1 code implementation • NeurIPS 2023 • Timothy F. Truong Jr, Tristan Bepler
Generative protein language models are a natural way to design new proteins with desired functions.
1 code implementation • 24 Oct 2022 • Alireza Nasiri, Tristan Bepler
Here, we consider the problem of learning semantic representations of objects that are invariant to pose and location in a fully unsupervised manner.
no code implementations • 5 Oct 2022 • Lin Li, Esther Gupta, John Spaeth, Leslie Shing, Tristan Bepler, Rajmonda Sulo Caceres
Therapeutic antibody development has become an increasingly popular approach for drug development.
no code implementations • 3 Apr 2022 • Soumya Ram, Tristan Bepler
We present the MSA-to-protein transformer, a generative model of protein sequences conditioned on protein families represented by multiple sequence alignments (MSAs).
1 code implementation • 1 Dec 2021 • Paul T. Kim, Alex J. Noble, Anchi Cheng, Tristan Bepler
Automating this is non-trivial: the images suffer from low signal-to-noise ratio and are affected by a range of experimental parameters that can differ for each collection session.
1 code implementation • NeurIPS 2019 • Tristan Bepler, Ellen D. Zhong, Kotaro Kelley, Edward Brignole, Bonnie Berger
Given an image dataset, we are often interested in finding data generative factors that encode semantic content independently from pose variables such as rotation and translation.
2 code implementations • ICLR 2020 • Ellen D. Zhong, Tristan Bepler, Joseph H. Davis, Bonnie Berger
Cryo-electron microscopy (cryo-EM) is a powerful technique for determining the structure of proteins and other macromolecular complexes at near-atomic resolution.
1 code implementation • ICLR 2019 • Tristan Bepler, Bonnie Berger
We introduce a framework that maps any protein sequence to a sequence of vector embeddings --- one per amino acid position --- that encode structural information.
1 code implementation • 22 Mar 2018 • Tristan Bepler, Andrew Morin, Julia Brasch, Lawrence Shapiro, Alex J. Noble, Bonnie Berger
Cryo-electron microscopy (cryoEM) is an increasingly popular method for protein structure determination.