
S E Q U E G E N I C S

A fully automated cloud platform to detect Structural Variants and other complex types of variation
Go from DNA extraction to curated VCFs with minimal hands-on time
A simple-to-use and reliable cloud platform to detect complex traits
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Identification and fine mapping of structural variants
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Large and small INDELs
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Copy number variations
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Pseudogene discrimination
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Tandem Repeat Sequencing
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Resolving allele phasing
How does it work?
1
Send us your sample or upload your long-read NGS raw data
2
Manage your databases and launch your variant calling analyses
3
Query and download your data
SQG Workflow
Organize your raw sequencing data in biosamples and databases
Launch a variant calling job on one or multiple genes on any biosample or database
Query the output to look for variants of interest
Database_1
Biosample_1
raw_reads.bam.1
raw_reads.bam.2
Biosample_2
raw_reads.bam.1
Database_2
Biosample_1
raw_reads.bam.1
Biosample_2
raw_reads.bam.1
raw_reads.bam.2
Database_3
Biosample_1
raw_reads.bam.1

