Author

Irina V. Shcherbakova

Ludwig-Maximilians-Universität München

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alexander V. PredeusiD· 1 shared Andrey Sergeyevich GlotoviD· 1 shared Anna Aleksandrovna KostarevaiD· 1 shared Artem M. KiseleviD· 1 shared Dmitrii E. PoleviD· 1 shared Elena A. SerebryakovaiD· 1 shared Oleg S. GlotoviD· 1 shared Yury A. BarbitoffiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenomics

Alexander V. PredeusORCID

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1 paper

Recent·Most cited

GenomicsScientific ReportsPeer-reviewedFeb 6, 2020

Systematic dissection of biases in whole-exome and whole-genome sequencing reveals major determinants of coding sequence coverage

Yury A. Barbitoff, Dmitrii E. Polev, Andrey Sergeyevich Glotov…·Alexander V. Predeus

This study systematically evaluates coverage biases in whole-exome and whole-genome sequencing, finding that some WES platforms outperform others and that WES can match WGS in variant discovery.

143 citationstop 1%

humanwhole-exome sequencing

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