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Maggie Arriaga

@maggie-arriaga.bsky.social
47 followers 63 following 8 posts

Genetics PhD Candidate & NSF GRFP Fellow @StanfordMed BA @Kenyon College Interested in all things splicing and rare disease!

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Reposted by Maggie Arriaga
GREGoR Consortium @gregor-research.bsky.social · 19/09/2025
Thank you to all our members and collaborators for an inspiring and productive @gregor-research.bsky.social meeting last week in San Diego! ☀️🧬 #RareDisease #Research
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Maggie Arriaga @maggie-arriaga.bsky.social · 07/01/2025
What if one variant can cause splicing outliers transcriptome-wide? In our preprint, we show how examining transcriptome-wide patterns of splicing outliers can both diagnose individuals with rare spliceopathies and uncover novel disease-gene relationships! (www.medrxiv.org/content/10.1...)
medrxiv.org
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies
RNA-sequencing has improved the diagnostic yield of individuals with rare diseases. Current analyses predominantly focus on identifying outliers in single genes that can be attributed to cis-acting va...
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Reposted by Maggie Arriaga
GREGoR Consortium @gregor-research.bsky.social · 12/12/2024
We've created a Starter Pack with GREGoR Cosortium Members: go.bsky.app/KW4m3zR Let us know if you're a part of GREGoR and would like to be added!
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Reposted by Maggie Arriaga
Rachel Ungar @raungar.bsky.social · 13/11/2024
Congratulations to my mentee Maggie Maurer, an ASHG Trainee Research Excellence Pre-Doctoral Winner. She discovered a new disease gene in her rotation project last year! The critical method for this project was shared with us by collaborator Vijay Ganesh and clinical work was done by Rodrigo Mendez.
two scientists standing in front of ASHG banner smiling
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Reposted by Maggie Arriaga
Moez Dawood @moezdawood.bsky.social · 20/12/2024
🚨 Excited to announce the Marker paper for the GREGoR Consortium! arxiv.org/abs/2412.14338 Accelerating #RareDisease diagnostics with cutting-edge #Genomics and global data sharing of omics and deep phenotyping from ~7500 individuals on NHGRI AnVIL and much more to come! 🧬
arxiv.org
GREGoR: Accelerating Genomics for Rare Diseases
Rare diseases are collectively common, affecting approximately one in twenty individuals worldwide. In recent years, rapid progress has been made in rare disease diagnostics due to advances in DNA seq...
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