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Ali, W.

Publications and source records attributed to Ali, W..

8 recordsLinked to original sources

A Scalable Distributed-Memory MPI Implementation of Smith-Waterman with Token-Passing Traceback

As genomic sequencing produces increasingly massive datasets, accurate local sequence alignment via the Smith-Waterman(SW) algorithm remains computationally prohibitive due to its space and quadratic time complexity O(mn). While parallelization addresses a path forward, existing MPI-based solutions present a critical bottleneck during the traceback phase, either omitting it entirely or gathering the entire direction matrix to a single root node, which severely limits scalability. To overcome this, we propose a fully distributed Message Passing Interface (MPI) implementation featuring a token passing traceback scheme. Our approach distributes the directional matrix across all participating ranks, reducing per-rank memory footprint from O(mn) to O(mn/p), thereby enabling the alignment of sequences far beyond the capacity of sequential or centralized parallel methods. We validate our method on real human DNA sequences (BRCA1, BRCA2, Titin, chr1, chr2) and synthetic datasets up to 50kx50k. Results demonstrate that this MPI implementation aligns 98kx98k real DNA (chr1xchr2) in 58.9160 seconds across 16 MPI processes, a task where the sequential baseline fails due to out-of-memory errors. We achieve best speedups on synthetic data of 19.30x (40kx40k, 16 MPI processes) and on real DNA data is 13.39x (BRCA1xTitin, 8 MPI processes), while capping per-rank memory for the largest dataset at just 573 MB. By enabling exact, memory-scalable alignment with fully distributed traceback on standard CPU MPI clusters, this work fills a critical gap in high-performance computational genomics.

bioinformatics↗

Pruning the Search, Not the Signal: Adaptive-Banding Needleman-Wunsch via Protein Language Model Confidence

Dynamic programming (DP) yields exact quadratic-time (O(NM)) pairwise sequence alignments. Static banding heuristics (O(NW)) fail catastrophically on low-identity (<30%), asymmetric insertions/deletions (indels), or extreme length ratios, dropping core-block Sum-of-Pairs (SP) score recovery to 20%-50%. Conversely, recent protein language model (PLM) aligners evaluate all N x M cells without search grid constraints. To bridge this gap, we introduce Adaptive-Banding Needleman-Wunsch (AB-NW), pruning the search space without sacrificing sequence alignment signal by leveraging PLM contextual representations to construct a confidence-adaptive DP corridor prior to fine-resolution DP while keeping downstream scoring unmodified. AB-NW downsamples residue embeddings, computes a coarse alignment, and sets per-row corridor bounds via normalized confidence metrics. Evaluated via JIT-compiled buffers, this reduces time complexity to O(NW_bar) and space to O(NW_max), where W_bar << M. Benchmarked across three PLM backbones (ESM2-8M, ESM2-35M, ProtBERT) across nine structural challenge categories, AB-NW recovers >98.9% of exact unconstrained alignment scores and core-block SP accuracy across static banding failure modes (Twilight Zone, Asymmetric Indels, Extreme Aspect Ratios) while eliminating 55.3%-78.8% of active DP cells. On large protein sequence matrices (N, M >= 3,700), AB-NW eliminates 87.6%-91.7% of cells, achieving speedups of 9.79x-13.30x (pure DP) and 1.73x-2.94x (end-to-end), reaching up to 18.12x on unbiased controls (p < 0.05 to p < 10^-15), making AB-NW practical for large-scale, high-throughput sequence alignment pipelines.

bioinformatics↗

Generation, Characterization and Comparison of Ovine Induced Pluripotent and Embryonic-Disc Stem Cells

