GenoQuanta’s Post

While genome sequencing is not being routinely used in medicine, we expect that things will be quite different by the end of the decade, as ongoing studies demonstrate how best to use genomic information in clinical care. Advances in DNA-sequencing technologies since the end of the Human Genome Project have led to more powerful ways to study the genomic bases of human disease. As researchers continue to study both rare and common genetic diseases, important details about the genomic architecture of a wide range of human disorders will emerge. I encourage you to learn more about DNA sequencing using our recently updated Talking Glossary of Genomic & Genetic Terms! https://lnkd.in/gue6RUZ7  

Unleashing the Power of Genomic Evolution with Next-Generation Sequencing (NGS) Insights Let's discuss the four crucial elements within this arena.✅ ▪️NGS Revolutionizes Genetic Analysis: Unmatched accuracy redefines genetic analysis, surpassing conventional methods. ▪️Revamped Personalized Medicine: Healthcare undergoes a transformation with tailored treatments derived from individual genetics. ▪️NGS Speeds Diagnostic Precision: Swift, targeted disease detection and treatment redefine diagnostic approaches. ▪️Expansive Influence Beyond Healthcare: NGS innovations extend their reach across diverse fields, promising widespread impact. Join Forces for Precision Medicine، Share your insights to collectively shape the future of NGS-driven precision medicine!✅ #PrecisionMedicine #GenomicSequencing #NGSDrivenPrecision #RapidDiagnosis

Genomic medicine has the potential to transform people’s lives by enabling faster diagnosis, matching patients to the most effective treatments, and monitoring treatment response. Our data resources, research and training are essential for making genomic medicine a reality. Find out how we work with Genomics England and NHS England to support the implementation of genomics in clinical settings. https://lnkd.in/eGtc74vY #genomicmedicine #precisionmedicine #genomics #genome #bioinformatics #DNA #healthcare #training #cancer #raredisease #dataanalysis #lifesciences #opendata #openscience #research #medicine #nhs

Based on an article in NPJ Genomic Medicine, which was co-authored by Dr. Pengfei Liu, Associate Clinical Director of NGS and Molecular at Baylor Genetics, clinical Whole Genome Sequencing (WGS) is becoming a routine, first-tier test for patients with rare genetic disorders as the standard of care in the evaluation of children and adults with a suspected genetic condition. At Baylor Genetics, test results for Rapid WGS are available in just five days. For more details and to start a test order, visit: https://bit.ly/42iERVj Read the article here: https://bit.ly/42KvHRS #ThinkBG #BGreat #RapidWGS #GenomeSequencing #NICU #PICU

Explore the world of mitochondrial genome analysis with our NGS Panel. It's a versatile tool for personalized healthcare, from diagnosing diseases to tracking progress. Get ready to delve into the fascinating realm of genetic medicine! 🌐🔍 Learn more here >> https://lnkd.in/gDVAkk5p #PMCDX #Pharmacogenomics #MitochondrialGenome

While the use of genomic information in medicine is not yet routine, we believe that the situation will be quite different by the end of the decade as ongoing research informs how best to implement genomic medicine! So far, improvements in DNA sequencing technologies since the end of the Human Genome Project have led to advances in the study of human diseases. As researchers continue to study both rare and common genetic diseases,  new details about the genomic architecture of a wide range of human disorders are emerging. I encourage you to learn more about DNA sequencing using our newly updated Talking Glossary of Genomic & Genetic Terms! https://lnkd.in/gue6RUZ7 

A decade ago, research demonstrating the promise of CRISPR sparked a wealth of interest in genome editing. We learned that while it held so much potential, we needed to find a way to ensure precision and safety to be a viable option for patients. That is exactly what we are doing at EmendoBio and we are dedicated to realizing the full potential that genomic medicine offers. #GenomicMedicine #EmendoBio #CRISPR

It's now officially accepted in Nature Genomic Medicine! I introduce a new paradigm for investigating sickle cell disease that could bring new biological and therapeutic targets for patients with sickle cell disease. # Sickle for Space # Novel gene-environmental targets

A group of researchers did their part to #EndAlz by characterizing the epigenomic, genomic, transcriptomic, and cellular underpinnings of #Alzheimers disease at the #singlecell level. See how they did it in our new blog, and spread the word for #AlzheimersAwareness month!

🔬 Bridging the Gap: Genome Analysis in Clinical Workflows 🏥 Genome analysis is reshaping clinical workflows, offering personalized insights for better patient care. At GenomAnalysis, we integrate the finest genomic techniques into clinical settings, empowering healthcare professionals with actionable genetic information. From diagnosing rare diseases to guiding treatment decisions, our advanced genomic solutions streamline clinical workflows and improve patient outcomes. Join us in revolutionizing healthcare through the power of genomics. #GenomAnalysis #ClinicalGenomics #HealthcareInnovation