OncoLand is a sophisticated oncology-focused database designed to accelerate cancer research. Integrating published research and large consortium cancer datasets, robust data visualization and discovery tools, OncoLand saves you valuable time and resources in your pursuit for actionable discoveries.
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OmicSoft DiseaseLand is the disease-focused platform designed to help you harness thousands of disease-focused datasets to accelerate biological discovery. Bringing together robust data visualization and analytics tools, OmicSoft “Land” technology rapidly connects you to the most relevant insights. Explore gene expression data at the gene, transcript, and exon level, as well as whole-transcriptome analyses of differential expression. Every project in DiseaseLand is carefully curated and processed through common pipelines, allowing you to quickly find the most relevant results across projects. DiseaseLand saves you valuable time and resources, enabling you to focus on your research.
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It’s DNA Day! DNA Day marks two significant DNA-related milestones — the 1953 discovery of DNA’s double helix and the completion of the Human Genome Project in April 2003. The National Human Genome Research Institute honors the day with a focus on educational opportunities, collaborating with universities and organizations to help students, teachers, and the public learn more about genetics and genomics.
While celebrating two big markers of our knowledge of DNA on this day, this is also a great chance to pay our respects to the tireless efforts of scientists around the world who are deepening our understanding of DNA and disease. Recently, one of our principal genome scientists, Dr. Sohela Shah, PhD, made a significant contribution to DNA data interpretation by leading the team that presented the most accurate disease class prediction and causal variant identification for the Johns Hopkins Challenge at this years CAGI conference.
We’re celebrating DNA Day with a time-limited $1,000 discount on our hereditary disease solution - the bundle of Biomedical Genomics Workbench and Ingenuity Variant Analysis.
Happy DNA Day!
New, powerful bioinformatics tool: The RNA-Seq Explorer Solution
Today we announced our new RNA-Seq Explorer Solution — a powerful bioinformatics tool that combines Ingenuity® Pathway Analysis™ and Biomedical Genomics Workbench® to generate clear insights for research into improved cancer detection, diagnosis, and treatment. One of the most compelling benefits of the RNA-Seq Explorer Solution is that it allows you to focus on biology, giving you the tools to drive your research forward and to publish novel findings. It transforms raw data from liquid biopsies — one of the most promising new ways to detect and characterize cancer — into clear, accurate, actionable insights. Ultimately, we believe that a powerful bioinformatics-driven liquid biopsy solution like this one will vastly improve precision medicine and cancer management.
Principal Scientist Jean-Noel Billaud is presenting data from this new solution at AACR at our theater presentation on Tuesday, April 19, at 3:00 p.m. We hope you’ll come by to hear the finer points of our new RNA-Seq Explorer Solution. You’re of course also welcome to stop by our booth #741 for at chat.
Get the full overview of our activites at AACR.
For more details on the RNA-Seq Explorer Solution, please read the official press release below.
Press release
QIAGEN launches streamlined bioinformatics for RNA sequencing of liquid biopsies
RNA-seq Explorer Solution generates clear insights for cancer ‘omics’ analyses
Hilden, Germany, and Germantown, Maryland, April 14, 2016 – QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced introduction of its unique RNA-seq Explorer Solution, a bioinformatics-driven approach to analysis and interpretation of “omics” data from liquid biopsy-based research. RNA-seq Explorer Solution is a new tool which integrates Ingenuity® Pathway Analysis™ Biomedical Genomics Workbench® and other QIAGEN bioinformatics solutions to generate clear insights for research into improved detection, diagnosis and treatment of cancer. The solution will be demonstrated at the American Association for Cancer Research (AACR) Annual Meeting in New Orleans.
“The RNA-seq Explorer Solution provides the most powerful bioinformatics tool for the analysis and interpretation of RNA sequencing data from liquid biopsies, including from tumor-derived exosomes. Next-generation sequencing of liquid biopsies, one of the most promising new ways of detecting and characterizing cancer, demands the highest-accuracy tools to make sense of inherently noisy data,” said Dr. Laura Furmanski, Senior Vice President and head of QIAGEN’s Bioinformatics Business Area. “QIAGEN’s streamlined RNA solution transforms raw data from liquid biopsies into valuable insights – a significant milestone for liquid biopsy analysis of indications such as cancer. The best bioinformatics will drive progress in precision medicine and cancer management.”
Liquid biopsy is a non-invasive method using samples of body fluids such as blood to detect and profile diseases such as cancer at the earliest stage, resulting in more successful prognosis and treatment. One liquid biopsy approach extracts DNA or RNA from tumor-derived exosomes, tiny enclosures that circulate in body fluids. In an RNA-seq workflow, scientists analyze and interpret exosomal RNA to determine gene expression profiles, identifying regulatory networks and potential isoforms of biological significance.
RNA-seq Explorer Solution facilitates simple, accurate discovery and validation of biomarkers, enabling researchers to go from raw data in FASTQ format to significant insights that home in on the genetic drivers of cancer. The solution draws upon QIAGEN’s Ingenuity Pathway Analysis (IPA), an all-in-one, web-based software application that enables analysis, integration and understanding of expression data. IPA is backed by the expert-curated Ingenuity Knowledge Base of highly structured, detail-rich biological and chemical findings. RNA-seq Explorer Solution also integrates QIAGEN’s Biomedical Genomics Workbench, a comprehensive data analysis platform that offers end-to-end workflows and tools for the alignment, normalization and statistical analysis of NGS experimental results.
In addition to demonstrating of the new RNA-seq solution at its booth at the AACR meeting, QIAGEN Bioinformatics recently released a four-part webinar series; the company will also have a sustained presence at the event. Click here for more details.
Leadership in liquid biopsies
RNA-seq Explorer Solution complements QIAGEN’s industry-leading liquid biopsy portfolio, which is spanning sample technologies, assay technologies and bioinformatics. It includes gold-standard solutions for the extraction of cell-free, circulating nucleic acids (cfDNA), circulating tumor cells (CTCs), and exosomes. In partnership with pharmaceutical companies, QIAGEN is developing and commercializing the broadest portfolio of companion diagnostics based on liquid biopsies, including the therascreen EGFR RGQ Plasma PCR kit, the first ever CE-IVD-marked blood-based test to guide treatment decisions for solid tumors.
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 September 30, 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).
Living with a rare disease is often lonely and isolating for patients and caregivers alike. Through our work with researchers and medical teams, we’re acutely aware of the difficulties experienced by the rare disease community, which range from a lack of resources and research to the impact of the diseases themselves. With Rare Disease Day 2016 we want to salute those who work and live with disease and to shine a spotlight on this area of medical research, which is all too often overlooked.
$1,000 discount
Most rare diseases have a genetic cause, and we’re proud that our tools are helping scientists contribute to efforts to unravel these challenging diseases. In fact, we’ve bundled a few of our most powerful tools into the QIAGEN Bioinformatics Clinical Research Solution for NGS DNA applications, created for researchers to discover more insights and get publication-ready results faster — and in honor of Rare Disease Day, we’ve reduced the price by $1,000. The solution includes:
To learn more and get the discount, please email us.
Customer stories
There are so many remarkable new stories about finding answers to rare disease, and in the past year it’s been an honor for us to share some of them. In case you missed them, here’s a quick glimpse of just a few of the amazing discoveries made by our customers in the rare disease field:
We’re proud to support these scientists and so many others around the world who are making a real difference in the lives of people coping with rare disease.
