INVIEW™ HUMAN EXOME by GATC Biotech

Manufacturer GATC Biotech  |  Available Worldwide
4.8
/
5.0
  |  3 reviews
Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol for low-input samples (≥ 10ng) Available under diagnostics standard (ISO17025) INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications. Exome enrichment with the latest Agilent SureSelect chemistry and massively parallel sequencing of the coding regions i... Read more


INVIEW™ HUMAN EXOME by GATC Biotech product image
INVIEW™ HUMAN EXOME

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Average Rating: 4.8
3 Scientists have reviewed this product

5 out of 5
Ease of use
5 out of 5
After sales service
5 out of 5
Value for money


  • Status:

    Reviewer
  • Member since: 2017

  • Organization: university of Turku



  • Ease of use
    5 out of 5
    After sales service
    4 out of 5
    Value for money
    4 out of 5
Good service
Rating: 4.3

  • Application Area: identify genetic alterations

"Fast service, good quality and a good bioinformatic service too"

Review date: 18 Jul 2017 | INVIEW™ HUMAN EXOME
  • Status:

    Reviewer

  • Member since: 2017

  • Organization: CGPP-IBMC, i3S



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
Quality results, great customer care
Rating: 5.0

  • Application Area:Analysing genetic variation in human patients

"GATC Biotech's INVIEW™ HUMAN EXOME is a great service for sequencing of the human genome protein-coding regions. We've been using it for the past year or so, having sequenced about 500 samples, and quality has been great: we consistently get the 30x (or multiples of) promised on-target coverage using the latest Agilent SureSelect Human All Exon V6. Using their myGATC web portal, we can follow all steps of the sequencing process from sample reception to results availability, including flagging samples that failed QC. Overall, very happy with the quality, reproducibility and turn-around time."

Review date: 17 Jul 2017 | INVIEW™ HUMAN EXOME
  • Status:

    Reviewer

  • Member since: 2016

  • Organization: Neuromuscular Research Dept. (Medical University of Vienna)



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
Great service and top data quality!
Rating: 5.0

  • Application Area:clinical whole-exome sequencing

"Based on more than 3 years of experience, it can be stated that GATC delivers top quality human exome sequencing data in only 2-3 weeks. Raw sequencing data (fastq files) are fed into our own bioinformatics pipeline and routinely produce high quality datasets for downstream analysis in variant calling and mutation detection. This holds true for 99% of more than 200 datasets! The extremely high reproducibility in library preparation and enrichment allows detecting intragenic deletions and duplications through comparative coverage analyses. People involve in customer care at GATC maintain highly professional, competent and friendly service. GATC's exome sequencing service can be highly recommended!"

Review date: 26 Feb 2016 | INVIEW™ HUMAN EXOME

Highlights:

  • Fastest exome sequencing, starting from one sample
  • Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample)
  • Special protocol for low-input samples (≥ 10ng)
  • Available under diagnostics standard (ISO17025)

INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications.

Exome enrichment with the latest Agilent SureSelect chemistry and massively parallel sequencing of the coding regions is a versatile and economic tool for researchers who want to identify relevant disease-causing mutations.  Customers have the option to complement their BioIT analysis with the established QIAGEN Ingenuity Variant Analysis software. INVIEW HUMAN EXOME EXPLORE is ideal for studies on germline mutaitons, whereas INVIEW HUMAN EXOME ADVANCE is perfectly suited to investigations of both germline and somatic mutations. INVIEW™ HUMAN EXOME is a highly standardised complete solution for clinical and medical researchers to help them answer important questions faster.