Regulatory agencies increasingly demand detailed characterization of transgenic cell lines or organisms that produce biological products. We will de novo assemble and correct the genome sequence of the cell line to meet that demand.
Contact usWith our extensive knowledge we can offer solutions that cover the whole process of going from a biological sample to a complete genome sequence and annotation. With our in house developed tools we can do that for even the largest genomes.
To get the most out of your genome assembly annotation of genomic features is important. We use various tools to annotate the genome and we can also generate the full length transcript data that allow for even better gene models.
Regulatory agencies increasingly demand detailed characterization of transgenic cell lines or organisms that produce biological products. We will de novo assemble and correct the genome sequence of the cell line to meet that demand.
Future Genomics Technologies, founded in 2017, is a collaboration between biotech company BaseClear and Leiden University. We work closely together with Oxford Nanopore Technologies and use their revolutionary nanopore sequencing platforms to develop new genomics applications. We are one of the world’s first Oxford Nanopore Technologies certified sequencing providers. Our customers include biotechnological and (bio)pharmaceutical companies, academic and research institutes, as well as agro- and food industries.
Future Genomics Technologies uses the latest Next Generation sequencing technologies, including those of Oxford Nanopore Technologies and Illumina. Next generation sequencing has completely revolutionized the way in which complex genetic information is being unraveled.
More infoContact usWe employed nanopore sequencing technology and a new bioinformatics tool called TULIP to sequence and assemble the European …
(Ophiophagus hannah) June 24, 2020 We’ve sequenced the genome of the largest venomous snake with short reads and …
As proof of principle that a complex yeast genome can be resolved much better using long read sequencing …
