Golden Helix, Inc.

Quality control is key when it comes to genomic data, and our latest blog dives into how VarSeq's automated pipeline makes QC both efficient and seamless. With built-in tools for flagging inconsistencies, monitoring variant quality, and automating complex workflows, VarSeq is empowering labs to streamline their NGS analysis. Whether you're processing high-throughput data or managing a clinical workflow, VarSeq ensures top-notch accuracy and reliability every step of the way. Read the full blog here: https://bit.ly/4e7uKIn #GoldenHelix #VarSeq #NGS #Genomics #PrecisionMedicine #Bioinformatics #DataAutomation #QualityControl #GeneticAnalysis

VarSeq is powering groundbreaking genetic research, and we couldn’t be more excited to showcase how customers are using it to make key discoveries! From advancing cancer genomics to solving complex cases in rare diseases, VarSeq is the go-to solution for simplifying variant analysis and accelerating research. With robust tools for annotation, filtering, and interpretation, VarSeq is empowering labs to push the boundaries of genomic science. Read the full blog here: https://bit.ly/3Avszk5 #GoldenHelix #VarSeq #Genomics #GeneticResearch #NGS #PrecisionMedicine

We're heading to #ASHG24, and we can't wait to share some exciting innovations! Whether you're curious about the latest in NGS workflows, automation, or cancer capabilities, we've got something for you. Come visit us at booth #959 in Denver, CO, from November 6-8 to see firsthand how Golden Helix is advancing precision medicine with our powerful software solutions. Don't miss out on our exclusive demos and talks—mark your calendar and swing by to say hello! Check out the full details: https://bit.ly/3C8Yis4 #GoldenHelix #ASHG24 #NGS #PrecisionMedicine #CancerResearch #VarSeq #PGx #GeneticAnalysis

Did you miss our webcast yesterday? No worries, we have the recording available! Yesterday, our Director of Field Application Services, J. Darby Kammeraad, presented our latest VSPGx updates and VarSeq 2.6.2. This webcast introduced our CypCaller tool, designed for accurate CYP2D6 calling for short-read whole genome sequencing. Also, VSPGx importer updates for importing star alleles and more comprehensive PGx reporting updates. If you are interested to learn more I encourage you to visit our website and watch the recording! #PGx #Pharmacogenomics #ShortRead #WholeGenome #Genetics #NGS

The latest gnomAD 4.1 release is here, bringing enhanced allele frequency data straight to your VarSeq workflows! Our latest blog dives into the latest release and how these improvements can elevate your genomic workflows with VarSeq. #Genomics #VarSeq #gnomAD #ClinicalGenomics #GoldenHelix #NGS

 Join us for a webcast on the advancements in pharmacogenomics reporting with VarSeq 2.6.2! Discover how the latest features can enhance your genomic analysis and improve patient care. Our team will dive deep into the innovative tools designed to streamline reporting and interpretation, empowering you to make more informed decisions. Don’t miss this opportunity to elevate your understanding of pharmacogenomics and see how VarSeq can transform your workflow! #Pharmacogenomics #Genomics #VarSeq #Webcast #GoldenHelix

Read our latest blog on how VarSeq is revolutionizing somatic interpretation with flexible biomarker reporting capabilities. With our tools, researchers and clinicians can easily navigate complex genomic data and customize reports to meet their specific needs. This means more accurate insights and improved patient care! Dive into the blog to learn how VarSeq is making somatic interpretation easier than ever. Learn more here: https://bit.ly/48hhO1u #Genomics #Biomarkers #Somatic #GoldenHelix

Big news! VarSeq 2.6.2 is here and packed with powerful new features! Whether you’re streamlining your NGS analysis or diving into complex genetic datasets, our latest update enhances the user experience with improved workflows, annotation updates, and so much more! Ready to see how VarSeq 2.6.2 can elevate your research? Check out all the details in our latest blog post: https://bit.ly/3ZXE0LH #Genomics #NGS #Bioinformatics #PrecisionMedicine #GoldenHelix

Dive into the world of compound heterozygosity and its significance in genetic analysis. Our latest blog covers how VarSeq 2.6.2 simplifies the detection of compound heterozygosity between SNPs and CNVs, helping to improve diagnostic accuracy for recessive disorders. Don't miss this detailed breakdown! Read more: https://bit.ly/4dxjmFw #NGS #Genetics #CompoundHeterozygosity #VarSeq #Bioinformatics

Explore the power of VarSeq! Our latest blog dives into how VarSeq is transforming research in inherited diseases and cancer. Learn how customers use its advanced tools to uncover genetic insights and accelerate their work. Get the details here: https://bit.ly/4gFwAmj