Author

Emmanuel Sapin

University of Colorado BoulderORCID 0000-0002-7188-3715Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 3 Organism:human· 2

Frequent Co-Authors

Matthew C. KelleriD· 3 shared Kristen M. KellyiD· 2 shared

Activity by Year

2021-2026 · peak 2/yr

Co-Author Collaboration Network

2 top collaborators · 1 mutual co-author link

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3 shared papersBioinformatics

Matthew C. KellerORCID

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintAug 12, 2026

Near perfect identification of half sibling versus niece/nephew avuncular pairs without pedigree information or genotyped relatives

Emmanuel Sapin, Kristen M. Kelly, Matthew C. Keller

The paper presents a method to distinguish half-sibling from niece/nephew-avuncular pairs using genotype data alone, achieving over 98% accuracy without pedigree information.

DOI 10.64898/2026.01.06.697070

whole-genome sequencingstatistical model

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GenomicsBioinformaticsPeer-reviewedMay 1, 2026

A Novel Method for Across-Chromosome Phasing without Relative Data

Emmanuel Sapin, Kristen M. Kelly, Matthew C. Keller

This paper introduces a novel method for across-chromosome phasing without requiring relative data, achieving high accuracy when within-chromosome phasing is accurate.

DOI 10.1093/bioinformatics/btag277

humanwhole-genome sequencing

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BioinformaticsBioinformaticsPeer-reviewedMar 9, 2021

Novel Approach for Parallelizing Pairwise Comparison Problems as Applied to Detecting Segments Identical By Decent in Whole-Genome Data

Emmanuel Sapin, Matthew C. Keller

The paper introduces a parallelized algorithm for pairwise comparison problems, demonstrating significant efficiency gains in detecting identical by descent segments in whole-genome data.

9 citations

humanwhole-genome sequencing

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