Forough Sadeghipour

I completed my bachelor's degree in Cellular and Molecular Biology, where I developed a solid foundation in biological concepts and techniques. During my studies, I discovered a deep fascination for the field of bioinformatics and its potential to revolutionize personalized medicine. To further pursue this passion, I obtained a master's degree in Human Genetics, focusing on molecular diagnostic methods and their applications in genetic diseases. Through my master's thesis project, I successfully identified novel mutations and a minisatellite marker in the CTNS gene associated with Infantile Nephropathic Cystinosis, demonstrating my ability to contribute to the understanding of genetic disorders. In recent years, I have expanded my expertise to encompass cutting-edge technologies such as RNA sequencing data analysis and whole exome sequencing data analysis. I have developed proficiency in utilizing R programming to process and analyze vast quantities of genomic data, extracting meaningful insights from complex datasets. My skills in statistical analysis, data visualization, and command line tools have allowed me to uncover valuable information from high-throughput sequencing data, contributing to the identification of differentially expressed genes in cancers. My experiences working as a Whole Exome Sequencing data analyst at Comprehensive Medical Genetic Center have further enhanced my bioinformatics skills and provided me with a comprehensive understanding of the field. Moreover, I have over five years of experience working in cytogenetic and Molecular laboratories, where I am trained in various techniques such as cell culture, FISH study, microscopy and qPCR. Throughout my academic and professional journey, I have demonstrated exceptional work ethics and the ability to work both independently and collaboratively within diverse teams. I am eager to contribute my expertise and passion to your research projects. Additionally, my strong background in human genetics provides me with a unique perspective, enabling me to approach personalized medicine research with a deep understanding of the underlying genetic mechanisms. I am confident that working alongside esteemed researchers and collaborating with fellow passionate scientists will provide an ideal environment for me to further expand my knowledge and contribute to groundbreaking discoveries.

Living in : Iran

Gender : FemaleRace : Middle Eastern

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Academic Profile

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Contact Information

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Educations

Human GeneticsMaster'sShiraz University of Medical Sciences2016-07-19 Iran

Supervisor's name :Dr. Majid Fardaei

Title :

CTNS gene mutation analysis in 20 unrelated Iranian families with cystinosis.

cellular and molecular biologyBachelor'sShahrekord University2012-07-20 Iran

Work Experiences

Molecular genetic technic

at Comprehensive Medical Gen

I am currently working in this role

Cytogenetic technician

at Faghihi’s Genetic Center

Start : 01-Feb-2017

End : 27-Jun-2022

English Scores

Doulingo22-Dec-2022

120/160Total

Conferences

Your Presentation Title :

Characterization of the Most Common Mutation in CTNS gene in Iranian Patients with Infantile Nephropathic Cystinosis

Conference Name :Pediatric Nephrology

Iran

2016

Your Presentation Title :

Evaluation of Heterozygosity Degree of a New Identified Minisatellite Marker at the CTNS Gene

Conference Name :Iranian Genetics Congress

Iran

2016

Journal Publications

Publication Title :

A Novel TTC19 Mutation in a Patient with Neurological, Psychological, and Gastrointestinal ImpairmentCorresponding author

Journal :

Frontiers in Neurology

Link :

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Publication Title :

A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case reportCorresponding author

Journal :

BMC Medical Genetics

Link :

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Publication Title :

Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutationsFirst author

Journal :

Human Genome Variation

Link :

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Research Keywords

non-coding RNA

cancer

Whole Exome Sequencing data analysis

CRISPR/ Cas9

Stem cell studies

RNA-seq data analysis