We're sending you and your families warm wishes this holiday season from everyone at SOPHiA GENETICS!
#HappyHolidays #SeasonsGreetings #Winter #EndOfYear
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SOPHiA GENETICS is a health tech company democratizing Data-Driven Medicine to improve medical research worldwide - youtube.com/watch?v=8RAsKm
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Whether you are an experienced user or brand new to Alamut™ Visual Plus, this new technical note will help you navigate variant analysis with ease.
Get it now: ter.li/fxkc2k
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
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Our Swiss colleagues are ringing in the holiday season and making spirits bright! We invited families and their children to celebrate with festive activities and they even had a visit with Santa. 🎄🎅🎄
#HappyHolidays #SeasonsGreetings #Holidays #Celebration
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Accelerate your pediatric research with optimized sample-to-report workflows. Discover SOPHiA DDM™ Solutions for Pediatric Diseases: ter.li/esi65d
#pediatrics #rarediseases #inheriteddiseases
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Whether you are an experienced user or brand new to Alamut™ Visual Plus, our new technical note will help you navigate variant analysis with ease.
Get it now: ter.li/fxkc2k
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
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Accurately characterize the complex mutational landscape of hereditary cancers with the SOPHiA DDM™️ Comprehensive Hereditary Cancer Solution.
Download: ter.li/l3li9g
#sophiaddm #herditarycancer #sequencing #VariantInterpretation #DataDrivenMedicine
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Take a look at what our CEO recently told readers about finding inspiration every day:
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We're saying beignYAY at #ASH22! Stop by booth #1915 to grab a sweet treat and chat with our sales team.
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Right now at #ASH22: SOPHiA GENETICS BioPharma solutions provide real-world data insight on the KITGene in Systemic Mastocytosis
DETAILS: ter.li/tbutox
#ClinicalResearch #biopharma
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Put children’s #kidneyhealth first.
Rapidly identify alterations in 40+ genes associated with dysfunction and failure, and leverage SOPHiA DDM™ Nephropathies Solution to streamline your #pediatric research – from sample to interpretation.
Learn more: ter.li/esi65d
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The SOPHiA DDM™ for Blood Cancers portfolio allows detection and characterization of complex genomic variants, while adhering to most up-to-date international guidelines. Meet our experts at #ASH22 to learn if it could be right for you! ter.li/d7lz2p
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You asked. We listened. We are thrilled to introduce a new feature on Alamut™ Visual Plus. Along with SNVs and Indels, you can now annotate and visualize structural variants, including CNVs. Learn more: ter.li/bb2j9l
#alamutvisualplus #genomics #bioinformatics #NGS
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Learn how the SOPHiA DDM™ HRD Solution supports accurate HRD detection for research. WATCH & CLICK HERE for more: ter.li/bb2w8g
#CancerResearch #OvarianCancer #PrecisionMedicine #DataDrivenMedicine #CancerMoonshot #HRD #SOPHiADDM #DeepLearning #DataDrivenMedicine
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Comprehensive variant annotation, enhanced variant visualization, and efficient laboratory workflows can streamline your variant assessment.
Start a free trial of Alamut™ Visual Plus to see it for yourself: ter.li/mg4fkf
#Genomics #NGS #variantanalysis
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On December 2 and 3, our Swiss Offices joined #Telethon to raise awareness of #rarediseases.
Our colleagues have dazzled us with their baking skills, and we're pleased to have raised CHF 375, matched by SOPHiA GENETICS, to fund social initiatives & research through Telethon.
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Did you miss it? Watch the replay of our panel discussion at BioTechX and discover how multimodal health data and AI/ML could work together to democratize precision medicine and transform clinical practices. Watch it now: ter.li/zyx720
#BioTechX #multimodaldata #Webinar
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Two innovative technologies in one webinar!
Watch our ESMO 2022 talks on HRD and RNAtarget solutions that took place on September 10 in Paris, now available on demand.
Part 1 on SOPHiA DDM™ Dx HRD Solution: ter.li/tw1v97
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Accurately characterize the complex mutational landscape of hereditary cancers with the SOPHiA DDM™️ Comprehensive Hereditary Cancer Solution.
Download: ter.li/l3li9g
#sophiaddm #herditarycancer #sequencing #VariantInterpretation #DataDrivenMedicine
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This week we were present at 2022 where we had the pleasure to participate in ’s One-stop Clinic Experience for Breast. We had the opportunity to talk about integrating radiology and genomics to power the future of precision medicine.
#RSNA #GEHealthcare
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Hematological tumors are the 4th most frequent cancer in the developed world. This #ASH22 to learn how the seamless SOPHiA DDM™ for Blood Cancers portfolio offers researchers competitive advantages that can positively impact disease study.
