Author

Sei Chang

University of California, Los AngelesORCID 0000-0003-4610-1280Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2

Signature Assays, Organisms & Methods

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Approach:benchmark study· 2 Research Focus:benchmarking· 2 Assay:whole-genome sequencing· 2 Approach:statistical model· 1

Frequent Co-Authors

Eleazar EskiniD· 2 shared Russell LittmaniD· 2 shared Serghei ManguliD· 2 shared Aaron Karlsberg· 1 shared Alex ZelikovskyiD· 1 shared Angela Lu· 1 shared Arda SöyleviD· 1 shared Brian L. HilliD· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersBioinformatics

Eleazar EskinORCID

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2 papers

Recent·Most cited

BioinformaticsbioRxivPreprintApr 16, 2020

A comprehensive benchmarking of WGS-based structural variant callers

Varuni Sarwal, Sebastian Niehus, Ram Ayyala…·Serghei Mangul

This study benchmarks WGS-based structural variant callers using a PCR-confirmed gold standard, finding wide performance variation and identifying tools best suited for low and ultra-low pass data.

5 citations

whole-genome sequencingbenchmark study

𝕏 PostBluesky

BioinformaticsGenome biologyPeer-reviewedMar 17, 2020

Benchmarking of computational error-correction methods for next-generation sequencing data

Keith Mitchell, Jaqueline Brito, Igor Mandric…·Serghei Mangul

This study benchmarks error-correction methods for next-generation sequencing data, finding significant variation in performance across datasets with no single method being optimal overall.

55 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky