Author

Marcella Attimonelli

University of Bari Aldo MoroORCID 0000-0003-2091-8364Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:database / resource· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Roberto PresteiD· 3 shared Rosanna ClimaiD· 2 shared Giuseppe GasparreiD· 1 shared Ornella Vitale· 1 shared

Activity by Year

2018-2019 · peak 2/yr

Co-Author Collaboration Network

4 top collaborators · 6 mutual co-author links

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3 shared papersBioinformatics

Roberto PresteORCID

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintSep 17, 2019

Integration of genomic variation and phenotypic data using HmtPhenome

Roberto Preste, Marcella Attimonelli

HmtPhenome integrates genomic variation and phenotypic data to visualize relationships between variants, genes, phenotypes, and diseases related to mitochondrial function.

1 citation

GWAS summary statisticselectronic health records

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BioinformaticsbioRxivPreprintApr 10, 2019

Human mitochondrial variant annotation with HmtNote

Roberto Preste, Rosanna Clima, Marcella Attimonelli

HmtNote annotates human mitochondrial variants from VCF files using data from HmtVar and allows offline use with a local database.

8 citations

humanwhole-genome sequencing

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BioinformaticsNucleic Acids ResearchPeer-reviewedOct 18, 2018

HmtVar: a brand-new resource for human mitochondrial variations and pathogenicity data

Roberto Preste, Ornella Vitale, Rosanna Clima…·Marcella Attimonelli

HmtVar is a database of over 30,000 human mitochondrial variants with pathogenicity predictions, integrating data from HmtDB and third-party annotations.

80 citationstop 3%

humanDNA methylation

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