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USD 70 /hr
Hire Dr. Anamika G.
Germany
USD 70 /hr
Bioinformatician with 10 years of experience in NGS ,single cell MultiOmics, Deep learning
Profile Summary
Subject Matter Expertise
Services
Research
Scientific and Technical Research
Consulting
Healthcare Consulting,
Scientific and Technical Consulting
Data & AI
Statistical Analysis,
Algorithm Design-ML,
Data Processing
Work Experience
Staff Scientist, Computational Biology
Max Delbrück Center for Molecular Medicine
January 2025 - November 2025 ![]()
Bioinformatics Scientist
BIH Center for Regenerative therapies & Charité
May 2021 - October 2024 ![]()
Postdoctoral Resaercher
Berlin Institute of Health at Charité - Universitätsmedizin Berlin
May 2018 - May 2019 ![]()
Doctoral student
Hertie Institute for Clinical Brain Research
March 2015 - February 2018 ![]()
Bioinformatician
Universitätsklinikum Düsseldorf
November 2012 - November 2014 ![]()
Education
Doctorate
Eberhard Karls Universität Tübingen
March 2015 - February 2018 ![]()
Masters of Science
University of Bonn
October 2009 - May 2012 ![]()
Bachelors of Technology
Dr. D. Y. Patil Biotechnology & Bioinformatics Institute
July 2004 - June 2008 ![]()
Certifications
Publications
JOURNAL ARTICLE
Krieger TG, Le Blanc S, Jabs J, Ten FW, Ishaque N, Jechow K, Debnath O, Leonhardt CS, Giri A, Eils R, et al. (2021). Single-cell analysis of patient-derived PDAC organoids reveals cell state heterogeneity and a conserved developmental hierarchy . Nature communications.
Giri A, Mok KY, Jansen I, Sharma M, Tesson C, Mangone G, Lesage S, Bras JM, Shulman JM, Sheerin UM, et al. (2016). Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population . Neurobiology of aging.
Giri A, Guven G, Hanagasi H, Hauser AK, Erginul-Unaltuna N, Bilgic B, Gurvit H, Heutink P, Gasser T, Lohmann E, et al. (2016). PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism . Tremor and other hyperkinetic movements (New York, N.Y.).
Hanagasi HA, Giri A, Kartal E, Guven G, Bilgiç B, Hauser AK, Emre M, Heutink P, Basak N, Gasser T, et al. (2016). A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family . Parkinsonism & related disorders.
Daschkey S, Röttgers S, Giri A, Bradtke J, Teigler-Schlegel A, Meister G, Borkhardt A, Landgraf P (2013). MicroRNAs distinguish cytogenetic subgroups in pediatric AML and contribute to complex regulatory networks in AML-relevant pathways . PloS one.