Current position:
I am a bioinformatician who holds a PhD in bioinformatics along with a background in molecular genetics, a BSc, and a MD. I am currently working on some projects with Professor Abd El-Nasser Khattab at National Research Center - Egypt, Director of the Biotechnology Research Institute's Genetics and Cytology Department.
Research Interesting and experience:
I am so interested in applying eDNA plus bioinformatics to the ecology in general but I am so fascinated to utilize the bioinformatics methods and computational tools to microbial communities in marine.
In my current position, I am a researcher and bioinformatician (minor specialist metagenome and genome big data analysis) who holds a PhD in genetic engineering and bioinformatics in combination with a background in molecular genetics, a BSc and a MD, working with Professor Abd El-Nasser Khattab at the National Research Center - Egypt on some projects related to marine microbiology, Professor Abd El-Nasser Khattab is the Director of the Genetics & Cytology Department at the Biotechnology Research Institute.
I am so fascinated by the bioluminescent field and two years ago I decided to apply for a master degree of biological engineering at Siberian Federal University under the supervision of Prof. Dr. Valentina A. Kratasyuk, Professor, Head, Department of Biophysics, Siberian Federal University but for some personal issues I returned again.
I am preparing a bioluminescence unit to detect the low level of heavy metal in the environment and effect of nanoparticles on the environment and making biomeasure for the glow that emitted via the bioluminescent bacteria using the Glow-Max system of Promega - USA.
After returning to Egypt I triggered myself by searching for a new host in our Egyptian environment on the Red Sea Coast. I brought some squid individuals and with a cooperation with Dr. Nasser we succeeded in isolating strains from two regions of the squid (Ink sack and Eye).
Then we made a pure single colony from the plates and we sent a liquid culture to a genomic service lab to have the WGS of the bioluminescent strain utilizing Nanopore sequencing. I used my bioinformatics experience to assemble and polishing the genome then annotate the genome but through the Bandage tool I detected two circular genomes (First node = 4,992,825 bp and Second node = 3,256,386 bp).
1. Shewanella 2024
https://www.ncbi.nlm.nih.gov/nuccore/AP031461
2. Psychrobacter 2024
https://www.ncbi.nlm.nih.gov/nuccore/AP031495.1
I have strong experience in generating command lines to build a metabarcoding pipeline analysis (Bashes) using different tools and linux command lines (Usearch - Vsearch - Classification tool kraken - Assigning taxonomy - abundance analysis using DADA2 whole pipeline and QIIME 2 whole pipeline, whether long reads or short reads).
Solid experience in bacterial genome assembly and annotation (short - long, reads), comparative genome , finding similar genome, phylogenomic tree and synteny gene detection.
I am so interested in analyzing the mtDNA and cpDNA of plants and finding the genetic markers inside the whole genome of plant organelle in PhD I programmed a tool named RFRE tool-(https://sourceforge.net/projects/rfret/) to find the LTR markers and SSR markers in the date palm trees in our desert utilizing the regular expression language.
The tool is programmed by visual basic language and regular expression language.
I have a solid experience in data processing for the DNA barcoding genes and annotation of the processed data to submit the information to BOLD database or to DDBJ or NCBI.
I have experience in analyzing the DNA barcoding genes of desert plant (Egyptian olive cultivars)and building phylogenetic tree by using different tree construction algorithms.
International advanced training course in Bioinformatics:
Genomic prediction and selection in plant breeding, international centre for advanced mediterranean agronomic studies, Mediterranean agronomic institute of Zaragoza, Spain 40 hrs,16-28 January 2016.
Applications of bioinformatics in plant breeding, international centre for advanced Mediterranean agronomic studies, Mediterranean agronomic institute of Zaragoza, Spain 36 hrs, 18-22 January 2014.
My goal is to grow my publication portfolio and advance my career in bioinformatics applications to ecology.
Develop applications for non-routine measurements in support of new products and business development (Promega Life Science Department) and Loewe products of plant molecular diagnostic kits
Install and conduct sample handling, measurements, and data analysis of Molecular Diagnosis kits (Real-Time PCR 48-4 channel by BIORON-Germany).
Conduct sample handling, measurements, and data analysis, including molecular biology techniques and PCR | Real time PCR | Cloning Kits | DNA / RNA from different resources | HMW DNA kits from different resources |Plant diseases molecular diagnostic kits of Loewe
Design experiments to test hypotheses or demonstrate the feasibility of a new application, or provide proof of concept to a customer
Create documents such as application notes, technical notes, and support the creation of new marketing material.
Provide installation and training support for customers.
Perform demonstrations and user training in the field.
Data Processing and Analysis (Marine Bioluminescence Microbiome of Cephalopod):
Preprocessing and Quality Control: Help clean and organize raw metagenomic sequencing data before analysis. This could involve tasks like adapter trimming, quality filtering, and checking for contamination.
