TY  - JOUR
A1  - Wolf, Beat
A1  - Kuonen, Pierre
A1  - Dandekar, Thomas
A1  - Atlan, David
T1  - DNAseq workflow in a diagnostic context and an example of a user friendly implementation
T2  - BioMed Research International
N2  - Over recent years next generation sequencing (NGS) technologies evolved from costly tools used by very few, to a much more accessible and economically viable technology. Through this recently gained popularity, its use-cases expanded from research environments into clinical settings. But the technical know-how and infrastructure required to analyze the data remain an obstacle for a wider adoption of this technology, especially in smaller laboratories. We present GensearchNGS, a commercial DNAseq software suite distributed by Phenosystems SA. The focus of GensearchNGS is the optimal usage of already existing infrastructure, while keeping its use simple. This is achieved through the integration of existing tools in a comprehensive software environment, as well as custom algorithms developed with the restrictions of limited infrastructures in mind. This includes the possibility to connect multiple computers to speed up computing intensive parts of the analysis such as sequence alignments. We present a typical DNAseq workflow for NGS data analysis and the approach GensearchNGS takes to implement it. The presented workflow goes from raw data quality control to the final variant report. This includes features such as gene panels and the integration of online databases, like Ensembl for annotations or Cafe Variome for variant sharing.
KW  - next generation sequencing
KW  - genome browser
KW  - mutation
KW  - algorithm
KW  - database
KW  - format
KW  - discovery
KW  - exome
KW  - variants
KW  - alignment
Y1  - 2015
UR  - https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/14452
UR  - https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-144527
IS  - 403497
ER  -