Author

Renato Salazar

Johannes Kepler University of LinzORCID 0000-0001-8436-9304Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:variant calling· 4 Approach:experimental assay· 3 Approach:statistical model· 3 Organism:human· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:software / tool· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Irene Tiemann‐BoegeiD· 4 shared Monika HeinzliD· 4 shared Anton NekrutenkoiD· 2 shared Barbara ArbeithuberiD· 2 shared Gundula PovysiliD· 2 shared Nicholas StoleriD· 2 shared Theresa MairiD· 2 shared Angelika LahnsteineriD· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Irene Tiemann‐BoegeORCID

Mutual co-authors in cluster

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4 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Breast CancerPeer-reviewedJun 29, 2022

High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing.

Anna Kostecka, Tomasz Nowikiewicz, Paweł Olszewski…·Arkadiusz Piotrowski

27 citations

humanwhole-exome sequencing

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GeneticsGenome ResearchPeer-reviewedMar 1, 2022

Discovery of an unusual high number of de novo mutations in sperm of older men using duplex sequencing

Renato Salazar, Barbara Arbeithuber, Maja Ivankovic…·Irene Tiemann‐Boege

The paper uses duplex sequencing to analyze de novo mutations in sperm DNA from older and younger donors, finding higher mutation frequencies and recurrence in older donors.

24 citations

humanwhole-exome sequencing

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GenomicsNAR Genomics and BioinformaticsPeer-reviewedJan 6, 2021

Increased yields of duplex sequencing data by a series of quality control tools

Gundula Povysil, Monika Heinzl, Renato Salazar…·Irene Tiemann‐Boege

The paper develops quality control tools to improve duplex sequencing data yields by reducing data loss and enhancing variant calling accuracy.

8 citations

whole-genome sequencingstatistical model

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BioinformaticsBMC BioinformaticsPeer-reviewedMar 4, 2020

Family reunion via error correction: An efficient analysis of duplex sequencing data

Nicholas Stoler, Barbara Arbeithuber, Gundula Povysil…·Anton Nekrutenko

The paper corrects errors in duplex sequencing data to reunite reads and improve the efficiency of variant detection.

13 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky