Alignment to the GRCh38

Regular price $29.00
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(Not compatible with WGL Longreads sequencing test)

  • FASTQ data aligned to the reference genome GRCh38 ;
  • GRCh38 is the last genome version release;
  • Receive BAM files, CNVs, SVs, Indels and SNP aligned to the reference GRCh38 via cloud, with the possibility to access your data from anywhere.