Pluripotent stem cells derived from livestock species represent valuable systems for studying early mammalian development and for establishing renewable, well-defined cell sources; however, direct comparative characterization of distinct pluripotent stem cell platforms in sheep remains limited. In this study, we established and evaluated two ovine pluripotent stem cell types: reprogrammed induced pluripotent stem cells (siPSCs) and embryonic disc-derived stem cells (sEDSCs). Both siPSCs and sEDSCs exhibited core features of pluripotency, including compact colony morphology, alkaline phosphatase activity, expression of key pluripotency-associated markers, and maintenance of a normal ovine karyotype. Flow cytometry and quantitative RT-PCR analyses revealed broadly overlapping yet distinguishable pluripotency marker expression profiles between the two cell types. Functional pluripotency was confirmed by embryoid body formation and in vitro differentiation into derivatives of all three germ layers. To further assess lineage-specific differentiation competence and compare functional outputs relevant to mesodermal differentiation, both pluripotent stem cell types were directed towards the adipogenic lineage. While siPSCs and sEDSCs were each capable of adipogenic differentiation, differences in differentiation efficiency and marker expression were observed. Together, these findings demonstrate that ovine siPSCs and sEDSCs share core pluripotency characteristics while retaining distinct molecular and functional properties, providing a robust comparative framework for studies of ovine pluripotency, lineage specification, and stem cell biology.

cell biology↗

Single-Nucleus Analysis of Human White Adipose Tissue Reveals Adipocyte Subsets with Distinct Metabolic Profiles

Anatomic location of white adipose tissue is a determinant of cardiometabolic risk. To understand differences within/between adipose depots, we generated 65,668 single-nucleus transcriptomes from human subcutaneous or intraabdominal adipose tissue (SAT/IAT). Unsupervised analysis revealed 26 adipose-resident cell clusters including two subpopulations of mature adipocytes, characterized by high vs. low expression of adipocyte maturation genes (ADIPOMAThi vs. ADIPOMATlo). ADIPOMATlo adipocytes demonstrate a low-differentiation, pro-inflammatory, and pro-fibrotic transcriptome. IAT-resident ADIPOMATlo were more abundant in higher BMI donors, while SAT-resident ADIPOMATlo associated with impaired glycemia. TSHZ3 was identified as a candidate regulator of ADIPOMATlo transcriptome. TSHZ3 knockdown in adipogenic progenitors inhibited differentiation, with downregulation of early adipogenic regulators (e.g. CEBPA/B, PPARG) and mature adipocyte genes. Heterozygous deletion of Tshz3 in mice reduced SAT and IAT weight. Here, we show that adipocyte subsets with distinct transcriptomic signature reside in human WAT; altered TSHZ3-mediated transcriptional regulation may contribute to low-maturation subpopulation linked to metabolic disease.

cell biology↗

Quantitative genetics of photosynthetic trait variation in maize

Natural genetic variation in photosynthesis-related traits can aid both in identifying genes involved in regulating photosynthetic processes and developing crops with improved productivity and photosynthetic efficiency. However, rapidly fluctuating environmental parameters create challenges for measuring photosynthetic parameters in large populations under field conditions. We measured chlorophyll fluorescence and absorbance-based photosynthetic traits in a maize diversity panel in the field using an experimental design that allowed us to estimate and control multiple confounding factors. Controlling the impact of day of measurement and light intensity as well as patterns of two-dimensional spatial variation in the field substantially increased heritability with the heritability of 7 out of 14 traits measured exceeding 0.4. We were able to identify high confidence GWAS signals associated with variation in four spatially corrected traits (the quantum yield of photosystem II, non-photochemical quenching, redox state of QA, and relative chlorophyll content). Insertion alleles for Arabidopsis orthologs of three candidate genes exhibited phenotypes consistent with our GWAS results. Collectively these results illustrate the potential of applying best practices from quantitative genetics research to address outstanding questions in plant physiology and understand the mechanisms underlying natural variation in photosynthesis. Highlights[bullet] Controlling spatial and environmental confounding factors increased heritability of photosynthetic traits. [bullet]GWAS identified high confidence signals associated with variation in relative chlorophyll, {Phi}PSII, {Phi}NPQ, and qL. [bullet]Insertion alleles of the Arabidopsis orthologs of maize candidate genes exhibited photosynthesis related phenotypes consistent with the GWAS results.

plant biology↗

Carbon Dots and Single-walled Carbon Nanotubes Enhances Maize Shading Stress Tolerance

Low sunlight availability/shading stress is one of the major abiotic stresses, limiting plant photosynthesis and biomass production. Maize is a C4 species and requires more sunshine for efficient photosynthesis rate. Thus, maize is a highly shade-sensitive species. We used carbon dots (CDs) and single-walled carbon nanotubes (SWCNTs) as a foliar application to enhance maize photosynthesis under no-shading and shading stress. The results revealed that under shading stress, the higher concentration of CDs and SWCNTs reduced the MDA (Malondialdehyde) content and increased the expression level of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) genes. Moreover, under shading stress, CDs and SWCNTs increased the average thickness of leaf lamina, vascular bundle, mesophyll, and epidermis. CDs and SWCNTs reduced the damaging effects of shading stress on the chloroplast (Ch) formation. CDs and SWCNTs upregulated Rubisco and related genes under shading stress. The chlorophyll fluorescence parameters, including the efficiency of quantum yield of photosystem II (Fv/Fm), electron transport rate (ETR), non-photochemical quenching coefficient (NPQ), and photochemical quenching coefficient (qP) were improved with the foliar application of CDs and SWCNTs under shading stress. Higher stomatal conductance, intercellular CO2 concentration, transpiration, and net photosynthesis were observed in maize plants treated with CDs and SWCNTs under shading stress. The results of our study suggest that using higher concentrations of CDs and SWCNTs can enhance plant growth and photosynthesis under shading stress conditions. However, to avoid nanotoxicity, great care is recommended when selecting different concentrations of nanomaterials based on the growing conditions.

physiology↗

Population level gene expression can repeatedly link genes to functions in maize

Transcriptome-Wide Association Studies (TWAS) can provide single gene resolution for candidate genes in plants, complementing Genome-Wide Association Studies (GWAS) but efforts in plants have been met with, at best, mixed success. We generated expression data from 693 maize genotypes, measured in a common field experiment, sampled over a two-hour period to minimize diurnal and environmental effects, using full-length RNA-seq to maximize the accurate estimation of transcript abundance. TWAS could identify roughly ten times as many genes likely to play a role in flowering time regulation as GWAS conducted data from the same experiment. TWAS using mature leaf tissue identified known true positive flowering time genes known to act in the shoot apical meristem, and trait data from new environments enabled the identification of additional flowering time genes without the need for new expression data. eQTL analysis of TWAS-tagged genes identified at least one additional known maize flowering time gene through trans-eQTL interactions. Collectively these results suggest the gene expression resource described here can link genes to functions across different plant phenotypes expressed in a range of tissues and scored in different experiments.

plant biology↗

Phytochemical and antibacterial analyses of Onychium japonicum (Thunb.) Kunze.

In clinical practice bacterial resistance against antibiotics has become a serious health problem, thus using alternative approaches such as natural products as the supplementary drug could solve it. Therefore, the current study was conducted to thoroughly investigate the enrichment of phytochemicals and antibacterial potential of O. japonicum. The fronds samples of O. japonicum prepared in different solvents were used against MDR bacterial strains and phytochemical analyses. The analyses of data revealed that O. japonicum was enriched with flavonoids, alkaloids, saponins, tannins, glycosides, carotenoids, terpenoids, phlobatanins, phenols, and coumarins while quantitatively this plant has a significantly higher content of phenols(1100.91{micro}M/g) followed by sugar contents (748.67{micro}M/ml), ascorbic acid (426.12mM/g), flavonoids (160.65mg/g), anthocyanin (101.06{micro}M/g) and proline (80.58{micro}M/g). On the other hand, the organic extracts of O. japonicum were highly active against all bacterial strains while hydric extract was inactive against selected bacteria. Specifically, O. japonicum was highly active against S. aureus in all organic extracts (chloroform=16.66{+/-}0.33, ethyl acetate=15{+/-}0.57, methyl alcohol= 14{+/-}0.57, N-hexane=20.33{+/-}0.33) followed by K. pneumonia (chloroform=14.33{+/-}0.33, ethyl acetate=4.33{+/-}4.33, methyl alcohol=3.66{+/-}3.66, N-hexane=16.66{+/-}0.33) and P. aeruginosa (chloroform= 8.33{+/-}4.17, ethyl acetate=8.33{+/-}4.17, methyl alcohol=6{+/-}3.00, N-hexane=9.33{+/-}4.66), while E. coli (chloroform=0{+/-}0.00, ethyl acetate=7{+/-}3.51, methyl alcohol=3.33{+/-}3.33, N-hexane=4{+/-}4.00). Based on current findings it is concluded that O. japonicum is enriched in many useful phytochemicals that could be use as a supplement with other traditionally used antibiotics.

microbiology↗