Top Tweets for #GlobalGene
En el Día de la Tierra resaltamos la importancia de la #genómica y los esfuerzos en materia de secuenciación del #ADN, en la comprensión y conservación de la #biodiversidad de nuestro planeta 🧬🍀
#diadelatierra #diamundialdelatierra #EarthDay #GlobalGene #Genomics
❇️ Nuestro Manifiesto ❇️
#GlobalGene #GenómicaParaTodos #Genómica #GenomicsForAll #ADN #ciencia #Tecnología #Innovación #equidad #Diversidad #inclusion
Los invitamos a que nos den ideas y sugerencias sobre científicos o proyectos de genómica que quieran presentar en #GlobalGene 🧬🌎
@GonzagajMx @CientificasEC @OwsdColombia @mujerconciencia @genotipia @MPAlonso @gmrepetto @daniela_oaks @mlcepedah @gabydel
Hoy estamos lanzando @Global_Gene en Instagram.
Espacio para participar, aprender, compartir tus proyectos y dar voz a todos aquellos interesados en la genómica en el sur global 🧬🌎
https://t.co/uwZoKVnvcX
Lack of #diversity and poor representation of Latino and other populations in #genomics datasets should be addressed as a collective and #Global effort 🧬🌎
#GlobalGene #GenomicsForAll
#equity #inclusion #access
The Importance of Representation in Genetic Research
In the ever-evolving field of genomics, the data we collect and study has a profound impact on the future of healthcare. But there's an issue at the heart of this scientific advancement: not everyone is equally represented in genomic datasets. Why does this matter? Because without a comprehensive genetic blueprint of all human populations, we risk creating a healthcare system that only works for a few.
Imagine walking into a store knowing it only caters to 10% of the population — you'd feel left out, wouldn't you? That's what happens when genomic research overlooks vast swathes of the global population. Patients from underrepresented groups are less likely to benefit from the advancements in healthcare that genomics promises. This is the inequity we're currently facing, and it's one we must address to avoid perpetuating existing biases.
Our team has taken a deep dive into the representation of global data in genetic studies. We've looked at genome-wide association studies (GWAS), pharmacogenomics (how genes affect a person's response to drugs), clinical trials, and even the tests that consumers take at home to learn about their ancestry or health risks. The findings are a wake-up call: the genetic data we're currently collecting does not reflect global genetic diversity.
To put it simply, some populations are not being studied considering their numbers in the global census. This gap means we're missing out on the full picture of human genetic variation. And as we move towards an era where genomics informs everyday medical decisions, we can't afford to have blind spots if we are to fulfil the promise of precision medicine.
It's time for a strategic shift. We need to deliberately include diverse populations in genomic research. It's not just about adding numbers; it's about enriching our datasets with the variety of genetic data that humanity has to tell. This isn't a problem for future generations to solve — it's a challenge for us, here and now.
Ensuring that everyone is represented isn't just good science; it's a step towards a more equitable healthcare system where everyone benefits from the genomic revolution.
If you are interested to watch me live on this, then come to this event:
Equity, Diversity, and Inclusion for AI and Data Science 🌐
🗓 Date: Thursday, 29th February
🕖 Time: 19:00 - 20:00
📍 Location: C2.12 - Large Lecture, New Cavendish Campus, University of Westminster
https://t.co/JvSOKdcsiJ
https://t.co/bYI9vAnL5O
We wear what we care for. #globalgene #rarediseases #ordi #geneticconditions #ensowellness #physicalhealth #awareness #careandsupport #counsellor #aroubakabir #livewithcfdotcom https://t.co/D1iZdLCQIG

Hope appealing to highest authority will bring smiles to millions of #RareDiseases patients suffering in #India by implementing #RareDiseasepolicy #patientadvocacy #GlobalGene #MoHFW @JPNadda
ORDI is committed to #patientadvocacy Thanks to @ANI @EconomicTimes for coverage & support of our fight for #raredisease patients in India. Here are full PIL details: PIL W.P. (C) No. 39349 of 2018: ORDI Vs. Union of India & Ors. https://t.co/Cc5IqbxQb2
Article on #RettSyndrome #awareness And parent meeting #nimhans #Bengaluru. #ORDIndia #ExpressNews #GlobalGene @Harsharajasimha #RareDiseases #India

Panel discussion #NIMHANS 11th annual #Rettsyndrome #Awareness Meet @ #At #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation.
#ORDIndia #globalgene #rarediseases
#ORDI

Dr Rajani Khajuria #AIMS 11th annual #Rettsyndrome #Awareness Meet @ #At #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by
#ORDIndia #globalgene #rarediseases
#ORDI

Mr Samir Sethi President #IRSF says all are parents are great and special 11th annual #Rettsyndrome #Awareness Meet @ #At #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by Indian Rett syndrome Foundation.
#ORDIndia #globalgene #rarediseases

Thank you Dr K S Rana for your appreciation of my work at #ORDindia and #LSDSS in your inaugural address #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene #EveryLifeIsPrecious

Dr K S Rana address #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene .

Light lamping #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene #rarediseases #ORDIndia

Inaguration #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene #rarediseases #ORDIndia

Registration in process @ #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene #rarediseases

At #NIMHANS observing 11th annual #Rettsyndrome #Awareness Meet @ #bengaluru by #IRSF Indian Rett syndrome Foundation. #ORDI #globalgene #rarediseases

#GlobalGene https://t.co/iExXelFGQZ

New member #135 added to grp from PA today w/ #sclerosingmesenteritis #mesentericpanniculitis #rdla #raredisease #Orphandrug #globalgene
New member added from Ontario-133 people w/ #sclerosingmesenteritis and #mesentericpanniculitis #rdla #raredisease #Nord #NIH #globalgene
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