0% Complete
صفحه اصلی
/
4th international edition and 13th Iranian Conference on Bioinformatics
Dissecting the genetic causes of inflammatory bowel disease based on whole exome sequencing
نویسندگان :
Amir Shahbazi
1
Mehdi Totonchi
2
1- Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
2- Medical Genetics and Molecular Biology Research Hub, Royan TuCAGene Ltd., Tehran, Iran.
کلمات کلیدی :
Inflammatory Bowel Disease (IBD)،Whole-Exome Sequencing (WES)،Gene Variant،Novel Mutation
چکیده :
Introduction IBD refers to the chronic inflammatory diseases of the gastrointestinal tract and mainly encompasses Crohn's disease (CD) and ulcerative colitis (UC). While genetic susceptibility is a major factor in the pathogenesis of IBD, the identification of casual gene variants remains challenging because the disease is heterogeneous. Whole-exome sequencing is an effective approach for identifying rare and novel variants in coding regions ,providing critical insights into the genetic architecture of complex diseases like IBD. Methods This study aimed to identify new genetic variants associated with IBD using WES in one family with familial IBD. We analyzed 5 person,3 was affected and 2 person was healthy, using high-throughput WES technology, Data processing involved quality control and trimming , alignment to the reference genome (GRCh37) using hisat2 , and for variant calling using GATK toolkit. Results We identified a novel frame shift variant in FCGBP Gene (NM_003890.2:chr19-40399459 TG>T, p.His2079Ilefs*20) . gene implicated May be involved in the maintenance of the mucosal structure as a gel-like component of the mucosa. This variant exhibited in one of patient in family of under study that show strong connection with IBD and was absent in healthy controls. Conclusion These findings demonstrate the use of WES in identifying the genetic causes of IBD and emphasize the role of GeneFCGBP in the development of IBD. This discovery opens up new possibilities for the identification of the mechanisms of disease, the development of new therapies and the advancement of precision medicine in the treatment of IBD patients.
لیست مقالات
لیست مقالات بایگانی شده
Diabetes nephropathy indicators for early diagnosis
Sedigheh Momenzadeh - Masumeh Jalalvand - Reza Nedaeinia
BiogenExplorer: A Robust Solution for Rapid Gene Presence Detection and Allelic Diversity Analysis in large Genomic Datasets
Mohammadreza Najafi Disfani - Danial Ghofrani - Mahdiar Mansouri - Parastoo Saniee
Applying immunoinformatics methods using gb41 and gp120 genes of HIV virus to design a multi-epitope vaccine
Zahra Hassanzadeh - Fatemeh Hassanzadeh - Ava Hashempour
Physical parametric study of bacterial biofilm disruption and removal by jet impingement: A CFD investigation
Fatemeh Ebrahimi Tarki - Mahboobeh Zarrabi - Mahkame Sharbatdar - Ahya Abdi Ali
The Regulatory Role of DNA Methylation in Age-Related Macular Degeneration (AMD)
Shohreh Yazdani - Alireza Fotuhi Siahpirani
Targeting Protein in Neurodegenerative Diseases: A Computational Approach
Reyhaneh Ebrahimi - Seyed Hassan Alavi - Fayaz Soleymani - Fatemeh Zare-Mirakabad
Investigating the role of ursolic acid in EGFR L858R mutant inhibition in non-small cell lung cancer: Molecular docking and ADMET prediction
Tooba Abdizadeh
Exploring the Anticancer Potential of Flavonoids from Morus alba Against Breast Cancer: An In Silico Approach
Kimia Asadi - Negar Ghaleh Navi - Ehsan Karimi
Towards Efficient Recombinant Protein Production: In-silico screening of signal peptides for secretory production of recombinant factor C in mammalian cells
Maryam Latifi - Kosar Asadi - Mansoureh Shahbazi Dastjerdeh
HLA Class I Alleles as prognostic marker in Hepatocellular Carcinoma
Shahram Aliyari - Zahra Salehi - Mohammad Hossein Norouzi-Beirami - Kaveh Kavousi
بیشتر
ثمین همایش، سامانه مدیریت کنفرانس ها و جشنواره ها - نگارش 42.7.0