Paper List
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The Effective Reproduction Number in the Kermack-McKendrick model with age of infection and reinfection
This paper addresses the challenge of accurately estimating the time-varying effective reproduction number ℛ(t) in epidemics by incorporating two crit...
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Covering Relations in the Poset of Combinatorial Neural Codes
This work addresses the core challenge of navigating the complex poset structure of neural codes to systematically test the conjecture linking convex ...
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Collective adsorption of pheromones at the water-air interface
This paper addresses the core challenge of understanding how amphiphilic pheromones, previously assumed to be transported in the gas phase, can be sta...
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pHapCompass: Probabilistic Assembly and Uncertainty Quantification of Polyploid Haplotype Phase
This paper addresses the core challenge of accurately assembling polyploid haplotypes from sequencing data, where read assignment ambiguity and an exp...
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Setting up for failure: automatic discovery of the neural mechanisms of cognitive errors
This paper addresses the core challenge of automating the discovery of biologically plausible recurrent neural network (RNN) dynamics that can replica...
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Influence of Object Affordance on Action Language Understanding: Evidence from Dynamic Causal Modeling Analysis
This study addresses the core challenge of moving beyond correlational evidence to establish the *causal direction* and *temporal dynamics* of how obj...
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Revealing stimulus-dependent dynamics through statistical complexity
This paper addresses the core challenge of detecting stimulus-specific patterns in neural population dynamics that remain hidden to traditional variab...
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Exactly Solvable Population Model with Square-Root Growth Noise and Cell-Size Regulation
This paper addresses the fundamental gap in understanding how microscopic growth fluctuations, specifically those with size-dependent (square-root) no...
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.