High-quality whole-*ome sequencing plus bioinformatics with omics2view.consulting GbR

Benefit now from our exhaustive expertise in sequencing and take advantage of our bioinformatic services for whole-genome, whole-exome, capture, and amplicon data.

Whole-genome (re-)sequencing, Whole-exome sequencing, Amplicon sequencing

Our service includes mapping of sequences to a reference (re-sequencing data), calculation of quality metrics, base coverage, SNP calling, SNP type, SNP quality scores, amino acid change, transcript consequence, pathogenicity prediction, copy number variation and small InDels.

Data analysis of capture data
Our high-performing analysis pipelines facilitate identification of SNP and InDels in captured DNA sequences. If you are interested, please contact us.