Author

Vincenza Conteduca

Istituto Scientifico Romagnolo per lo Studio e la Cura dei TumoriORCID 0000-0002-6921-714XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anuradha JayaramiD· 1 shared Daniel WetterskogiD· 1 shared Delila Gasi TandefeltiD· 1 shared Dimitrios KleftogiannisiD· 1 shared Gerhardt AttardiD· 1 shared Marco PuntaiD· 1 shared Shahneen Kaur SandhuiD· 1 shared Stefano LiseiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

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9 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Anuradha JayaramORCID

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1 paper

Recent·Most cited

GenomicsBMC Medical GenomicsPeer-reviewedAug 2, 2019

Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

Dimitrios Kleftogiannis, Marco Punta, Anuradha Jayaram…·Stefano Lise

AmpliSolve improves SNV detection in deep sequencing data by estimating position-specific background noise, achieving good precision and sensitivity even at low VAFs.

9 citations

whole-exome sequencingstatistical model

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