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.
Our Genomic Panels
Choose a report's category:
Connective Tissue Report
$29.00
/
Ehlers-Danlos Syndrome Report
$29.00
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Cardiovascular Report
$29.00
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Gastroenterology Report
$29.00
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Dermatology Report
$29.00
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Hematology Report
$29.00
/
Circadian Report
$29.00
/
ACMG Report
$29.00
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Methylation Mechanisms Report
$29.00
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Pediatric Report
$29.00
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Neurology Report
$29.00
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Autoimmunity Report
$29.00
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Metabolic Report
$29.00
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Endocrinology Report
$29.00
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Autism Report
$29.00
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Hereditary Cancer Report
$29.00
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Oncology Report
$29.00
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Acute Hepatic Porphyria Report
$29.00
/
Our Certifications
