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arXiv research

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168,657 papers · 148 categories

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78155233310 · Jun 202019922001200920172026
48 results for DNA design

We propose generative neural network methods to generate DNA sequences and tune them to have desired properties. We present three approaches: creating synthetic DNA sequences using a generative adversarial network; a DNA-based variant of the activation maximization ("deep dream") design method; and a joint procedure wh…

2017-12-17abs ↗pdf ↗

A faster method for optimizing DNA and protein sequences using machine learning.

problem Designing DNA and protein sequences with improved function.
method Activation maximization with a straight-through approximation and adaptive entropy variable.
result Fast SeqProp achieves up to 100-fold faster convergence and improved fitness optima.

Many researches demonstrated that the DNA methylation, which occurs in the context of a CpG, has strong correlation with diseases, including cancer. There is a strong interest in analyzing the DNA methylation data to find how to distinguish different subtypes of the tumor. However, the conventional statistical methods …

2018-08-02abs ↗pdf ↗

Paper uses transfer learning and Bayesian optimization to reduce DNA sequence design experiments.

problem Designing many similar DNA sequences for specific applications is expensive and time-consuming.
method Combines transfer learning with Bayesian optimization to reduce experiment count.
result Total number of experiments can be significantly reduced by sharing information between tasks.

An evolutionary algorithm separates mixed DNA profiles in forensic genetics.

problem Deconvolving mixed DNA profiles from crime samples.
method Multiple population evolutionary algorithm (MEA) with guided mutation.
result The MEA successfully deconvoluted DNA profiles from crime samples.

A novel framework refines diffusion models iteratively for better downstream reward optimization.

problem Optimizing reward functions during inference of diffusion models.
method Iterative refinement process with noising and reward-guided denoising steps.
result Superior empirical performance in protein and DNA design.

Algorithm optimizes biological sequences using bootstrapped training with a score-conditioned generator.

problem Optimizing biological sequences for a black-box score function.
method Bootstrapped training of score-conditioned generator (BootGen) algorithm.
result Our method outperforms competitive baselines on biological sequential design tasks.

This research adapts superpixels for Shapley value computation in DNA profile classification.

problem Efficiently computing Shapley values for large, multidimensional time-series data.
method Adapting the concept of superpixels to streamline Shapley value computation for time-series-like data.
result Realistic, accurate, and fast computation of Shapley values for DNA profile classification.

The protein recombinase can change the knot type of circular DNA. The action of a recombinase converting one knot into another knot is normally mathematically modeled by band surgery. Band surgeries on a 2-bridge knot N((4mn-1)/(2m)) yielding a (2,2k)-torus link are characterized. We apply this and other rational tangl…

2011-08-03abs ↗pdf ↗

DNAS disentangles neural architecture search for better interpretability and performance.

problem Lack of interpretability in existing neural architecture search methods.
method DNAS disentangles the hidden representation of the controller into semantically meaningful concepts.
result DNAS achieves state-of-the-art performance and competitive architectures.

New method optimizes diffusion models without fine-tuning, integrating soft value functions.

problem Optimizing natural design spaces of images, molecules, DNA, RNA, and protein sequences.
method Iterative sampling method integrating soft value functions into diffusion model inference.
result Directly utilizes non-differentiable features/reward feedback, applies to discrete diffusion models.

This paper is an introduction to rational tangles, rational knots and links and their applications to DNA. The paper can be read as an introduction to our more technical papers on rational tangles (math.GT/0311499) and on rational knots (math.GT/0212011). The present paper includes a self-contained account of the tangl…

2003-11-27abs ↗pdf ↗

We study two systems of tangle equations that arise when modeling the action of the Integrase family of proteins on DNA. These two systems--direct and inverted repeats--correspond to two different possibilities for the initial DNA sequence. We present one new class of solutions to the tangle equations. In the case of i…

2004-12-23abs ↗pdf ↗

A deep probabilistic model analyzes DNA-encoded library data for efficient screening.

problem Complex data from DNA-encoded library experiments mask underlying signals.
method Compositional deep probabilistic model of DEL data, modeling latent reactions between synthons.
result DEL-Compose model demonstrates strong performance and valuable insights.

In this paper we propose network methodology to infer prognostic cancer biomarkers based on the epigenetic pattern DNA methylation. Epigenetic processes such as DNA methylation reflect environmental risk factors, and are increasingly recognised for their fundamental role in diseases such as cancer. DNA methylation is a…

2015-06-17abs ↗pdf ↗

When analyzing the genome, researchers have discovered that proteins bind to DNA based on certain patterns of the DNA sequence known as "motifs". However, it is difficult to manually construct motifs due to their complexity. Recently, externally learned memory models have proven to be effective methods for reasoning ov…

2017-02-22abs ↗pdf ↗

We consider the task of detecting regulatory elements in the human genome directly from raw DNA. Past work has focused on small snippets of DNA, making it difficult to model long-distance dependencies that arise from DNA's 3-dimensional conformation. In order to study long-distance dependencies, we develop and release …

