Author

Elena A. Serebryakova

Research Institute of Obstetrics and Gynecology named after D.O. OttORCID 0000-0002-7583-3379Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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 Irina V. Shcherbakova· 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

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Alexander V. PredeusORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

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, Elena A. Serebryakova, Irina V. Shcherbakova, Artem M. Kiselev, Anna Aleksandrovna Kostareva, Oleg S. 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.

Scientific Reports · Feb 6, 2020Peer-reviewedGenomics