Assembly and Annotation: Assembling metagenomic reads into contigs (contiguous sequences) and annotating genes within those contigs. This might involve using tools like metaSPAdes or Flye for Long Reads.
Community Profiling: Contribute to projects that aim to identify and characterize the different microbial communities present in a metagenomic sample. This could involve using software like QIIME2 or Kraken2.
Functional Analysis: Help researchers understand the functional potential of a microbial community by analyzing predicted protein sequences or metabolic pathways. This might involve using databases like KEGG or searching for specific genes of interest.
Courses (Bioinformatics tools and Pipeline - Basic programming - Genetic population - Biostatistics).
Evaluated student progress through regular assessments, providing detailed feedback for improvement and growth.
Created and designed quizzes, tests and projects to assess student knowledge.
Developed strong relationships with colleagues, collaborating on curriculum development and sharing best practices in teaching strategies.
Developed and implemented innovative teaching strategies to engage students in lectures and coursework.
Participating in the training courses and workshops of bioinformatics and molecular genetics.
Bioinformatics analysis (Pre-genomics, PCR Insilco, Primer design, Blasting, Quality control of chromatogram curve of Sanger method, fragments assembly, genomic analysis, constructing the Phylogenetic tree and Genban submission)
Bioinformatician and Biologist
eDNA and Molecular Ecology Lab
LAKES & FISH RESOURCES PROTECTION & DEVELOPMENT AGENCY (LFRPDA)
Updating and modifying methods of DNA isolation and supervising research services offered by the Lab.
Determining methods of isolation of fish DNA and studying its water environment.
Classifying and studying invasive species of water environment in Egypt through DNA Barcoding Gene and Genetic Monitoring for Invasive Species.
Making studies of water quality analysis (DO, pH, salinity, Spectrophotometers from heavy metal, turbidity and TDS).
Writing environmental reports on the results of water quality for fish farming and making environmental studies on the basis of the reports.
Classifying and studying invasive species of water environment in Egypt through DNA Barcoding Gene and Genetic Monitoring for Invasive Species.
Conducting DNA test as a genetic sequence through bioinformatics pipeline analysis tools or R packages.
Preparing and developing the material and methods for the research tasks.
Training the undergraduate students on the molecular genetics techniques, Bioinformatics (Dynamic array programs) and Pairwise alignment theory and application of gene predication.
Design the experiments of molecular techniques , DNA Isolation from Different species , RNA, Protein , PCR reaction , Cloning, Real time PCR and qPCR analysis.
Analyzing, annotating and submitting the sequenced genes from differentorganisms Bacteria, Fungi, Animals , Plants to the Gene bank.
Designing and doing the microbial genetics research experiments.
Participating in the training courses and workshops of bioinformatics and molecular genetics.
Participate on the scientific conferences and sharing with a scientific paper.
Gel documentation analysis for DNA and Protein fingerprinting techniques.
Writing the research reports and Scientific report to the lab directors.
Designing and doing the microbial genetics research experiments.
Bioinformatics analysis (Pre-genomics, PCR Insilco, Primer design, Blasting, Quality control of chromatogram curve of Sanger method, fragments assembly, genomic analysis, constructing the Phylogenetic tree and Genbank
submission).
Making the biostatics analysis for the researcher as lab services using SPSS and Excel sheet.
Training the lab technician to run the devices inside the research lab.
Writing and publishing the research papers on the peer review journals.
Teaching the genomic analysis courses and bioinformatics for the undergraduate students (Biostatistics, Genetic population, Genome analysis
and Bioinformatics).
Laboratory skills
Symposium power of viruses, 05/16/2018, Croatia, Retrieving a Tandem Repeats Motif in the Completed Genomes of Human Coronavirus (Hku1) Which Identified as a HotSpot Region for the Virus Recombination by Using Regular Expression Language
A. I'm very interested in using my programming skills in solving biological problems. I programmed a mini tool to find the SSR and LTR sequences in the organelle genomes and viruses genome RFRE, ( https://sourceforge.net/projects/rfre) .
B. I design a workflow to analyze the metabarcoding genes for NGS data paired end to produce Merging pair-end reads, quality filtering, de-noise, OTU curation, and taxonomic assignment utilizing https://github.com/ezzbioinf/Marine-environmental-DNA-metabarcoding-data-analyses-practical-11-13-October-2023
C. I have experience in utilizing bioinformatics tools, utilizing different programming languages (Bioperl- Biopython Data analysis and scripting text files- OOP language object oriented programming language and event driven programming language- RegEX regular expression language - Excel programming - Accesses programming) and database normalization and construction from 0NF level to BCNF level.
