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Profile Details
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USD 80 /hr
Hire Milad E.
France
USD 80 /hr
+9 years of experience in clinical research, Java programmer, NGS data analyst, AI-based application developer
Profile Summary
Subject Matter Expertise
Services
Writing
Medical Writing,
Audio Transcription,
General Proofreading & Editing
Research
Meta-Research,
Gray Literature Search,
Scientific and Technical Research,
Systematic Literature Review
Data & AI
Data Visualization,
Big Data Analytics,
Text Mining & Analytics,
Data Mining,
Data Cleaning,
Data Processing
Work Experience
Research Engineer
Institut de Génétique Humaine
April 2025 - Present ![]()
CEO and instructor
AD bioinformatics
September 2016 - Present ![]()
Remote Bioinformatics Analyst
McGill University
March 2024 - December 2025 ![]()
Clinical WES data analyst
MOM fertility and infertility center
January 2022 - April 2022 ![]()
Analyst and PCR technician
Payvand medical and specialty laboratory
October 2018 - March 2021 ![]()
Lab technician
Hazrat Rasoul Akram Hospital
September 2014 - September 2016 ![]()
Education
Masters of Science
Tarbiat Modares University
January 2016 - January 2019
Bachelor of sciences (Paramedical sciences department)
Babol University of Medical Science
October 2010 - July 2014 ![]()
Certifications
- Certification details not provided.
Publications
JOURNAL ARTICLE
Milad Eidi, Tohid Ghasemnejad, Yuheng Liang, Khadijeh Hoda Jahanian, Arash Salmaninejad, Seyedeh Sedigheh Abedini, Fabrizzio Horta, Nigel H Lovell, Thantrira Porntaveetus, Mark Grosser, et al. (2026). Comprehensive Evaluation of ACMG/AMP-based Variant Classification Tools . Bioinformatics.
Milad Eidi, Gaoussou Sanou, Guilhem Zeitoun, Taciana Manso, Shamsa Batool, Anjana Kushwaha, François Grand, Myriam Croze, Axel Vaillant, Chahrazed Debbagh, et al. (2026). IMGT® at scale: FAIR, dynamic, and automated tools for immune locus analysis . Nucleic Acids Research.
Milad Eidi, Mohsen Yari, Mohammad-Amin Omrani, Zahra Fazeli, Mohammad Rahmanian, Soudeh Ghafouri-Fard (2025). Comprehensive identification of hub mRNAs and lncRNAs in colorectal cancer using galaxy: an in silico transcriptome analysis . Discover Oncology.
Eidi, M., Abdolalizadeh, S., Moeini, S., Garshasbi, M., Zahiri, J.(2024). 123VCF: an intuitive and efficient tool for filtering VCF files . BMC Bioinformatics. 25. (1).
Milad Eidi, Mehrdad Mohammadi, Mahmood Saffari, Seyed Davar Siadat, Seyed Hossein Hejazi, Mohammad Shayestehpour, Mitra Motallebi(2023). Isolation, characterization, therapeutic potency, and genomic analysis of a novel bacteriophage vB_KshKPC-M against carbapenemase-producing Klebsiella pneumoniae strains (CRKP) isolated from Ventilator-associated pneumoniae (VAP) infection of COVID-19 patients . Annals of Clinical Microbiology and Antimicrobials. 22. (1). Springer Science and Business Media {LLC}
Mohammadi, M., Saffari, M., Siadat, S.D., Hejazi, S.H., Shayestehpour, M., Motallebi, M., Eidi, M.(2023). Isolation, characterization, therapeutic potency, and genomic analysis of a novel bacteriophage vB_KshKPC-M against carbapenemase-producing Klebsiella pneumoniae strains (CRKP) isolated from Ventilator-associated pneumoniae (VAP) infection of COVID-19 patients . Annals of Clinical Microbiology and Antimicrobials. 22. (1).
Milad Eidi (2020). Novel neuroclinical findings of autosomal recessive primary microcephaly 15 in a consanguineous Iranian family . European Journal of Medical Genetics.
Milad Eidi (2020). Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS . European Journal of Human Genetics.
Garshasbi, M., Mahmoudi, M., Razmara, E., Vojdanian, M., Aslani, S., Farhadi, E., Jensen, L.R., Arzaghi, S.M., Poursani, S., Bitaraf, A., et al.(2020). Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS . European Journal of Human Genetics. 28. (6). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 754-762.
Razmara, E., Azimi, H., Tavasoli, A.R., Fallahi, E., Sheida, S.V., Eidi, M., Bitaraf, A., Farjami, Z., Daneshmand, M.A., Garshasbi, M.(2020). Novel neuroclinical findings of autosomal recessive primary microcephaly 15 in a consanguineous Iranian family . European Journal of Medical Genetics. 63. (12).
Milad Eidi (2019). A novel ISCA2 variant responsible for an early-onset neurodegenerative mitochondrial disorder: a case report of multiple mitochondrial dysfunctions syndrome 4 . BMC Neurology.
Eidi, M., Garshasbi, M.(2019). A novel ISCA2 variant responsible for an early-onset neurodegenerative mitochondrial disorder: A case report of multiple mitochondrial dysfunctions syndrome 4 . BMC Neurology. 19. (1).
PREPRINT
Milad Eidi, Samaneh Abdolalizadeh, Mohammad Hossein Nasirpour, Javad Zahiri, Masoud Garshasbi (2024). 123FASTQ: an intuitive and efficient tool for preprocessing Illumina FASTQ reads .
Samaneh Abdolalizadeh, Mohammad Hossein Nasirpour, Javad Zahiri, Masoud Garshasbi, Milad Eidi (2024). 123FASTQ: an intuitive and efficient tool for preprocessing Illumina FASTQ reads .