipment we guarantee superior quality.

Your sample and data will stay in the European Union (also if you are a US resident) and is protected by the EU General Data Protection Regulation (GDPR). Our technology offers data protection improvements not required by law but considered best practices in the industry.