COST OF CLC GENOMICS WORKBENCH UPDATE
COST OF CLC GENOMICS WORKBENCH FULL
COST OF CLC GENOMICS WORKBENCH SOFTWARE

COST OF CLC GENOMICS WORKBENCH FULL

What’s more, you’ll enjoy full flexibility. This is made possible via QIAGEN CLC LightSpeed Module, which enables an ultra-fast and accurate FASTQ to VCF pipeline for hereditary germline mutation analysis.

COST OF CLC GENOMICS WORKBENCH SOFTWARE

Our all-in-one NGS bioinformatics software QIAGEN CLC Genomics Workbench Premium now offers you a faster, more accurate, more flexible and more affordable way to process WGS and WES files in bulk. What if there were a scalable, point-and-click solution that could handle all your WGS, WES and large panel data analysis needs without having to purchase vast amounts of specialized infrastructure? A software that could run with a GUI and be used by anyone with minimal training ? What if you didn’t have to compromise between speed and quality? Introducing a better, faster, cheaper and more flexible tool for WGS and WES analyses More investment in your bioinformatics infrastructure? Nope-now you don’t have to How do you keep costs down yet deliver quality results with quick turnaround in a world of shrinking budgets? The requirement for fast and consistent turnaround times, also at peak demand, can quickly translate into a need for more personnel, more processing power-and more investment. Many high-speed NGS analysis solutions require purchasing expensive, highly specialized hardware, massive computers or large cloud computing contracts. Your customers, as well as your business, depend on it. Whether you run a genome center, testing facility, core lab or provide sequencing services, you’ve got to deliver variant call files (VCFs) at an unbeatable price and with consistent quality and turnaround time, even at peak demand. However, the total cost of ownership associated with bioinformatic analysis of the resulting files remains a bottleneck. With new machines and chemistries, the cost of sequencing has decreased significantly. QIAGEN Digital Insights’ licensing models enable laboratories to analyze WGS and WES samples in parallel.It’s exciting that advancements in high-throughput sequencing techniques and analysis enable us to generate whole genome (WGS) and whole exome (WES) data in bulk for many species, including humans. The quicker unwanted mutations are spotted, the sooner associated diseases can be identified and treated.” “Its cost and time efficiency gives high-throughput NGS sequencing laboratories the chance to use the technology widely for clinical and research clients. “LightSpeed will allow QDI to maintain its leadership position in data analysis as the market moves away from analyzing a few hundred selected genes to comprehensive genetic testing,” says Sheldon.

This enhancement in CLC Genomics secondary analysis software demonstrates QIAGEN’s continued leadership and commitment to targeted growth areas, including WGS and WES. QIAGEN Digital Insights’ investment in the LightSpeed technology is ideally suited to NGS areas such as neonatal screening for hereditary diseases or large population-genomics studies in which speed and cost are priorities. “Thanks to LightSpeed’s ground-breaking technology, WGS analysis is extremely fast, beats most other FASTQ to VCF workflows on accuracy, uses less power and requires no investments in new hardware or software licenses beyond CLC.” “QIAGEN CLC Genomics Workbench Premium is much faster, more accurate, greener and cheaper than previous data-analysis and visualization solutions,” says Jonathan Sheldon, PhD, senior vice president of QIAGEN Digital Insights. Alternatively, labs can efficiently run the QIAGEN CLC LightSpeed technology on existing local hardware with similar performance. With QIAGEN CLC LightSpeed software accelerator technology, labs can run WGS analyses for about $1 per genome and WES for less than a few cents per exome using cloud infrastructure, the company says. It can analyze an entire human genome at 34x coverage on an ordinary computer in just 25 minutes and a 50x whole exome in 90 seconds within standard cloud environments.

COST OF CLC GENOMICS WORKBENCH UPDATE

The update to QIAGEN CLC Genomics Workbench Premium incorporates a software accelerator that converts raw sequencing data in FASTQ files from any paired-end short read sequencing platform into interpretable lists of genetic variants in the VCF format. QIAGEN Digital Insights (QDI), the bioinformatics business of QIAGEN, unveiled their enhanced QIAGEN CLC Genomics Workbench Premium that removes the data-analysis bottleneck of next-generation sequencing (NGS) via improved analysis speed to help analyze and interpret whole genome sequencing (WGS), whole exome sequencing (WES), and large panel sequencing data.

Cost of clc genomics workbench