Goldenhelix.com Website Review

we provide a complete, end-to-end solution for clinical labs and hospitals to an*lyze next-generation sequencing data. our entire clinical pipeline consists of software products that are de*ply integrated with each other. in addition, we provide automation capabilities that are crucial in high-throughput testing environments. no per-sample charges! you will save money with our annual subscription model. licenses include unlimited training and support to snp & variation suite is a powerful an*lytic tool that allows biologists and other researchers to easily perform complex an*lyses varseq is an intuitive, integrated software solution for tertiary an*lysis. with varseq you can automate your workflows and an*lyze built on the same algorithms of varseq, vswarehouse is a scalable, multi-project warehouse for ngs variant call sets, clinical reports dr. benjamin darbro, director of shivanand r. patil cytogenetics and molecular laboratory dr. heather huson, professor of dairy cattle genetics, odyssey dna lab dr. hela azaiez, as*ociate research scientist, molecular otolaryngology and renal research laboratories ability to visualize results, all in one application. so when people say 'it costs money,' i say it's better to have one program that can. presented by: eli sward, ph.d, field application scientist and gabe rudy, vp of product & engineering. copy number variation (cnv) can be drivers in many genetic diseases and can be called using our clinical and research application platforms: varseq and svs, respectively. using these platforms, cnv are called using the existing coverage data stored in your bam files and are detected using a targeted or binned region approach. as the targeted approach has been demonstrated in previous webcasts, we wanted to focus on the binned region approach that is implemented for detecting cnv from shallow.. golden helix® is a global bioinformatics firm founded in 1998. we develop and sell an industry leading clinical solution that supports