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I figure I should also make an introduction. I'm an RA in the Roth Lab at UofT and I work on Multiplexed Assays of Variant Effects and their use toward clinical variant interpretation.

Optimization of a deep mutational scanning workflow to improve quantification of mutation effects on protein-protein interactions biorxiv.org/content/10.1101/20

BioRxiv has joined forces with Company of Biologists to expand our presence on Mastodon.

Mastodon accounts now available for every subject category connect.biorxiv.org/news/2023/

“In a large study published in September 2022 ..researchers developed a tool that’s essentially a library of every conceivable change to the N-protein over time. They used deep mutational scanning to predict how each of those changes would affect the ability of 17 antibodies used in 11 commercially available rapid tests to latch onto the virus… can cross-reference changes in each new variant of the virus to quickly assess whether a given test will still work. “

cell.com/cell/fulltext/S0092-8

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Our new #git #cheatsheet is ready for use, thanks to @SciCompAalto: aaltoscicomp.github.io/cheatsh

It's designed for beginners/intermediates to introduce things slowly, recognizing that most use is simple, and grouping advanced uses together how they are used. It'll be used in our workshop next week. #RSEng #HPC #teaching

For all the folks starting their #PhD (or their master thesis) today - a reminder why your PhD advisor can solve a problem so "easily" ...

#astrodon #academia #AcademiChatter #research

Code sharing increases citations but remains uncommon

doi.org/10.21203/rs.3.rs-32222

'We examine temporal trends in code sharing in ecology and evolution publications since 2010.

We find that scientists are overwhelmingly (95%) failing to publish their code.

We also find code sharing can considerably improve citations.'

#openscience #code #ecopubs

My favorite paper that I've read this year — a look at how confusion between inferential uncertainty and outcome variability creates all sorts of problems — is now out in PNAS.

Here's the paper: pnas.org/doi/abs/10.1073/pnas.

Here's the thread I wrote about the preprint last April: fediscience.org/@ct_bergstrom/

Optimizing #RShiny applications with webR is a game-changer 🤯 By leveraging browser-based computation, we witness a significant reduction in server load and enhanced responsiveness.

Dive deeper into the technical insights: appsilon.com/bringing-webr-int

#webR #RStats

alright #rstats , no cheating -- without running it beforehand, what would you expect this code to do?

add <- function(a, b) {
a + b
} / 2

add(2, 4)

Just discovered there is an extension of #Inkscape to quickly edit scientific figures (change axis ratio, font sizes, etc) 🤩

github.com/burghoff/Scientific

The approach itself is implemented in multidms software package, which is available at github.com/matsengrp/multidms

We think it should also be useful to other labs performing deep mutational scanning across protein variants or selection conditions.

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In new study, we develop rigorous method to jointly analyze deep mutational scanning of different protein homologs or conditions

We use it to identify mutations w effects on spike-mediated viral entry that differ by >1,000-fold among #SARSCoV2 strains.

biorxiv.org/content/10.1101/20

Is it left handed or this some sort of optical illusion? 🧐
---
RT @hajirasouliha
A DNA double helix molecule made of drones! #AGBT23
twitter.com/hajirasouliha/stat

Announcing papertooter. Papertooter is a simple script that takes the URL of a biorxiv preprint, and posts the title and link to the paper on Mastodon using the Mastodon Python API. It also posts a unique hashtag it generates from the paper's DOI.

Feature requests and bug reports welcome.

github.com/idoerg/papertooter

Postdoctoral position in deep mutational scanning

Join our group at #LU to apply #deep-mutational-scanning to study how efficient folding of proteins is encoded in the cell.

bit.ly/3WIN0jp
#ScienceJobs
Lund, #Sweden #PostdoctoralFellow
bit.ly/3WIN0jp

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