I have an extensive experience in use of bioinformatics tools for analysis and integration of large-scale data. With a particular focus on DNA variant annotation and expression quantitative trait loci eQTLs analysis, miRNA targets predictions, transcriptome and methylome analyses of results obtained from Next Generation Sequencing NGS.
In my work, I use fluently highly sophisticated computer programs, statistical knowledge and I’m very familiar with operating several databases. I am able to use diverse bioinformatics methods to integrate different studies and determine networks between gene sets to develop a new hypothesis and new research avenues. I'm always putting special emphasis on the data visualization.
Linux, R, Galaxy, Cytoscape, Genespring, Pathway Architect, Ariadne Pathway Studio, Ingenuity Pathway Studio, GraphPad, EndNote, StrandNGS software Avadis, SeqMonk
Databases: GTEx, Discovehr, Ensembl, Panther, GeneMania, KEGG, GEO, DrugBank etc.
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