vaRHC: an R package for semi-automation of variant classification in hereditary cancer genes according to ACMG/AMP and gene-specific ClinGen guidelines. #VariantClassification#R#Bioinformatics
https://t.co/7EMA3gnsNY
At Frederick National Laboratory our employees share a common desire to help make a difference in cancer research and public health concerns. Apply today: https://t.co/Pz91H0dFk4 #Bioinformatics
Genomic data analysis can be complex, especially if you are new to NGS or do not have a computational background. Our latest guide https://t.co/3mqIiXiTKx provides a comprehensive overview of variant calling in genomics #AcademicResearch#Bioinformatics#Genomics#LifeSciences
Matt Geballe of @OpenEyeSoftware : For lead optimization, we are shipping Reaction & Reagent based enumeration tool for generating synthetically accessible molecules.
#openeyecup2023#orion#CADD#compchem
DDX41’s effects on innate immunity and tumor progression open the window to new therapeutic interventions. #drugdiscovery#biologyatwork https://t.co/wzn10JbIXK
An innovative Drug Discovery Program Management Ecosystem is coming! Remove technical obstacles slowing you down. Request your free consultation now. https://t.co/c6ePWtDMQE | #LifeSciences#Biotech#DrugDiscovery#BiotechNetworks
An innovative Drug Discovery Program Management Ecosystem is coming! Remove technical obstacles slowing you down. Request your free consultation now. https://t.co/H2JOsbwiai | #LifeSciences#Biotech#DrugDiscovery#BiotechNetworks
Coming up shortly: Listen to Soundside @KUOW@libdenk at 12:30 p.m. today 3/14 to hear Dr. Thomas Payne @UWDeptMedicine@UWMedicine#BioInformatics discuss ethical issues posed by growing market for people's health data. On 94.9 FM or Smart Speaker: Play KUOW.