Paper List
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Macroscopic Dominance from Microscopic Extremes: Symmetry Breaking in Spatial Competition
This paper addresses the fundamental question of how microscopic stochastic advantages in spatial exploration translate into macroscopic resource domi...
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Linear Readout of Neural Manifolds with Continuous Variables
This paper addresses the core challenge of quantifying how the geometric structure of high-dimensional neural population activity (neural manifolds) d...
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Theory of Cell Body Lensing and Phototaxis Sign Reversal in “Eyeless” Mutants of Chlamydomonas
This paper solves the core puzzle of how eyeless mutants of Chlamydomonas exhibit reversed phototaxis by quantitatively modeling the competition betwe...
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Cross-Species Transfer Learning for Electrophysiology-to-Transcriptomics Mapping in Cortical GABAergic Interneurons
This paper addresses the challenge of predicting transcriptomic identity from electrophysiological recordings in human cortical interneurons, where li...
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Uncovering statistical structure in large-scale neural activity with Restricted Boltzmann Machines
This paper addresses the core challenge of modeling large-scale neural population activity (1500-2000 neurons) with interpretable higher-order interac...
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Realizing Common Random Numbers: Event-Keyed Hashing for Causally Valid Stochastic Models
This paper addresses the critical problem that standard stateful PRNG implementations in agent-based models violate causal validity by making random d...
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A Standardized Framework for Evaluating Gene Expression Generative Models
This paper addresses the critical lack of standardized evaluation protocols for single-cell gene expression generative models, where inconsistent metr...
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Single Molecule Localization Microscopy Challenge: A Biologically Inspired Benchmark for Long-Sequence Modeling
This paper addresses the core challenge of evaluating state-space models on biologically realistic, sparse, and stochastic temporal processes, which a...
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.