Member since: 2017
Organization: university of Turku
Application Area: identify genetic alterations
"Fast service, good quality and a good bioinformatic service too"
Member since: 2017
Organization: CGPP-IBMC, i3S
Quality results, great customer care
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."
Member since: 2016
Organization: Neuromuscular Research Dept. (Medical University of Vienna)
Great service and top data quality!
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!"
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.