• Just like a chameleon utilizing its
    colored pigments and crystals to
    adapt to its surroundings,
    we proactively pioneer and adapt to
    the everchanging NGS markets with
    our cutting-edge technology to
    support our customer’s needs.

Celemics Whole Exome Sequencing Service

Ultimate Exonic Coverage · Customizable Bioinformatics

Overview

Celemics Whole Exome Sequencing Service is a
comprehensive solution that covers all target regions of
major WES panels available in the market.

With the target size of 37 Mb, our WES service does not compromise on performance in
terms of coverage and uniformity, enabling highly efficient and cost-effective solutions to
your WES service needs.

Our WES Service is also supported by Celemics Analysis Service (CAS), an end-to-end
bioinformatics solution.

Celemics WES Service

  • T2 Exome
  • T Exome
  • I Exome
  • A Exome
Encompassing all target regions of major WES panels in the market.

Features &
Benefits

Complete Whole Exome Coverage
Covering exonic regions of major exome panels (37 Mb) with
>98% coverage.
FASTQ to Clinical Interpretation Support
Experience our full bioinformatics support
and customization service
Superior Performance in the Market
Strong capture performance against GC-rich regions as well
as higher quality in coverage and uniformity.

Bioinformatics
Support

CAS  (Celemics Analysis Service) Workflow

    • NGS Data [FASTQ]
    • Alignment
    • Variant
      Calling
    Primary
    Analysis
    BAM, VCF
  • Secondary
    Analysis
    Annotated VCF, CNV,
    Large InDel, Fusion,
    TMB, MSI
    • Variant
      Prioritization
      and Preclassi
      fication
    • Clinical
      Interpretation
      and
      Reporting
    Tertiary
    Analysis
    Clinical interpretation,
    Visualization, Heatmap,
    Phylogeny, etc.
  1. Analysis Option

  2. Output

  3. Analysis Step

Clinical Report Example : Includes pathogenicity and drug associated information

Specification

Specification
Target size 37 Mb
Covered region CCDS, RefSeq, Gencode
Sample types Genomic DNA, Cell-free DNA, FFPE, Fresh frozen tissue*
Sequencing depth Standard: 100x
Turnaround time Standard: within 6 weeks
Deliverables
  • 1. Primary Analysis: FASTQ to annotated VCF
  • 2. Secondary Analysis: CNV, Large InDel, TMB&MSI
  • 3. Tertiary Analysis: Clinical interpretation
  • 4. Visualization curation: Heatmap, CNV visualization, statistical analysis, etc.
Note: please contact us for the following information:

* Sample amount for different sample type

More options for sequencing depth

Faster turnaround time