Iterative progressive alignment method (IPAM) for multiple sequence alignment

Author(s):  
Farhana Naznin ◽  
Ruhul Sarker ◽  
Daryl Essam
2014 ◽  
Vol 23 (3) ◽  
pp. 261-275 ◽  
Author(s):  
Widad Kartous ◽  
Abdesslem Layeb ◽  
Salim Chikhi

AbstractMultiple sequence alignment (MSA) is one of the major problems that can be encountered in the bioinformatics field. MSA consists in aligning a set of biological sequences to extract the similarities between them. Unfortunately, this problem has been shown to be NP-hard. In this article, a new algorithm was proposed to deal with this problem; it is based on a quantum-inspired cuckoo search algorithm. The other feature of the proposed approach is the use of a randomized progressive alignment method based on a hybrid global/local pairwise algorithm to construct the initial population. The results obtained by this hybridization are very encouraging and show the feasibility and effectiveness of the proposed solution.


Author(s):  
Agung Widyo Utomo

Progressive multiple sequence alignment ClustalW is a widely used heuristic method for computing multiple sequence alignment (MSA). It has three stages: distance matrix computation using pairwise alignment, guide tree reconstruction using neighbor-joining and progressive alignment. To accelerate computing for large data, the progressive MSA algorithm needs to be parallelized. This research aims to identify, decompose and implement the pairwise alignment and neighbor-joining in progressive MSA using message passing, shared memory and hybrid programming model in the computer cluster. The experimental results obtained shared memory programming model as the best scenario implementation with speed up up to 12 times.


2005 ◽  
Vol 03 (02) ◽  
pp. 243-255 ◽  
Author(s):  
YI WANG ◽  
KUO-BIN LI

We describe an exhaustive and greedy algorithm for improving the accuracy of multiple sequence alignment. A simple progressive alignment approach is employed to provide initial alignments. The initial alignment is then iteratively optimized against an objective function. For any working alignment, the optimization involves three operations: insertions, deletions and shuffles of gaps. The optimization is exhaustive since the algorithm applies the above operations to all eligible positions of an alignment. It is also greedy since only the operation that gives the best improving objective score will be accepted. The algorithms have been implemented in the EGMA (Exhaustive and Greedy Multiple Alignment) package using Java programming language, and have been evaluated using the BAliBASE benchmark alignment database. Although EGMA is not guaranteed to produce globally optimized alignment, the tests indicate that EGMA is able to build alignments with high quality consistently, compared with other commonly used iterative and non-iterative alignment programs. It is also useful for refining multiple alignments obtained by other methods.


2010 ◽  
Vol 439-440 ◽  
pp. 35-40
Author(s):  
Zhan Mao Cao ◽  
Wen Jun Xiao ◽  
Li Min Peng

A brand new performance assessment model is proposed for multiple sequence alignment. The new strategy is based on beam constructing of DC-BTA algorithm, which is a Divide-and-Conquer alignment method with beams. Beams form blocks of almost the identical columns and contribute biggest similarity weight to sequences. A formula to compute all beam areas covering a sequence assigns a value or weight to the sequence. And the total beam area is a partial to the whole alignment. A rate value between 0 and 1 is computed to assess the performance. This scheme is a simple and effective assessment policy in DC-BTA for the convenience of collecting the beam areas.


2000 ◽  
Vol 47 (4) ◽  
pp. 1019-1026 ◽  
Author(s):  
E A Czuryło

Seven highly conserved regions were found in caldesmon molecules from various sources using the multiple sequence alignment method. Their localization coincides with regions where the binding sites to other proteins were postulated. Less conserved and highly divergent regions of the sequences are described as well. These results could refine the planning of caldesmon gene manipulations and accelerate the precise localization of binding sites in the caldesmon molecule and, as a consequence, this could help to elucidate its function in smooth muscle contraction.


2008 ◽  
Vol 06 (03) ◽  
pp. 521-541 ◽  
Author(s):  
ZEFENG ZHANG ◽  
HAO LIN ◽  
MING LI

Multiple sequence alignment is a classical and challenging task. The problem is NP-hard. The full dynamic programming takes too much time. The progressive alignment heuristics adopted by most state-of-the-art works suffer from the "once a gap, always a gap" phenomenon. Is there a radically new way to do multiple sequence alignment? In this paper, we introduce a novel and orthogonal multiple sequence alignment method, using both multiple optimized spaced seeds and new algorithms to handle these seeds efficiently. Our new algorithm processes information of all sequences as a whole and tries to build the alignment vertically, avoiding problems caused by the popular progressive approaches. Because the optimized spaced seeds have proved significantly more sensitive than the consecutive k-mers, the new approach promises to be more accurate and reliable. To validate our new approach, we have implemented MANGO: Multiple Alignment with N Gapped Oligos. Experiments were carried out on large 16S RNA benchmarks, showing that MANGO compares favorably, in both accuracy and speed, against state-of-the-art multiple sequence alignment methods, including ClustalW 1.83, MUSCLE 3.6, MAFFT 5.861, ProbConsRNA 1.11, Dialign 2.2.1, DIALIGN-T 0.2.1, T-Coffee 4.85, POA 2.0, and Kalign 2.0. We have further demonstrated the scalability of MANGO on very large datasets of repeat elements. MANGO can be downloaded at and is free for academic usage.


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