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Fazle E. Faisal

Publications and source records attributed to Fazle E. Faisal.

2 recordsLinked to original sources

From homogeneous to heterogeneous network alignment via colored graphlets

Network alignment (NA) compares networks with the goal of finding a node mapping that uncovers highly similar (conserved) network regions. Existing NA methods are homogeneous, i.e., they can deal only with networks containing nodes and edges of one type. Due to increasing amounts of heterogeneous network data with nodes or edges of different types, we extend three recent state-of-the-art homogeneous NA methods, WAVE, MAGNA++, and SANA, to allow for heterogeneous NA for the first time. We introduce several algorithmic novelties. Namely, these existing methods compute homogeneous graphlet-based node similarities and then find high-scoring alignments with respect to these similarities, while simultaneously maximizing the amount of conserved edges. Instead, we extend homogeneous graphlets to their heterogeneous counterparts, which we then use to develop a new measure of heterogeneous node similarity. Also, we extend $S^3$, a state-of-the-art measure of edge conservation for homogeneous NA, to its heterogeneous counterpart. Then, we find high-scoring alignments with respect to our heterogeneous node similarity and edge conservation measures. In evaluations on synthetic and real-world biological networks, our proposed heterogeneous NA methods lead to higher-quality alignments and better robustness to noise in the data than their homogeneous counterparts. The software and data from this work is available upon request.

q-bio.MN↗

Network approach integrates 3D structural and sequence data to improve protein structural comparison

Initial protein structural comparisons were sequence-based. Since amino acids that are distant in the sequence can be close in the 3-dimensional (3D) structure, 3D contact approaches can complement sequence approaches. Traditional 3D contact approaches study 3D structures directly. Instead, 3D structures can be modeled as protein structure networks (PSNs). Then, network approaches can compare proteins by comparing their PSNs. Network approaches may improve upon traditional 3D contact approaches. We cannot use existing PSN approaches to test this, because: 1) They rely on naive measures of network topology. 2) They are not robust to PSN size. They cannot integrate 3) multiple PSN measures or 4) PSN data with sequence data, although this could help because the different data types capture complementary biological knowledge. We address these limitations by: 1) exploiting well-established graphlet measures via a new network approach, 2) introducing normalized graphlet measures to remove the bias of PSN size, 3) allowing for integrating multiple PSN measures, and 4) using ordered graphlets to combine the complementary PSN data and sequence data. We compare both synthetic networks and real-world PSNs more accurately and faster than existing network, 3D contact, or sequence approaches. Our approach finds PSN patterns that may be biochemically interesting.

q-bio.MN↗