Author

Zachary A. Szpiech

Primary ORCID profile (0000-0001-6372-8224 · 20 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Zachary A. SzpiechiD20 papers · Pennsylvania State University

Biology Disciplines

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Bioinformatics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Behalf of the CAAPA consortium· 1 shared Carlos D. Bustamante· 1 shared Francisco M. De La Vega· 1 shared Kathleen C. Barnes· 1 shared Margaret A. Taub· 1 shared Rasika A. Mathias· 1 shared Raul Torres· 1 shared Ryan D. Hernandez· 1 shared

Activity by Year

2016-2016 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperBioinformatics

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1 paper

Recent·Most cited

BioinformaticsbioRxivPreprintSep 30, 2016

Comparing multi- and single-sample variant calls to improve variant call sets from deep coverage whole-genome sequencing data

Suyash S. Shringarpure, Rasika A. Mathias, Ryan D. Hernandez…·Behalf of the CAAPA consortium

The paper improves variant call sets from deep coverage whole-genome sequencing data by comparing multi- and single-sample variant calls using a Random Forest classifier trained on genotype array data.

DOI 10.1101/078642

humanwhole-genome sequencing

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