Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.

Wesley Wei Qian

dblp:263/2040 · DBLP profile ↗
← Back
5ranked-venue papers
1as first author
2since 2021 · last 2023
0000-0003-0726-575XORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 3 · 2 since 2021Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
4 papers
Bioinformatics and computational biology · 100%
Artificial intelligence
1 paper
Trustworthy machine learning · 75% Graph learning · 25%

Topics — the 13 heaviest of 14, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › molecular property prediction
binding affinity prediction
0.712023
3D Equivariant Diffusion for Target-Aware Molecule Generation and Affinity Prediction · ICLR 2023
Bioinformatics and computational biology
molecular property prediction
0.712023
3D Equivariant Diffusion for Target-Aware Molecule Generation and Affinity Prediction · ICLR 2023
Bioinformatics and computational biology › molecular informatics › cheminformatics
molecule generation
0.712023
3D Equivariant Diffusion for Target-Aware Molecule Generation and Affinity Prediction · ICLR 2023
Bioinformatics and computational biology › molecular informatics › cheminformatics › molecule generation
target-aware molecule generation
0.712023
3D Equivariant Diffusion for Target-Aware Molecule Generation and Affinity Prediction · ICLR 2023
Bioinformatics and computational biology › molecular informatics › molecular modeling
molecular conformation optimization
0.612022
Energy-Inspired Molecular Conformation Optimization · ICLR 2022
Machine learning › Trustworthy machine learning › interpretability › explanation evaluation
attribution evaluation
0.412020
Evaluating Attribution for Graph Neural Networks · NeurIPS 2020
Machine learning › Trustworthy machine learning › interpretability
attribution methods
0.412020
Evaluating Attribution for Graph Neural Networks · NeurIPS 2020
Machine learning › Graph learning
graph neural network
0.412020
Evaluating Attribution for Graph Neural Networks · NeurIPS 2020
Machine learning › Trustworthy machine learning
interpretability
0.412020
Evaluating Attribution for Graph Neural Networks · NeurIPS 2020
Bioinformatics and computational biology › omics data analysis
batch effect correction
0.412020
Batch equalization with a generative adversarial network · Bioinform. 2020
Bioinformatics and computational biology › bioimage informatics
bioimage analysis
0.412020
Batch equalization with a generative adversarial network · Bioinform. 2020
Bioinformatics and computational biology
protein engineering
0.412020
Evolutionary Context-Integrated Deep Sequence Modeling for Protein Engineering · RECOMB 2020
Bioinformatics and computational biology › protein sequence analysis
protein sequence modeling
0.412020
Evolutionary Context-Integrated Deep Sequence Modeling for Protein Engineering · RECOMB 2020

Methods — techniques the papers use, named apart from their topics

3d equivariant diffusion · 0.7energy-inspired optimization · 0.6style transfer · 0.4generative adversarial network · 0.4deep sequence modeling · 0.4benchmarking · 0.4StarGAN · 0.4
YearPublicationVenuePosition
2023 3D Equivariant Diffusion for Target-Aware Molecule Generation and Affinity Prediction
Jiaqi Guan, Wesley Wei Qian, Xingang Peng, Yufeng Su, Jian Peng 0001, Jianzhu Ma
ICLR2
2022 Energy-Inspired Molecular Conformation Optimization
Jiaqi Guan, Wesley Wei Qian, Qiang Liu 0001, Wei-Ying Ma, Jianzhu Ma, Jian Peng 0001
ICLR2
2020 Evaluating Attribution for Graph Neural Networks
abstract
Interpretability of machine learning models is critical to scientific understanding, AI safety, as well as debugging. Attribution is one approach to interpretability, which highlights input dimensions that are influential to a neural network’s prediction. Evaluation of these methods is largely qualitative for image and text models, because acquiring ground truth attributions requires expensive and unreliable human judgment. Attribution has been little studied for graph neural networks (GNNs), a model class of growing importance that makes predictions on arbitrarily-sized graphs. In this work we adapt commonly-used attribution methods for GNNs and quantitatively evaluate them using computable ground-truths that are objective and challenging to learn. We make concrete recommendations for which attribution methods to use, and provide the data and code for our benchmarking suite. Rigorous and open source benchmarking of attribution methods in graphs could enable new methods development and broader use of attribution in real-world ML tasks.
Benjamín Sánchez-Lengeling, Jennifer N. Wei, Brian K. Lee, Emily Reif, Wesley Wei Qian, Kevin McCloskey, Lucy J. Colwell, Alexander B. Wiltschko
NeurIPS6
2020 Evolutionary Context-Integrated Deep Sequence Modeling for Protein Engineering
Yunan Luo, Lam Vo, Hantian Ding, Yufeng Su, Yang Liu 0097, Wesley Wei Qian, Huimin Zhao 0007, Jian Peng 0001
RECOMB6
2020 Batch equalization with a generative adversarial network
abstract
MOTIVATION: Advances in automation and imaging have made it possible to capture a large image dataset that spans multiple experimental batches of data. However, accurate biological comparison across the batches is challenged by batch-to-batch variation (i.e. batch effect) due to uncontrollable experimental noise (e.g. varying stain intensity or cell density). Previous approaches to minimize the batch effect have commonly focused on normalizing the low-dimensional image measurements such as an embedding generated by a neural network. However, normalization of the embedding could suffer from over-correction and alter true biological features (e.g. cell size) due to our limited ability to interpret the effect of the normalization on the embedding space. Although techniques like flat-field correction can be applied to normalize the image values directly, they are limited transformations that handle only simple artifacts due to batch effect. RESULTS: We present a neural network-based batch equalization method that can transfer images from one batch to another while preserving the biological phenotype. The equalization method is trained as a generative adversarial network (GAN), using the StarGAN architecture that has shown considerable ability in style transfer. After incorporating new objectives that disentangle batch effect from biological features, we show that the equalized images have less batch information and preserve the biological information. We also demonstrate that the same model training parameters can generalize to two dramatically different types of cells, indicating this approach could be broadly applicable. AVAILABILITY AND IMPLEMENTATION: https://github.com/tensorflow/gan/tree/master/tensorflow_gan/examples/stargan. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Wesley Wei Qian, Cassandra Xia, Subhashini Venugopalan, Arunachalam Narayanaswamy, Michelle Dimon, George W. Ashdown, Jake Baum, Jian Peng 0001, D. Michael Ando
Bioinform.1