Author

Farnaz Fouladi

University of North Carolina at CharlotteORCID 0000-0003-4369-8720Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1

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Assay:metagenomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

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Anthony A. FodoriD· 1 shared Jacqueline B. Young· 1 shared

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2021-2021 · peak 1/yr

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1 shared paperBioinformatics

Anthony A. FodorORCID

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1 paper

Recent·Most cited

BioinformaticsbioRxivPreprintJan 29, 2021

HashSeq: A Simple, Scalable, and Conservative De Novo Variant Caller for 16S rRNA Gene Datasets

Farnaz Fouladi, Jacqueline B. Young, Anthony A. Fodor

HashSeq detects single-nucleotide variants in 16S rRNA gene datasets using a fast HashMap-based approach and background error estimation, producing conservative and well-supported variant calls.

DOI 10.1101/2021.01.29.428714

metagenomicsstatistical model

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