Top Tweets for #MastermindGSE
Thank you #ESHG2023 and everyone who visited our booth to connect with our team! Get in touch to schedule your #MastermindGSE demo if we missed you at the event: https://t.co/9PthWVdSKA

📣 The #MastermindGSE team is excited to announce that we have made several enhancements to our supplemental file matching to help you save time & augment your genomic evidence search experience. Read the latest blog & watch the quick tutorial: https://t.co/NPblOAtMFy

👉Our latest blog is a recap of our #MastermindGSE User Group in Salt Lake City where we met with valued customers & learned from expert speakers from @Intermountain @myriadgenetics & @agavig Connectics Consulting. TY to all who attended!
https://t.co/ZcRyemdArO

We're proud to work with the @RadyGenomics team & making #genomics actionable for patients with #rarediseases🧬
Read more via @FortuneMagazine https://t.co/2UrgwH360l
#projectbabybear #MastermindGSE #WGS
Reduce turn around time, increase diagnostic yield and accelerate throughput with #MastermindGSE 🖥️🧬 Meet our specialists at #ACMGmtg23 Booth 1107 to demo the most up-to-date & comprehensive source of genomic evidence!
#genomics #variantinterpretation #ACMG @TheACMG

Our first #MastermindGSE User Group has been a great success! Thank you to our valued users and guest speakers @agavig of Connetics Consulting, @Intermountain & @myriadgenetics for sharing your insights & expertise🧬

👋🤝 Meet the team at #ACMGMtg23! Visit our event page to schedule your #MastermindGSE demo 💻🧬Add @DrMarkKiel's Exhibit Theater talk to your calendar 🗓️👉 https://t.co/KOxUSev2eg
#genomics #ACMG2023 #NBS

🧬 We’ve added copy number variants (CNVs) to the Mastermind API for programmatic use! This shows all CNVs in a given article associated with a disease or gene. See the new #MastermindGSE feature https://t.co/m6cZvg9bcl
#genomics #bioinformatics #genechat

Attending @APHL 2022 #APHLNBS?
Stop by the @CDCgov booth & say Hi 👋 to Genomenon's Matts Bell and Brittney Jones. Ask our experts about how #MastermindGSE is the engine behind the future of Newborn Sequencing.
Learn more about this event: https://t.co/9p1mGqjcZd

Our latest blog outlines case study examples with @LurieChildrens where #MastermindGSE's AI-driven search capacity is proven as a critical resource to multiple clinical cases. Read more:
https://t.co/oufIiac4M1
#genomics #blog #bioinformatics #CNVs
Register for our next webinar to learn how to streamline variant interpretation workflow within a single easily searchable interface using #MastermindGSE & the new ClinVar integration. Sign up today! https://t.co/VPDdc58eFA
#genomics #bioinformatics #webinar #genechat

#PRESSRELEASE We are pleased to announce that Genomenon has integrated all the variants and pathogenicity interpretations from the #ClinVar database into #MastermindGSE. Read more about the latest update: https://t.co/MrmQeIWrkw
#genomics #bioinformatics #genechat

Speaking today @CG_Consortium #CGCannual2022 at 10:30am CT is Genomenon's Clinical Product Manager, Dan O'Hara. Be sure to stop by our booth to ask us about #MastermindGSE!

Reduce turnaround time, increase diagnostic yield and accelerate throughput with #MastermindGSE 🧬🖥️
Get started with a complimentary trial of Professional Edition & talk to us about multiple licenses for your lab➡️https://t.co/y4LXQUcqvb
#genomics #genechat #clinicalresearch

Registration is now open for our next webinar with expert speakers from @LurieChildrens & Genomenon | JULY 21 - 11amEDT | Learn more & sign up ➡️ https://t.co/cYTRBstzNs
#genomics #webinar #CNVs #genechat #bioinformatics #MastermindGSE

There's still time to register for today's webinar: #ACMG Classification for #RareDisease. Join expert speakers at 11am EDT for the live discussion! https://t.co/yw26yrpUvL
#genomics #webinar #genechat #MastermindGSE

We're pleased to announce our partnership with @Agilent to integrate #MastermindGSE into the new version of Agilent Alissa Interpret 🧬🖥️ Read the official press release announcement: https://t.co/3yjeGkSWNC

In our latest #blog CTO @jangosteve describes the limitations of the Mastermind Cited Variants Reference (CVR) that affect genomic analyses & how the integration of #MastermindGSE’s API can help surmount them. Read more: https://t.co/4n9OSUCRFv

TOMORROW! Register now for the #MastermindGSE Masterclass webinar at 11am EST 🧬🖥️ Learn about Search Companion for @googlechrome & how to accelerate your variant interpretation efforts! https://t.co/3sJG2M2rTt
#genomics #bioinformatics #webinar

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