Alignment to the GRCh38
$34.99
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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.
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$34.99
(+$5.99)