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An Improved (and Practical) Parameterized Algorithm for the Individual Haplotyping Problem MFR with Mate-Pairs

机译:带有配对的个体单体型问题MFR的一种改进的(实用)参数化算法

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The Individual Haplotyping MFR problem is a computational problem that, given a set of DNA sequence fragment data of an individual, induces the corresponding haplotypes by dropping the minimum number of fragments. Bafna, Istrail, Lancia, and Rizzi proposed an algorithm of time O(22k m 2 n+23k m 3) for the problem, where m is the number of fragments, n is the number of SNP sites, and k is the maximum number of holes in a fragment. When there are mate-pairs in the input data, the parameter k can be as large as 100, which would make the Bafna-Istrail-Lancia-Rizzi algorithm impracticable. The current paper introduces a new algorithm PM-MFR of running time O(nk23k2+mlogm+mk1)O(nk_{2}3^{k_{2}}+mlog m+mk_{1}) , where k 1 is the maximum number of SNP sites that a fragment covers (k 1 is smaller than n), and k 2 is the maximum number of fragments that cover a SNP site (k 2 is usually about 10). Since the time complexity of the algorithm PM-MFR is not directly related to the parameter k, the algorithm solves the Individual Haplotyping MFR problem with mate-pairs more efficiently and is more practical in real biological applications.
机译:个体单体型MFR问题是一个计算问题,在给定个体DNA序列片段数据集的情况下,它会通过丢弃最小数量的片段来诱导相应的单体型。 Bafna,Istrail,Lancia和Rizzi提出了时间O(2 2k m 2 n + 2 3k m 3 < / sup>),其中m是片段数,n是SNP位点数,k是片段中的最大空洞数。当输入数据中有配对时,参数k可以最大为100,这将使Bafna-Istrail-Lancia-Rizzi算法不可行。本文介绍了一种新的运行时间为O(nk 2 3 k 2 + mlogm + mk 1 < / sub>)O(nk_ {2} 3 ^ {k_ {2}} + mlog m + mk_ {1}),其中k 1 是片段覆盖的最大SNP位点数( k 1 小于n),k 2 是覆盖SNP位点的最大片段数(k 2 通常约为10 )。由于算法PM-MFR的时间复杂度与参数k没有直接关系,因此该算法可以更有效地解决伴侣配对的单倍型MFR问题,并且在实际生物学应用中更加实用。

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