Efficient Computation of Sequence Mappability

Sequence mappability is an important task in genome resequencing. In the ( k ,  m )-mappability problem, for a given sequence T of length n , the goal is to compute a table whose i th entry is the number of indices j ≠ i such that the length- m substrings of T starting at positions i and j have at m...

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Published inAlgorithmica Vol. 84; no. 5; pp. 1418 - 1440
Main Authors Charalampopoulos, Panagiotis, Iliopoulos, Costas S., Kociumaka, Tomasz, Pissis, Solon P., Radoszewski, Jakub, Straszyński, Juliusz
Format Journal Article
LanguageEnglish
Published New York Springer US 01.05.2022
Springer Nature B.V
Springer Verlag
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ISSN0178-4617
1432-0541
1432-0541
DOI10.1007/s00453-022-00934-y

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Summary:Sequence mappability is an important task in genome resequencing. In the ( k ,  m )-mappability problem, for a given sequence T of length n , the goal is to compute a table whose i th entry is the number of indices j ≠ i such that the length- m substrings of T starting at positions i and j have at most k mismatches. Previous works on this problem focused on heuristics computing a rough approximation of the result or on the case of k = 1 . We present several efficient algorithms for the general case of the problem. Our main result is an algorithm that, for k = O ( 1 ) , works in O ( n ) space and, with high probability, in O ( n · min { m k , log k n } ) time. Our algorithm requires a careful adaptation of the k -errata trees of Cole et al. [STOC 2004] to avoid multiple counting of pairs of substrings. Our technique can also be applied to solve the all-pairs Hamming distance problem introduced by Crochemore et al. [WABI 2017]. We further develop O ( n 2 ) -time algorithms to compute all ( k ,  m )-mappability tables for a fixed m and all k ∈ { 0 , … , m } or a fixed k and all m ∈ { k , … , n } . Finally, we show that, for k , m = Θ ( log n ) , the ( k ,  m )-mappability problem cannot be solved in strongly subquadratic time unless the Strong Exponential Time Hypothesis fails. This is an improved and extended version of a paper presented at SPIRE 2018.
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ISSN:0178-4617
1432-0541
1432-0541
DOI:10.1007/s00453-022-00934-y