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Rosen, Y.

Publications and source records attributed to Rosen, Y..

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An average-case sublinear exact Li and Stephens forward algorithm

Hidden Markov models of haplotype inheritance such as the Li and Stephens model allow for computationally tractable probability calculations using the forward algorithms as long as the representative reference panel used in the model is sufficiently small. Specifically, the monoploid Li and Stephens model and its variants are linear in reference panel size unless heuristic approximations are used. However, sequencing projects numbering in the thousands to hundreds of thousands of individuals are underway, and others numbering in the millions are anticipated.\n\nTo make the Li and Stephens forward algorithm for these datasets computationally tractable, we have created a numerically exact version of the algorithm with observed average case [O](nk0.35) runtime, avoiding any tradeoff between runtime and model complexity. We demonstrate that our approach also provides a succinct data structure for general purpose haplotype data storage. We discuss generalizations of our algorithmic techniques to other hidden Markov models.\n\n2012 ACM Subject ClassificationTheory of computation {longrightarrow} Streaming, sublinear and near linear time algorithms; Applied computing {longrightarrow} Bioinformatics\n\nSupplement Materialhttps://github.com/yoheirosen/sublinear-Li-Stephens.\n\nFundingThis work was supported by the National Human Genome Research Institute of the National Institutes of Health under Award Number 5U54HG007990, the National Heart, Lung, and Blood Institute of the National Institutes of Health under Award Number 1U01HL137183-01, and grants from the W.M. Keck foundation and the Simons Foundation.\n\nAcknowledgementsWe would like to thank Jordan Eizenga for his helpful discussions throughout the development of this work.

bioinformatics

Describing the Local Structure of Sequence Graphs

Analysis of genetic variation using graph structures is an emerging paradigm of genomics. However, defining genetic sites on sequence graphs remains an open problem. Patens invention of the ultra-bubble and snarl, special subgraphs of sequence graphs which can identified with efficient algorithms, represents important first step to segregating graphs into genetic sites. We extend the theory of ultrabubbles to a special subclass where every detail of the ultrabubble can be described in a series and parallel arrangement of genetic sites. We furthermore introduce the concept of bundle structures, which allows us to recognize the graph motifs created by additional combinations of variation in the graph, including but not limited to runs of abutting single nucleotide variants. We demonstrate linear-time identification of bundles in a bidirected graph. These two advances build on initial work on ultrabubbles in bidirected graphs, and define a more granular concept of genetic site.

bioinformatics

Modelling haplotypes with respect to reference cohort variation graphs

Current statistical models of haplotypes are limited to panels of haplotypes whose genetic variation can be represented by arrays of values at linearly ordered bi- or multiallelic loci. These methods cannot model structural variants or variants that nest or overlap. A variation graph is a mathematical structure that can encode arbitrarily complex genetic variation. We present the first haplotype model that operates on a variation graph-embedded population reference cohort. We describe an algorithm to calculate the likelihood that a haplotype arose from this cohort through recombinations and demonstrate time complexity linear in haplotype length and sublinear in population size. We furthermore demonstrate a method of rapidly calculating likelihoods for related haplotypes. We describe mathematical extensions to allow modelling of mutations. This work is an essential step forward for clinical genomics and genetic epidemiology since it is the first haplotype model which can represent all sorts of variation in the population.

genomics