Paper List
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Formation of Artificial Neural Assemblies by Biologically Plausible Inhibition Mechanisms
This work addresses the core limitation of the Assembly Calculus model—its fixed-size, biologically implausible k-WTA selection process—by introducing...
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How to make the most of your masked language model for protein engineering
This paper addresses the critical bottleneck of efficiently sampling high-quality, diverse protein sequences from Masked Language Models (MLMs) for pr...
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Module control in youth symptom networks across COVID-19
This paper addresses the core challenge of distinguishing whether a prolonged societal stressor (COVID-19) fundamentally reorganizes the architecture ...
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JEDI: Jointly Embedded Inference of Neural Dynamics
This paper addresses the core challenge of inferring context-dependent neural dynamics from noisy, high-dimensional recordings using a single unified ...
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ATP Level and Phosphorylation Free Energy Regulate Trigger-Wave Speed and Critical Nucleus Size in Cellular Biochemical Systems
This work addresses the core challenge of quantitatively predicting how the cellular energy state (ATP level and phosphorylation free energy) governs ...
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Packaging Jupyter notebooks as installable desktop apps using LabConstrictor
This paper addresses the core pain point of ensuring Jupyter notebook reproducibility and accessibility across different computing environments, parti...
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SNPgen: Phenotype-Supervised Genotype Representation and Synthetic Data Generation via Latent Diffusion
This paper addresses the core challenge of generating privacy-preserving synthetic genotype data that maintains both statistical fidelity and downstre...
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Continuous Diffusion Transformers for Designing Synthetic Regulatory Elements
This paper addresses the challenge of efficiently generating novel, cell-type-specific regulatory DNA sequences with high predicted activity while min...
Incorporating indel channels into average-case analysis of seed-chain-extend
Carnegie Mellon University, Pittsburgh, PA, USA
30秒速读
IN SHORT: This paper addresses the core pain point of bridging the theoretical gap for the widely used seed-chain-extend heuristic by providing the first rigorous average-case analysis that accounts for insertions and deletions (indels), not just substitutions.
核心创新
- Methodology Introduces a generalized definition of 'recoverability' and a 'homologous path' to mathematically model the correct alignment under indel mutation channels, moving beyond the simpler 'homologous diagonal' used for substitutions only.
- Theory Develops new mathematical machinery to handle the dependence structure of neighboring anchors and the existence of 'clipping anchors' (partially correct anchors), which are unique challenges introduced by indels.
- Theory Proves that under a total mutation rate θ_T < 0.159, optimal linear-gap cost chaining achieves an expected recoverability of ≥ 1 - O(1/√m), generalizing the prior substitution-only result to a biologically realistic model.
主要结论
- The expected recoverability of an optimal chain under linear-gap cost chaining is ≥ 1 - O(1/√m) when the total mutation rate θ_T (sum of substitution, insertion, deletion rates) is less than 0.159.
- The expected runtime of the algorithm is O(m n^(3.15·θ_T) log n). For example, at a θ_T of 0.05 (similar to human-chimp divergence), the exponent is ~1.12, leading to near-linear scaling.
- The analysis successfully bridges theory and practice by extending the proof framework to handle indels, justifying the heuristic's empirical effectiveness on real genomic data which contains indels.
摘要: Given a sequence s1 of n letters drawn i.i.d. from an alphabet of size σ and a mutated substring s2 of length m<n, we often want to recover the mutation history that generated s2 from s1. Modern sequence aligners are widely used for this task, and many employ the seed-chain-extend heuristic with k-mer seeds. Previously, Shaw and Yu showed that optimal linear-gap cost chaining can produce a chain with 1−O(1/m) recoverability, the proportion of the mutation history that is recovered, in O(mn^(2.43θ) log n) expected time, where θ<0.206 is the mutation rate under a substitution-only channel and s1 is assumed to be uniformly random. However, a gap remains between theory and practice, since real genomic data includes insertions and deletions (indels), and yet seed-chain-extend remains effective. In this paper, we generalize those prior results by introducing mathematical machinery to deal with the two new obstacles introduced by indel channels: the dependence of neighboring anchors and the presence of anchors that are only partially correct. We are thus able to prove that the expected recoverability of an optimal chain is ≥1−O(1/√m) and the expected runtime is O(mn^(3.15·θ_T) log n), when the total mutation rate given by the sum of the substitution, insertion, and deletion mutation rates (θ_T = θ_i + θ_d + θ_s) is less than 0.159.