Developing the project "Multi-tool integration for comprehensive characterization and validation of genomic and transcriptomic data" (expected Nov 2025)
Focus on automated pipelines for WGS and RNAseq data, integrating multiple variant callers to improve genomic analysis accuracy.
Contributed to EU-funded projects (GenomePT, MISTiC)
Supported development of computational workflows for high-throughput sequencing data analysis.
Developed and optimized bioinformatics pipelines within the national GenomePT project
Supported cancer genomics and rare disease research.
Marta Ferreira, MSc is a PhD candidate in Bioinformatics in Health, with over seven years of research experience in genomics, transcriptomics, and bioinformatics tool development. Her work focuses on designing and implementing automated pipelines for whole-genome sequencing (WGS) and RNAseq data, integrating multiple variant callers to improve accuracy and reproducibility. She has contributed to several national and European research projects in cancer genomics, rare diseases, and precision medicine, including SOLVE-RD, LEGOH, MISTiC, and GenomePT.
She has co-authored 13 peer-reviewed publications in international journals such as Gut, Brain Communications, and Gastric Cancer. In addition to her research, she actively teaches and mentors students, and has organized multiple workshops and PhD training sessions on bioinformatics and omics data analysis.
Her strengths include technical innovation, analytical problem-solving, and collaborative research across computational and experimental teams, making her a versatile and motivated bioinformatician with a strong commitment to scientific excellence.
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