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advitam
Whole Genome Sequencing · 30× Coverage
Upload .FASTQ or .BAM to sequence a full human genome
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Base Pairs Sequenced
0
of 3.2 Gbp human genome
Genes Identified
0
of ~20,000 annotated
Variants Found
0
SNPs · Indels · SVs
Pathogenic Risks
0
ACMG class 4–5
Coverage Depth
30.0
×
Illumina NovaSeq 6000
Initializing pipeline
· chr
—
0.0%
3.2 Gbp
0