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SMRT Leiden Assembly Grant

Submit your unique plant or animal genome proposal for a chance to win free de novo assembly services on PacBio SMRT Sequencing data. See details below.

We are excited to participate in our partner, PacBio’s, annual SMRT Leiden Conference in Leiden, Netherlands from June 12th – 14th. This back to back conference will include the SMRT Scientific Symposium on June 12th & 13th, featuring presentations from key experts and opinion leaders sharing their scientific discoveries and latest achievements from a variety of fields. The SMRT Informatics Developers Conference will follow on June 14th, focused on developing and improving analysis tools for PacBio SMRT Sequencing data. Software developers and bioinformaticians will spend the day focused on advancing new and existing tools for de novo assembly, genome phasing, structural variation, base modifications and Iso-Seq analysis.

During the SMRT Informatics Developers Conference on June 14th, DNAnexus will be presenting “Evaluating haplotype phasing from FALCON Unzip” at 10:30am in the session titled “DE NOVO ASSEMBLY.” In this talk, we evaluate the performance of FALCON Unzip in forming phased haplotypes by assembling and phasing the genomes of an artificial human.  By examining SNP’s that are known to be unique to one of the parents, we show that FALCON Unzip is able to produce impressive phasing information requiring nothing more than a little additional time in the compute environment to process the data.

DNAnexus is also honored to be a sponsor of PacBio’s Leiden Conference by providing the “SMRT Leiden Grant powered by DNAnexus” offering free de novo assembly for the most unique plant or animal genome in the world. One lucky winner will be selected for DNAnexus de novo assembly services on PacBio SMRT Sequencing data. Participants can submit proposals on the SMRT Leiden Grant website, with information on organism type and its impact on the scientific community. Proposals should be approximately 250 words in length and the genome size up to 1.5 Gbp, (>1.5 Gbp will be considered under special circumstances). Please note de novo assembly services will only be applied to data generated through PacBio SMRT Sequencing and sequencing is not included in the SMRT Leiden Grant.

Deadline for submission is June 29th, and the winner will be announced the week of July 9th.

Requiring massive computational resources to assemble reads or run structural variation detection across datasets, genome assembly is made even more challenging due to high levels of genetic diversity, repetitive elements, and duplicated genomic regions. Our bioinformatics expertise and computational power enable the delivery of high quality results, leveraging multi-omics data and tools in a collaborative and secure ecosystem. You can learn more about our fast, accurate, and cost efficient reference-quality assembly services that enable complex genome assembly, structural variation analysis, and physical mapping to achieve complete and accurate views of all types of genomic variation on our de novo assembly website.

Questions about DNAnexus de novo assembly or the SMRT Leiden Grant? Email us!

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About DNAnexus

DNAnexus the leader in biomedical informatics and data management, has created the global network for genomics and other biomedical data, operating in 33 countries including North America, Europe, China, Australia, South America, and Africa. The secure, scalable, and collaborative DNAnexus Platform helps thousands of researchers across a spectrum of industries — biopharmaceutical, bioagricultural, sequencing services, clinical diagnostics, government, and research consortia — accelerate their genomics programs.

The DNAnexus team is made up of experts in computational biology and cloud computing who work with organizations to tackle some of the most exciting opportunities in human health, making it easier—and in many cases feasible—to work with genomic data. With DNAnexus, organizations can stay a step ahead in leveraging genomics to achieve their goals. The future of human health is in genomics. DNAnexus brings it all together.