Author

Inka Saarinen

Blueprint Genetics (Finland)ORCID 0000-0001-8079-379XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Approach:machine learning (classical)· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jussi PaananeniD· 1 shared Kaloyan Marinov· 1 shared Leo LahtiiD· 1 shared Mikko SärkkäiD· 1 shared Sami Myöhänen· 1 shared Vittorio FortinoiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperBioinformatics

Jussi PaananenORCID

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1 paper

Recent·Most cited

BioinformaticsbioRxivPreprintJun 17, 2022

Comparison of missing data handling methods for variant pathogenicity predictors

Mikko Särkkä, Sami Myöhänen, Kaloyan Marinov…·Jussi Paananen

The paper compares missing data handling methods for variant pathogenicity predictors and finds that simpler imputation methods like mean imputation perform best.

2 citations

whole-exome sequencingwhole-genome sequencing

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