![]() Stranded RNA sequencing (depletion of ribosomal RNA) Whole exome or target genome sequencingĤ. We can provide the following NGS applications (from library preparation to FASTQ files):Ģ. ![]() With tunable output and high data quality, this instrument can be used for several NGS based applications such as targeted genome sequencing, metagenomics and small genome sequencing. This benchtop NGS machine is suitable to generate 15 Gb of output with 25 million reads and 2×300 bp read lengths. Mid-output flow cell (130 M single read, 260 M paired-end read) High-output flow cell (400 M single read, 800 M paired-end read) With tunable output and high data quality, this instrument is suitable for many NGS based applications. This NGS machine is suitable to sequence single or paired-end reads, and flow cells are available in configurations for high output and mid output. We offer NGS sequencing services on Illumina MiSeq or NextSeq 500 instruments. NGS is driving genomic and transcriptomic discoveries and enabling the future of personalized medicine. With its high throughput and speed, NGS enables researchers to carry out a wide variety of applications including gene expression profiling, detection of epigenetic changes and metagenome or whole genome sequencing. NGS is a high-throughput technology that enables rapid sequencing of various DNA or RNA samples. The Genomic Medicine and Bioinformatics Core Facility is hosted by the Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen.Īssociate professor, Head of the Core FacilityĪssistant research fellow, Genomics Unit coordinatorĪssistant professor, Bioinformatics Unit coordinatorĪssistant professor, Genomics trainings coordinatorĪssociate professor, Biobanking service coordinator Moreover, we deliver advice on experimental design, bioinformatics assistance and training. In addition, the Core Facility continues to offer a variety of traditional genomic methods, including Sanger sequencing and real-time quantitative PCR. We manage samples for genomic projects starting from quantitative and qualitative analysis of RNA/DNA up to next generation sequencing (NGS) and data analyses using various NGS platforms. Our genomic services are available to academic and commercial users. The Genomic Medicine and Bioinformatics Core Facility has provided genomic and transcriptomic services to the local and international scientific community for almost 20 years.
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