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Sequencing.com

Custom Genome Analysis Interpretation Services | Bioinformatics Pipelines

Fully-automated cloud-based bioinformatics pipelines for genome sequencing analysis customized for laboratory partners.

Purchase for $30.00  

Get 100% of your DNA data with Whole Genome Sequencing.

Buy A Kit

Already have data from a DNA test? Upload your data for free.

Custom-Ordered, Fully Automated Bioinformatics Pipeline for Genome Sequencing Analysis

Whole Exome (WES) and Whole Genome (WGS) Data processing service including:

  • Secure Data Import
  • Data Quality Control Checks
  • Pre-Processing
  • Primary Analysis
    • Alignment
    • Telomere Length
    • Methylation
  • Secondary Analysis
    • SNV calling
    • DIV (INDEL) calling
    • SV (Structural Variant) calling
    • CNV (Copy Number Variation) calling
    • Mitochondrial Heteroplasmy
    • HLA Typing
  • Annotations
  • Tertiary Analysis
    • Phenotype Interpretation
    • Report Generation
    • Seamless, automated processing with any app from ourDNA App Store
      • The world's largest marketplace of tertiary analysis apps including health, wellness, nutrition, fitness, genealogy/ancestry, rare diseases, pharmacogenomics and more.
  • Confidential, HIPAA-compliant Data Storage
    • fastq, bam, sam, cram, genome vcf (gVCF), clinical+ vcf and regularvcf
  • Online, secure delivery of data files, interpretation (genetic reports) and app results to the laboratory's customers

 

Whole Genome Sequencing and Genotyping Array Add-On Service

We also provide end-to-end solutions that include worldwide shipping of DNA collection kits for ourUltimate Genome Sequencing service, which includes30x whole genome sequencing starting at $399 before quantity discounts. This service provides data on all types of genetic variations including SNPs, INDELs, SVs, CNVs, mitochondrial heteroplasmy, HLA typing, and telomere length.

If you're looking for a more affordable option, ourUltimate DNA Test includes an advanced genotyping microarray that provides data on around 30 million variants (SNPs and INDELs). 

Additional information about both tests can be foundhere.

 

Third-Party Raw DNA Data Analysis

Custom bioinformatics pipelines are also available for importing, processing and interpretation of third-party raw DNA data, such as from direct-to-consumer (DTC) companies. This includes 23andMe, Ancestry,MyHeritage, and FamilyTreeDNA. 

Compatible with 20+ DNA Tests

This app analyzes data from other DNA tests & genome sequencing services including 23andMe, Ancestry, MyHeritage and more.

Upload My Data

Learn More About Your DNA & Health

Read about the latest advancements and discoveries that may be relevant to your DNA and health on our DNA Education pages. We add new articles based on published genetic research every week.

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