Alignment to the GRCh38
$29.00
/
Whole Genome Sequencing 30X
(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.
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