D. I have Bioinformatics skills in different areas, pipelines in RNA-seq analysis and de novo assembly.
E. Metagenomic analysis using QIIME 2 and Submitting processed reads to (MG-RAST) pipeline.
F. Metagenomic assembly utilizing metaspades.
G. Metabarcoding pipeline by using R packages DADA2.
H. Metagenomic 16S rDNA and Metagenomic WGS by using R packages. I. Merging pair-end reads, quality filtering, de-noise, OTU curation, and taxonomic assignment utilizing USEARCH algorithm and UBLASTsearch algorithm.
Bioinformatics experience and eDNA/Metabarcoding analysis long reads:
J. Making an Assembly and de novo assembly (short reads and long reads) using different pipeline tools, Mapping and Visualization for high-throughput data, comparison across species and synteny analysis).
K. Genome assembly for long reads which comes out from nanopore , MinION Data utilizing MEGAHIT.
L. Genomic selection pipeline analysis and visualizing SNPs by Flapjack-graphical genotype visualization tool.
M. Comparative genomics by using CoGe server to identify the synteny gene.
N. I am familiar with Aligning genomes (multiple genome alignment) with Mauve tool, The CoGe Comparative Genomics Platform to define synteny genes and YASS genomic similarity search tool.
O. Discover the barcode gap utilizing ASAP (Assemble Species by Automatic Partitioning).
P. I am familiar with NGS pipelines of Data analysis NGS analysis (Quality control for NGS raw data (FASTQ), DNA and RNA-seq NGS read alignment, Variant Calling).
Q. Visualizing SNPs by Flapjack-graphical genotype visualization. R. Multiple genome alignment (GENOMES) by using the MAUVE tool.
Genomic Analysis :
A. NGS analysis (Quality control for NGS raw data (FASTQ), DNA and RNA-seq NGS read alignment, Variant Calling, Making an Assembly and de novo assembly (short reads and long reads) using different pipeline tools, Mapping and Visualization for high-throughput data, comparison across species and synteny analysis).
B. Visualizing SNPs by Flapjack-graphical genotype visualization.
C. Metagenomic analysis and Metabarcoding using QIIME 2 and Submitting processed reads to (MG-RAST) pipeline
D. Metabarcoding using 12s barcode gene to make biodiversity assessment for fish stock.
E. Metabarcoding analysis using R packages and DADA2 and Excel macros.
F. Metabarcoding analysis utilizing Usearch and Vsearch from OTU to downstream analysis (Alpha and Beta
Diversity).
G. Utilizing Kraken2 and Krona tools in assigning taxonomy and taxonomy visualization.
H. Metabarcoding pipeline analysis for long reads assembly of raw data produced by Nanopore Oxford.
I. Bacterial genome assembly and data annotations - mtDNA assembly and cpDNA assembly using Flye - Canu - Spades - Megahit.
J.Comparative genomics by using CoGe server to identify the synteny gene.
K.I am familiar with Aligning genomes (multiple genome alignment) with Mauve tool, The CoGe Comparative Genomics Platform to define synteny genes and YASS genomic similarity search tool.
L.Multiple genome alignment (GENOMES) by using the MAUVE tool.
Computer skills :
A. (Descriptive Analysis, Comparative Analysis, Experimental Design, GLM Modules) by using SPSS and Excel.
B. LINUX, command lines and shell scripts, Bioperl and Python programming language in genomic data analysis and visualization.
C. System analysis and Database Normalization (0NF to BCNF).
D. Oracle for PC’s (RDBMS, SQL, SQL*PLUS). E. MS-Visual Basic 6.0.
Phylogenetic tree analysis:
A. Data preparation.
B. Phylogenetic inference based on distance methods.
C. Phylogenetic inference using maximum likelihood methods.
D. Phylogeny inference based on parsimony and other methods.
E. Estimating selection pressures on alignments of coding sequences (dn/ds).
F. Testing topology.
G. Bootstrapping analysis to produce a confidence tree.
H. Using the suitable Substitution model to construct the phylogenetic tree.
I. Choose the corrected algorithm to construct the phylogenetic tree and change the option of clustalw algorithm to optimize the tree topology.
Molecular Biology skills:
A. Experience in lab techniques (DNA isolation, RNA isolation from different sources , Bacterial cells, Plant tissue, cell culture, fishes,Blood)
B. SDS-PAGE,
C. Degenerate PCR protocol
D. Long PCR protocol
E. RT/PCR, Real time PCR, ΔΔcT Calculation for comparative genomic expression).
F. DNA / RNA isolation protocols
G. Cloning protocols H. Molecular taxonomy by using DNA barcoding gene and Insilco pipeline analysis to construct phylogenetic tree. I. Real time PCR experiment by using SYBR green dye and Calculating the ΔΔCt value. J. Microbial ecology and molecular diagnostics.
2019 PhD is Verified International Academic Qualifications Issued by World Education Services (WES), https://wes.credly.com/member-badges/20370073.
2024 PhD is Verified International Qualifications Recognition Statement (NZQA), NZQA Application Number: 092897