Euformatics @Euformatics
Euformatics provides software and expert computational services for NGS where life sciences and software development meet. euformatics.com Espoo, Finland Joined August 2013-
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On Tuesday we had the pleasure of meeting Christophe Roos, co-founder of @Euformatics, a company developing NGS analytics. Thanks Christophe for joining our career lunch!
Hienoa, että @Euformatics menestyy! Tästä hyötyvät myös potilaat. @HealthtechFi hs.fi/visio/art-2000…
Euformatics Signs Distribution Deal With Saudi Arabia's Al-Jeel genomeweb.com/business-news/…
Exciting news! We are pleased to announce our new distribution partnership with Aljeel Medical for the Kingdom. #ngs #saudiarabia #finland #genetics #illumina #medicalgenetics #dna #aljeel #biology euformatics.com/blog/euformati…
Euformatics Eyes Global Expansion in NGS Informatics genomeweb.com/informatics/eu…
Euformatics Partners With Síntese Biotecnologia to Enter Latin American Market genomeweb.com/business-news/…
Do you perform Next Generation sequencing? Want to check the quality of your NGS data? Then enrol in our 2021 EQA! For full details see genqa.org/news #NGS @UKNEQAS #quality #data @Euformatics @EMQNOffice
we are hiring #developers #espoo #clinical #genetics #software euformatics.com/careers/
Excellent animation of use of genomics data for healthcare. It is impossible to achieve without interoperable standards for data access, regulation and technology. BUT Once all works, positive impact on healthcare e.g. diagnostics is crystal clear. @ELIXIREurope @B1MG_Project
Excellent animation of use of genomics data for healthcare. It is impossible to achieve without interoperable standards for data access, regulation and technology. BUT Once all works, positive impact on healthcare e.g. diagnostics is crystal clear. @ELIXIREurope @B1MG_Project
Do you use Polyphen-2, SIFT, REVEL, GAVIN or ClinPred for interpreting clinical variants? Should you? Are more tools better than one? Some answers in our work using a unique clinically relevant dataset out this week! jmg.bmj.com/content/early/…
The Individual Laboratory Report (ILR) and EQA Summary report for the joint GenQA/EMQN NGS germline/somatic EQAs has been released. Log in to your GenQA account to get your results! #NGS @EMQNOffice #EQA #proficiencytesting @Euformatics
Introducing the NextSeq™ 2000, our most advanced benchtop sequencer. Explore groundbreaking ideas with higher efficiency, fewer restraints, and more emerging applications. Learn more: ilmnmkt.illumina.com/2016004043 #ExperienceNextSeq2000 #JPM20 #JPMHC20
Christophe Roos korosti DigIT Popup -lavalla laadun merkityksestä genomitiedon hyödyntämisessä yksittäisen potilaan eduksi. @Euformatics @HealthtechFi #Lääkäri2020
Euformatics, UK Quality Assessment Organizations Expand Partnership to Include CNV Data genomeweb.com/sequencing/euf…
We are hiring! #Bioinformatics #softwaredevelopment #SoftwareJobs euformatics.com/careers/
Ouch. * Cancer only exome pipelines are unreliable - 69% of somatic mutations are false positives * 34-80% somatic variants appearing to contribute to intratumor genetic heterogeneity are technical noise
Ouch. * Cancer only exome pipelines are unreliable - 69% of somatic mutations are false positives * 34-80% somatic variants appearing to contribute to intratumor genetic heterogeneity are technical noise
More good news this week! Euformatics is happy to be a part of the quest to prevent autism. linkedin.com/feed/update/ac… #ASD #autismspectrumdisorders #genomics #H2020 #autism #sequencing @EU_H2020
Great idea from @traingene and @dnasko to look at all past RefSeq versions and show how Kraken classifications depend heavily on the database. Our new paper: genomebiology.biomedcentral.com/articles/10.11…
Say you pick 100 random bioinformatics software tools -- how many will you actually be able to access, install, and run? Our new paper: biorxiv.org/content/early/…
Say you pick 100 random bioinformatics software tools -- how many will you actually be able to access, install, and run? Our new paper: biorxiv.org/content/early/…
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