Celemics signs an agreement to supply BTSeq™ to Sangon Biotech Co., Ltd., a Chinese genetic analysis company

Celemics signs a supply agreement for BTSeq™ solution with Chinese Sanger sequencing service company

Celemics, South Dakota State University, announce partnership for the development of Hybridization NGS-based Multiple Swine Pathogen Co-Detection Panel

Celemics, Strand Life Sciences Partner on Integrated Platform for NGS Analysis

Celemics: Not All NGS Companies Are the Same
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BRCA 1,2 Panel

Comprehensive and Accurate Analysis of BRCA 1,2 Genes

Qualified with Clinical Grade Performance

Overview

Celemics’ BRCA 1,2 Target Enrichment Panel is designed to enrich
whole coding sequences (CDS) of the BRCA1 and BRCA2 genes
including UTR, promoter, and +/- 40 bases of CDS to detect
the variants in the splicing site.

Using Celemics‘ BRCA 1,2 Panel customers can obtain information on all types
of variants including large indel and CNV. High performance of the panel guarantees reliable and consistent sequencing results
to customers even if using DNA from low-quality clinical samples or FFPE. Additionally, Celemics provides clinical-grade reports from our proprietary bioinformatics
pipeline and in conjunction with Strand Life Sciences.
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Features &
Benefits

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    Targets the whole CDS (+/- 40) and promoter regions of
    BRCA 1,2 with high specificity
    Target regions not only cover CDS regions, but are expanded by ±40 of CDS
    to detect splicing site variants.
    Probes specifically designed for detecting deletion, duplication,
    and large rearrangement
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    Compatible with a variety of sample types
    No compromise on panel performance regardless of specimen types, even
    for challenging ones such as blood or FFPE
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    Market leading panel performance in uniformity and coverage
    Designed to target the whole exon regions of BRCA 1, 2 gene with 100%
    coverage (RefSeq) and validated to yield 100% coverage
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    Clinical grade performance
    CE-IVD certified target enrichment panel
    Greater than 95% sensitivity and 99.5% specificity
    for all types of mutations (SNV and Indel)
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    Provision of Bioinformatics SW
    FASTQ to annotated VCF
    Clinical grade report
    EU-GDPR compliant through usage of Europe-based server

Performance

Market leading panel performance in Uniformity and Coverage Comparison data with competitors' products

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  • The extremely low standard deviation of uniformity enables consistent and reliable sequencing results
  • In-house test of the panel shows 100% of coverage for all target regions including whole CDS (+/- 40 bp), UTR, and promoter region

User-friendly analysis report with information of all types of variants and CNV

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  • The extremely low standard deviation of uniformity enables consistent and reliable sequencing results
  • In-house testing of the panel indicated 100% coverage for all target regions including whole CDS (±40 bp), UTR, and promoter region

Applications

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    Breast and Ovarian cancer related fields

Resources