Javier Mendoza-Revilla

576 posts

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Javier Mendoza-Revilla

Javier Mendoza-Revilla

@JavierMenRev

Computational Geneticist @instadeepai and adjunct lecturer at @CayetanoHeredia. Previously at @UGI_at_UCL🇬🇧 and @institutpasteur🇫🇷. Views my own.

Paris, France Se unió Şubat 2013
575 Siguiendo760 Seguidores
Javier Mendoza-Revilla retuiteado
Bernardo Almeida
Bernardo Almeida@deAlmeida_BP·
🚀 Introducing Nucleotide Transformer v3 (NTv3) Today, we are very excited to share our latest foundation model for biology - Nucleotide Transformer v3 (NTv3). NTv3 is @instadeepai new multi-species genomics foundation model, designed for 1 Mb, single-nucleotide-resolution prediction, and for bridging representation learning, sequence-to-function modeling, and generative regulatory design within a single framework 🧬 This work was developed in close collaboration with @AlexanderStark8 , @volokuleshov , and @pkoo562 , and reflects several years of joint effort at the intersection of machine learning and regulatory genomics.
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Nature Methods
Nature Methods@naturemethods·
Nucleotide Transformer is a series of genomics foundation models of different parameter sizes and training datasets which can be applied to various downstream tasks by fine-tuning. @instadeepai nature.com/articles/s4159…
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Yun S. Song
Yun S. Song@yun_s_song·
We were invited to write a review article on DNA/genomic language models (gLMs). We took this occasion to gather our thoughts on promising applications, and major considerations for developing and evaluating gLMs. Pls share with your colleagues: Preprint: arxiv.org/abs/2407.11435
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Thomas Pierrot
Thomas Pierrot@thomas_pierrot·
Very proud to announce ChatNT, the first multimodal conversational agent for biological sequences🧬. ChatNT can be simply prompted with a question and a nucleotide sequence to solve DNA, RNA and Protein tasks 🧑‍🔬! 📚Paper: tinyurl.com/chatNT-pdf 🌐Blog: tinyurl.com/chatNT-blog
InstaDeep@instadeepai

The NT Family is growing! 🐣 ✨ Introducing ChatNT, a Conversational Agent designed to analyse genomics sequences and address a wide range of key biological questions, assisting scientists in their daily work 👩‍🔬 📚Paper: tinyurl.com/chatNT-pdf 🌐Blog: tinyurl.com/chatNT-blog

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Javier Mendoza-Revilla retuiteado
Jian Zhou
Jian Zhou@zhou_jian·
Glad that our sequence model of promoters in human genome is now published in @ScienceMagazine. Check out the paper for a deep dive into the sequence basis of transcription initiation at the basepair level: science.org/doi/10.1126/sc…
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InstaDeep
InstaDeep@instadeepai·
✨ Meet SegmentNT: the first-ever LLM capable of annotating DNA sequences at single nucleotide resolution. Built on top of our Nucleotide Transformer, SegmentNT offers precise genome annotation surpassing traditional methods and can offer deeper insights into our genome 🧬
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InstaDeep
InstaDeep@instadeepai·
InstaDeep's @JavierMenRev will share how AI systems - and LLMs specifically - deepen our understanding of the Maize genome tomorrow at 7:20 pm at the Maize Genetics Meeting in Raleigh, NC. #MGM2024 Read the paper: biorxiv.org/content/10.110…
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Bernardo Almeida
Bernardo Almeida@deAlmeida_BP·
I am looking for PhD research interns at the @instadeepai Paris office for the coming summer. Join us if you are interested in DNA LLMs and regulatory genomics! We have different projects available and are flexible to find one that fits your PhD. Link: instadeep.com/internship-off…
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StarkLab
StarkLab@stark_lab·
We are very excited to present a major breakthrough achievement – the de novo design of synthetic enhancers for selected tissues in fruit fly embryos in vivo using deep- and transfer learning, @deAlmeida_BPet al published today in @Nature nature.com/articles/s4158…. Thread 👇(1/N)
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Lluis Quintana-Murci
Lluis Quintana-Murci@QuintanaMurci·
If you are interested in gene-environment interactions, molecular phenotypes and single-cell genomics, join us at ⁦@institutpasteur⁩ in the sunny Paris! Post-doctoral position in single-cell genomics at Institut Pasteur in Paris docs.google.com/document/d/e/2…
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Javier Mendoza-Revilla
Javier Mendoza-Revilla@JavierMenRev·
@AxelOlin2 Yes, the adoption of this type of screening would need to be extremely widespread for it to have a significant effect on the population level. But, yes, that was essentially my point on pleiotropy—we wouldn't know how we are affecting other phenotypes.
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Javier Mendoza-Revilla@JavierMenRev·
(2) GWAS Transferability: PRS show much greater accuracy in individuals of European ancestry than in others. Thus, the PRS they report may be highly inaccurate for many individuals (admixed/from underrepresented populations) and potentially even irrelevant for some.
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Javier Mendoza-Revilla
Javier Mendoza-Revilla@JavierMenRev·
(1) Pleiotropy: Meaning, a variant at a locus can affect multiple traits simultaneously. Also, pleiotropy can be antagonistic, implying that a variant may be simultaneously harmful AND beneficial. What, then, will these types of screenings be selecting for?
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