Alan Rubin
@rubin_af
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Trying to figure out what genomic variants do. Computational biologist at @WEHI_research. Previously @uwgenome. Mastodon: https://t.co/6EtfEJxhLP
Melbourne, Australia
Joined June 2015
Very excited to share our new platform for distributing and analyzing MAVE datasets. Visit the database at and check out the visualizations at or directly from a MaveDB page.
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RT @dgmacarthur: Wonderful presentation from Eric Green (@NHGRI_Director) at @MCRI_for_kids discussing the history of genomics and the futu….
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RT @deciphergenomic: Jeremy Arbesfeld presenting pivotal work @ccg2024 about a framework for mapping MAVE data, which has allowed DECIPHER….
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Really proud of this work, the result of a fantastic international collaboration among experts brought together by @varianteffects. Huge thanks to everyone involved!.
Check out our paper: Minimum information and guidelines for reporting a multiplexed assay of variant effect. Great team effort through the AVE alliance @varianteffects @MelinaClaussnit @vnparikh Alex Wagner @Bennibolo @rubin_af
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RT @LindorffLarsen: Guidelines for releasing a variant effect predictor. By @BenLivesey6 @jmarshlab and other members of the atlas of @vari….
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RT @MoezDawood: Excited to announce our preprint using MAVEs to reduce variant classification disparities in underrepresented populations a….
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RT @dgmacarthur: We’ve just been awarded AU$10M from the Medical Research Future Fund to support the development of OurDNA, a new program t….
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RT @QIMRBerghofer: Congratulations to @rubin_af, Amanda Spurdle, Hamish Scott, @BelindaPhipson, Paul James, @dougfowler42, .@lea_starita, C….
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I'm delighted to be leading this project with such a great team. Looking forward to bringing MAVE technology into the clinic here in Australia! Shout out to all my fellow @varianteffects members who are contributing to this mission locally and internationally.
I am excited to be able to announce that our MRFF grant to use Multiplex Assays of Variant Effect (MAVEs) to improve clinical interpretation of variants was successful!.
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RT @BelindaPhipson: I'm looking for a research officer/post doc to join my newly established group at WEHI. 2 year position, Level A6 - A8….
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RT @uwmnewsroom: Debbie Nickerson's @uwgenome contributions to human genome science & medical genetics, passionate support of women & train….
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RT @CEGS_CMAP: 📣 New publication from our group 📰"Closing the gap: Systematic integration of multiplexed functional data resolves variants….
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RT @JennyBryan: @CMastication I'm afraid this glorious bit has not ever been recorded 😂. But I can give you a better link to use:. https://t….
speakerdeck.com
Low-tech common sense about filenames. Prepared under the auspices of the Reproducible Science Curriculum (https://github.com/Reproducible-Science-Curri…
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RT @shalinhnaik: Very proud (and nervous) to announce my first podcast!! We are getting scientists, doctors and comedians to talk about CO….
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RT @CEGS_CMAP: Excited for our sister NHGRI Center at UW, which will focus on scaling up and applying technologies developed by our CMAP in….
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RT @lea_starita: @dougfowler42 and I are excited to announce the Center for Actionable Variant Analysis 🍾 has been funded by the NHGRI and….
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RT @TheNobleDust: Here's my review in @hmg_journal on the latest and greatest multiplex assays for linking human variants to disease phenot….
academic.oup.com
Abstract. The application of genomics to medicine has accelerated the discovery of mutations underlying disease and has enhanced our knowledge of the molec
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