Author

Pantelis Constantoulakis

ORCID 0000-0001-6121-6364Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adrian Willig· 1 shared Aitor Rodríguez‐CasanovaiD· 1 shared Alexandra Saitta· 1 shared Alexandre HarléiD· 1 shared Alexis RapiniD· 1 shared Ali Si-Mohammed· 1 shared Ana Claudia MarquesiD· 1 shared Anes Hadjadj AouliD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenomics

Adrian Willig

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2 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Molecular DiagnosticsPeer-reviewedSep 25, 2025

Analytical Validation of a Pan-Cancer NGS Assay for In-House Liquid Biopsy Testing: An International Multicenter Study

Gaëlle Lescuyer, Alexandre Harlé, Hari Shankar Kumar…·Lea Francoise Payen

This study validates a pan-cancer NGS assay for liquid biopsy testing across multiple centers, showing high sensitivity and specificity for detecting genomic alterations in cfDNA.

3 citations

humanwhole-exome sequencing

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GenomicsClinical Microbiology and InfectionPeer-reviewedApr 2, 2021

Guidelines for accurate genotyping of SARS-CoV-2 using amplicon-based sequencing of clinical samples

Slawomir Kubik, Ana Claudia Marques, Xiaobin Xing…·Zhenyu Xu

This study provides guidelines for accurate SARS-CoV-2 genotyping using amplicon-based sequencing, showing that at least 1000 viral genomes are needed to reliably detect variants at 10% frequency.

37 citations

experimental assay

𝕏 PostBluesky