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Biology subjects

Gul, R.

Publications and source records attributed to Gul, R..

2 recordsLinked to original sources

GenoSim: A Forward-Time Genotype Simulator for Clinical and Population Genetics with Population Stratification

MotivationNext-generation sequencing studies in clinical genetics are often limited by the scarcity of human genotype data, which stems from ethical, regulatory, and economic barriers. The shortfall is sharpest in consanguineous populations, which are common in South Asia and the Middle East, where family-based designs need large pedigrees that are rarely sequenced in full. Existing simulators do not combine pedigree-aware propagation, realistic population stratification, and clinical export formats in one tool. ResultsWe present GenoSim, an R package for forward-time simulation of diploid SNP genotypes. It runs in two modes: a population mode implementing inbreeding-adjusted Hardy-Weinberg sampling, Wright-Fisher drift, directional selection, recurrent mutation, and Haldane recombination across multiple generations; and a pedigree-constrained mode that ingests real family VCFs and a pedigree, reconstructs phase where the pedigree makes it identifiable, propagates genotypes through the observed family structure, and appends synthetic generations. Version 1.1.1 adds population stratification through the Balding-Nichols model parameterised by gnomAD v3.1 fixation indices (Fsr) for eight ancestry groups (AFR, AMR, EAS, EUR, FIN, MID, SAS, ASJ), empirical allele-frequency loading from external reference panels, and admixed-cohort simulation. Analysis functions cover Hardy-Weinberg testing, linkage disequilibrium, runs of homozygosity, principal component analysis, founder-referenced and between-generation F-statistics, and Nei gene diversity. Output is compatible with VCFv4.2, PLINK PED/MAP/RAW, and tidy CSV. Availability and implementationGenoSim is available as an R package at https://github.com/malikbak/GenoSim under the MIT licence. It requires R [≥]4.0.0 and depends only on base R packages (stats, utils, graphics, grDevices, tools). Contactmalikabubakar279@gmail.com

bioinformatics↗

Mutation in DsbA signal sequence hampers the SRP mechanism: A new strategy to combat virulence factor

Disulphide bond (Dsb) protein, characterized as an important virulence factor in gram negative bacteria. In this study, amino acid mutations in DsbA signal sequence (ss) and its effect on translocation of recombinant Ovine growth hormone (rOGH) was observed. Eight constructs were designed on the basis of increased hydrophobicity and showed that hydrophobicity and specificity of amino acid plays a crucial role in translocation of rOGH. Two DsbAss with the same hydropathy (1.539), one had alteration at -13 and second at -11 position; alanine (Ala) to isoleucine respectively were designed. The former DsbAss translocated rOGH from membrane to cytoplasmic fraction in E. coli as confirmed by SDS-PAGE, Western blot and molecular modelling analysis. MD simulations and binding free energy calculations evidenced that, altering Ala changed the orientation of signal peptide in the Ffh-M domain binding groove and hampered the process of translocation while change at position -11 pointed it outward. We hypothesize, amino acid and position of mutations in DsbAss can hinder the translocation process of signal recognition particle system, thus affecting the virulence of bacteria.

bioengineering↗