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massiddamt/README.md

Hi there, I'm Matteo 👋

I am a bioinformatician and work in Sardinia (Italy).

I started my academic career as a molecular biologist, dealing with the study of DNA using common techniques such as extraction, PCR, RFLP, Sanger sequencing and NGS.

I have subsequently undertook training that has led me into bioinformatics for the past 8 years. Mainly I have been involved in the analysis of NGS data and, most importantly, the development of scalable and reproducible bioinformatics analysis workflows. To do this I used the workflow manager Snakemake.

As a result, previous work experience at CRS4 led to the creation of a set of publicly available bioinformatics pipelines encapsulated in the solida-core collection.

Since 2022 I have been working at the University of Sassari (Department of Medical, Surgical and Experimental Sciences) and in collaboration with some colleagues at the IRGB-CNR in Cagliari we have created a new collection of reproducible pipelines available on github at the following link: GeneBANGS.

The main project I am actually focused on is the analysis of the transcriptome of CRC patients for the identification of prognostic markers.

If you are interested in a collaboration please do not hesitate to contact me with an email to mmassidda@uniss.it.

Thanks,

Matteo

Pinned

  1. rna_vc_docker rna_vc_docker Public

    A Snakemake pipeline for RNA Seq Variant Calling

    Python 2

  2. GeneBANGS/RNASeq GeneBANGS/RNASeq Public

    A Snakemake pipeline for RNASeq data analysis

    Python

  3. solida-core/musta solida-core/musta Public

    MUSTA: a modular pipeline to detect, classify and interpret mutations in cancer

    Python

  4. solida-core/diva solida-core/diva Public

    DiVA (DNA Variant Analysis) is a pipeline for Next-Generation Sequencing Exome data anlysis

    Python 6