2017-10-03abs ↗pdf ↗

We present a probabilistic modeling framework and adaptive sampling algorithm wherein unsupervised generative models are combined with black box predictive models to tackle the problem of input design. In input design, one is given one or more stochastic "oracle" predictive functions, each of which maps from the input …

2018-10-08abs ↗pdf ↗

We consider learning parameters of Binomial Hidden Markov Models, which may be used to model DNA methylation data. The standard algorithm for the problem is EM, which is computationally expensive for sequences of the scale of the mammalian genome. Recently developed spectral algorithms can learn parameters of latent va…

2018-02-07abs ↗pdf ↗

With different genomes available, unsupervised learning algorithms are essential in learning genome-wide biological insights. Especially, the functional characterization of different genomes is essential for us to understand lives. In this book chapter, we review the state-of-the-art unsupervised learning algorithms fo…

2015-08-03abs ↗pdf ↗

Study on the structure of classifier boundaries in DNA sequencing.

problem Understanding the structure of boundaries in a Bayes classifier for DNA sequencing.
method Examined the structure of the boundary in a Bayes classifier applied to DNA sequencing data. Introduced a new measure of uncertainty, Neighbor Similarity.
result The boundary is large and complex, and Neighbor Similarity effectively measures classifier uncertainty.

Study of Betti numbers in prodsimplicial complexes for directed graphs, focusing on DNA recombination.

problem Analyzing Betti numbers in directed graphs for DNA recombination.
method Custom prodsimplicial complexes for acyclic directed graphs, investigating Betti numbers.
result Investigated Betti numbers and cycles in prodsimplicial complexes for DNA recombination.

We categorise coherent band (aka nullification) pathways between knots and 2-component links. Additionally, we characterise the minimal coherent band pathways (with intermediates) between any two knots or 2-component links with small crossing number. We demonstrate these band surgeries for knots and links with small cr…

2014-08-08abs ↗pdf ↗

We develop an algorithm for minimizing a function using nn batched function value measurements at each of TT rounds by using classifiers to identify a function's sublevel set. We show that sufficiently accurate classifiers can achieve linear convergence rates, and show that the convergence rate is tied to the difficu…

2018-04-11abs ↗pdf ↗

We propose a dynamic neighborhood aggregation (DNA) procedure guided by (multi-head) attention for representation learning on graphs. In contrast to current graph neural networks which follow a simple neighborhood aggregation scheme, our DNA procedure allows for a selective and node-adaptive aggregation of neighboring …

2019-04-09abs ↗pdf ↗

Graph Canonical Correlation Analysis improves CCA for multiomics datasets.

problem Limited ability of conventional CCA methods to incorporate structured patterns in cross-correlation matrices.
method Graph Canonical Correlation Analysis (gCCA) calculates canonical correlations based on the graph structure of cross-correlation matrices.
result gCCA outperforms competing CCA methods in simulations and multiomics dataset analysis.

Chirality affects the curvature of molecular networks, influencing their shape and stability.

problem Understanding how chirality influences the curvature of molecular networks.
method Langevin dynamics simulations and constrained gradient optimization of square lattice networks.
result Linking chirality dictates the sign of Gaussian curvature in molecular chainmail networks.

In this paper, we study a geometric/topological measure of knots and links called the nullification number. The nullification of knots/links is believed to be biologically relevant. For example, in DNA topology, one can intuitively regard it as a way to measure how easily a knotted circular DNA can unknot itself throug…

2011-01-06abs ↗pdf ↗

The research reported in this paper identifies the epigenetic biomarker (methylation beta pattern) of breast cancer. Many cancers are triggered by abnormal gene expression levels caused by aberrant methylation of CpG sites in the DNA. In order to develop early diagnostics of cancer-causing methylations and to develop a…

2019-10-12abs ↗pdf ↗

The paper studies pseudo links in genus g handlebodies, generalizing knot theory.

problem Modeling DNA knots with missing crossing information.
method Introducing pseudo links as mixed pseudo links in S^3, generalizing Kauffman bracket polynomial and Alexander theorem.
result The theory of pseudo links is closely related to singular links and can be applied to study singular links in genus g handlebodies.

GIDS reduces high-dimensional response and predictor spaces, improving interpretability and computational efficiency.

problem Challenges in modeling interactions among high-dimensional multimodal data.
method Graph Independence Dual Screening (GIDS) framework that reduces both response and predictor dimensions.
result GIDS reduces feature space to 9,000 CpGs and 2,000 transcripts, revealing coordinated regulatory mechanisms.

Novel U-learning method for predicting continuous outcomes from high-dimensional data.

problem Challenges in making valid inferences on predictions from high-dimensional inputs.
method U-learning via combinatory multi-subsampling for ensemble predictions and confidence intervals.
result Valid inferences on predictions from Lasso and neural networks.