Discover our new platform for exploring highly-curated single-cell RNA-seq data 

Are you looking for highly curated single-cell (scRNA-seq) data to validate your latest results? Have you ever spent hours or days processing data from a publication only to find your gene of interest isn’t detected?  Maybe you’ve tried a single-cell portal but find it lacks critical metadata? 

Discover our new solution that makes single-cell data analysis easy while delivering deep and novel insights. We’ve extended our valuable QIAGEN OmicSoft DiseaseLand and OncoLand frameworks to enable rapid exploration of single-cell data, creating the new QIAGEN OmicSoft Single Cell Land. Our team of certified curators manually curated hundreds of single-cell projects generating thousands of precisely curated cell clusters. You can access millions of cells that are searchable using any one of our more than 70 metadata attributes. Compare across projects and easily find the data you are looking for. Then, export your findings graphically, tabularly or to an open data standard.  

The new QIAGEN OmicSoft Single Cell Land lets you: 

Learn more about how QIAGEN OmicSoft Single Cell Land can support your research. 

Request a trial to explore how this database of scRNA-seq datasets can dramatically facilitate and accelerate your single-cell genomics research. 

At the AGBT conference in Orlando we announced a new collaboration with 10x Genomics to co-market and co-develop NGS, single-cell biology, and bioinformatics solutions. We believe that 10x Genomics will be innovative collaborators in the advancement of human genetics, and our partnership will unfold in multiple phases.

The collaboration will include an investigation of the implementation of 10x Genomic’ GemCode technology with our GeneReader NGS system. And from a bioinformatics perspective, we’ll also look into enabling the processing and analysis of 10x Genomics’ “Linked-Reads” with our suite of bioinformatics solutions aiming to address the challenges of data analysis, interpretation, clinical decision-support, and reporting that rely on testing for long-range phasing and structural variants in genomics.

We are thrilled to collaborate with 10x Genomics, and we look forward to providing even more comprehensive solutions for our NGS customers.

For more information the collaboration, please read the official press release below.

 

Press release

QIAGEN and 10x Genomics to enter into co-marketing and co-development collaboration

Multi-phase collaboration to advance next-generation sequencing, single-cell biology, and bioinformatics Sample to Insight solutions

Orlando, Florida, February 9, 2016 QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced a collaboration with 10x Genomics to develop and promote comprehensive solutions for next-generation sequencing (NGS), single-cell biology and bioinformatics.

This collaboration includes:

“QIAGEN’s collaboration with 10x Genomics enables both companies to better serve its customers, helping them make groundbreaking advances in single-cell biology, bioinformatics and beyond,” said Peer Schatz, CEO of QIAGEN. “10x Genomics is recognized for delivering critical long-range sequence information that greatly expands the quality of genome research. This partnership will further the potential of each of our product lines while providing significant new capabilities to NGS researchers.”

“We welcome the opportunity to partner with QIAGEN, with their comprehensive offerings for genomic analysis, ranging from sample preparation technologies to bioinformatics solutions for the interpretation and analysis of genomic data,” said Serge Saxonov, 10x’s Chief Executive Officer. “Access to long-range sequence information is becoming the standard for obtaining the most comprehensive understanding of disease, and we expect this collaboration to allow our respective customers to gain valuable insights that have previously not been possible.”

10x Genomics’ GemCode Platform overcomes existing NGS limitations through a combination of microfluidics, chemistry and bioinformatics. The system is a unique molecular barcoding and analysis platform that consists of instrumentation, reagents and software to provide a complete approach for a broad range of applications, including single-cell transcriptomics and whole genome analysis.

About QIAGEN

QIAGEN N.V., a Netherlands-based holding company, is the leading global provider of Sample to Insight solutions to transform biological materials into valuable molecular insights. QIAGEN sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective molecular testing workflows. QIAGEN provides these workflows to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare), Applied Testing (forensics, veterinary testing and food safety), Pharma (pharmaceutical and biotechnology companies) and Academia (life sciences research). As of December 31, 2015, QIAGEN employed approximately 4,600 people in over 35 locations worldwide. Further information can be found at http://www.qiagen.com.

Certain of the statements contained in this news release may be considered forward-looking statements within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, and Section 21E of the U.S. Securities Exchange Act of 1934, as amended. To the extent that any of the statements contained herein relating to QIAGEN's products, markets, strategy or operating results, including without limitation its expected operating results, are forward-looking, such statements are based on current expectations and assumptions that involve a number of uncertainties and risks. Such uncertainties and risks include, but are not limited to, risks associated with management of growth and international operations (including the effects of currency fluctuations, regulatory processes and dependence on logistics), variability of operating results and allocations between customer classes, the commercial development of markets for our products in applied testing, personalized healthcare, clinical research, proteomics, women's health/HPV testing and nucleic acid-based molecular diagnostics; changing relationships with customers, suppliers and strategic partners; competition; rapid or unexpected changes in technologies; fluctuations in demand for QIAGEN's products (including fluctuations due to general economic conditions, the level and timing of customers' funding, budgets and other factors); our ability to obtain regulatory approval of our products; difficulties in successfully adapting QIAGEN's products to integrated solutions and producing such products; the ability of QIAGEN to identify and develop new products and to differentiate and protect our products from competitors' products; market acceptance of QIAGEN's new products, the consummation of acquisitions, and the integration of acquired technologies and businesses. For further information, please refer to the discussions in reports that QIAGEN has filed with, or furnished to, the U.S. Securities and Exchange Commission (SEC).

 

Sample to Insight
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