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With over 1 million genomic profiles sequenced, SOPHiA DDM™ is fed a wealth of diverse data that can help you find unique insights.
Learn more on our blog ter.li/c1ynea
#GenomicAnalysis #GenomicData #MachineLearning #SOPHiADDM
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Discover how Alamut™ Visual Plus implements nomenclature guidelines to enhance accurate variant analysis.
Download your technical note now: ter.li/fxkc2k
#variantanalysis #genomics #NGS #variantannotation #bioinformatics
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Hear about two Canadian hospitals in Ontario and how they designed their future-proof hereditary cancer panel in line with Provincial Hereditary Cancer Testing requirements.
Download: ter.li/l3li9g
#sophiaddm #herditarycancer #sequencing #VariantInterpretation
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Congrats to our own Abhi Verma for being listed among the top 25 Healthcare Technology CTOs of 2022 - ter.li/4yedfg
#CTO #PrecisionMedicine #DataDrivenMedicine
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Accelerate the complex and time-consuming assessment of variants with Alamut™ Visual Plus.
Request a free trial to experience the user-friendly interface and integrated variant annotation and analysis features: ter.li/mg4fkf
#Genomics #NGS #variantanalysis
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Want to learn more about the #DeepLearning capabilities of SOPHiA DDM™ Homologous Recombination Deficiency (HRD) Solution?
We sat down with the solution’s lead developer, Christian Pozzorini, to discuss the technology behind our HRD algorithm. READ:
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Two innovative technologies in one webinar!
Watch our ESMO 2022 talks on HRD and RNAtarget solutions that took place on September 10 in Paris, now available on demand.
Part 1 on SOPHiA DDM™ Dx HRD Solution: ter.li/tw1v97
Did you miss it? Discover how genetic experts saved time, reduced costs, and improved the yield of their hereditary cancer and rare disease NGS testing in this recap of our ASHG symposium: ter.li/dwgdb5
#genomics #NGS #bioinformatics #ASHG2022
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On this #WorldChildrensDay, we reaffirm our commitment to streamlining #pediatric research.
With simplified sample-to-report workflows, SOPHiA DDM™ helps you pinpoint variants with potential impact on child development.
Find out more: ter.li/esi65d
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We’ll be in the Big Easy this December for #ASH22! Meet our experts and learn how SOPHiA DDM™ for Blood Cancers can help you! #hematology #SOPHiADDM
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SOPHiA DDM™ has sequenced over 1 million genomic profiles, see how our experts say this is making our platform more accurate by giving it access to a diverse data set in our new blog ter.li/c1ynea
#GenomicAnalysis #GenomicData #MachineLearning #SOPHiADDM
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Healthcare software company Sophia Genetics has partnered with Microsoft to accelerate health data analysis, improve healthcare workflows and create new opportunities in precision medicine. buff.ly/3Uur760
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Are you thinking about having your own future-proof custom sequencing panel for hereditary cancers?
Read the case study to find out how two hospitals in Ontario managed to get the best out of the SOPHiA DDM™️ Set-up program.
Download case study: ter.li/l3li9g
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SOPHiA GENETICS™ Integrated Solutions makes #germline #NGS testing easier even without an in-house lab by pairing you with one of our partner labs.
Simply send your samples and receive analyzed NGS data for interpretation.
Learn more: ter.li/wm7qdx
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Did you know that today is National Future Day in Switzerland? Children are invited to come to work with mom and dad and test out some potential career choices. Thanks to all of our participants for visiting our labs in Rolle!
#NationalFutureDay #KidsAtWork #DataDrivenMedicine
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Two innovative technologies in one webinar!
Watch our ESMO 2022 talks on HRD and RNAtarget solutions that took place on September 10th in Paris, now available on demand.
Part 1 on SOPHiA DDM™ Dx HRD Solution: ter.li/tw1v97
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This is our last day at BioData World Congress, come and meet us at our booth #99 and learn more about our approach to multimodal data.
#BioTechX #multimodaldata #PrecisionMedecine #DataDrivenMedicine
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Have a listen to what our Chief BioPharma Officer Peter Casasanto told RSK Life Science Media before our presentation at #BiotechX "Hope or Hype?: The importance of Multimodal Data Integration to Advance Precision Medicine". WATCH VIDEO: ter.li/dkwdbf
#PrecisionMedicine
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Our fantastic panel on Importance of #multimodal data integration in advancing #precisionmedicine
#BioTechX
Memorial Sloan-Kettering Cancer Center
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