Pinned Repositories
Codecademy_projects
Python: Repository of small projects done in python through Codecademy
DNA_fragment_analysis_automatisation
UNIX and R: Code to automatically analyze dna fragment from COBRA experiments run on fragment analyzer
Graceffo_et_al_2024_IJMS
R: This repository contains the R code used to run DE analysis and generate plots of the publication "RNA-sequencing of healthy adult human tissues reveals differential splicing of Thyroid Hormone Receptor alpha"
MSc_Neuroscience_TT2020
R: Alternative Splicing Analysis of IPSCs-derived dopaminergic Neurons This repository contains all the R scripts used for the reasearch project carried out during Trinity Term 2020 in Richard Wade-Martins lab
NGS_Oncology_Data_Analysis
R: Example of data analysis of Next Generation Sequencing datasets. I assessed the impact of different starting amounts of DNA and different percentages of Tumor vs Control on the quality of Single Nucleotide Variation (SNV) and somatic allele frequency detection
MSc_TT2020
eugeniograceffo's Repositories
eugeniograceffo/Codecademy_projects
Python: Repository of small projects done in python through Codecademy
eugeniograceffo/DNA_fragment_analysis_automatisation
UNIX and R: Code to automatically analyze dna fragment from COBRA experiments run on fragment analyzer
eugeniograceffo/Graceffo_et_al_2024_IJMS
R: This repository contains the R code used to run DE analysis and generate plots of the publication "RNA-sequencing of healthy adult human tissues reveals differential splicing of Thyroid Hormone Receptor alpha"
eugeniograceffo/MSc_Neuroscience_TT2020
R: Alternative Splicing Analysis of IPSCs-derived dopaminergic Neurons This repository contains all the R scripts used for the reasearch project carried out during Trinity Term 2020 in Richard Wade-Martins lab
eugeniograceffo/NGS_Oncology_Data_Analysis
R: Example of data analysis of Next Generation Sequencing datasets. I assessed the impact of different starting amounts of DNA and different percentages of Tumor vs Control on the quality of Single Nucleotide Variation (SNV) and somatic allele frequency detection