I. Stetsenko

发表

Effect of DNA insert length on whole-exome sequencing enrichment efficiency: an observational study

A. Krasnenko, V. Ilinsky, Kirill Tsukanov, 2018 .

Breast cancer: analysis of driver somatic mutations detected by next-generation sequencing

S. A. Zarubina, D. Korostin, V. V. Il’inskii, 2017 .

Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers

A. Rakitko, E. Nikolaeva, A. Krasnenko, 2020, Molecular genetics & genomic medicine.

Genomic Variability of SARS-CoV-2 Omicron Variant Circulating in the Russian Federation during Early December 2021 and Late January 2022

E. Chernyaeva, G. Shipulin, A. Ayginin, 2022, Pathogens.

Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report

E. Il’ina, A. Krasnenko, V. Ilinsky, 2020, BMC medical genetics.

Development and application of an RT‒PCR assay for the identification of the delta and omicron variants of SARS-COV-2

K. B. Kolbutova, G. Shipulin, I. Stetsenko, 2023, Heliyon.

SARS-CoV-2 Recombination and Coinfection Events Identified in Clinical Samples in Russia

E. Chernyaeva, G. Shipulin, I. Stetsenko, 2023, Viruses.

Ultra-Low Coverage Sequencing as the Most Accurate Library Quantification Method Prior to Target Sequencing

A. Rakitko, V. Demkin, I. Stetsenko, 2019, Molecular Genetics, Microbiology and Virology.

The impact of sequencing depth on accuracy of single nucleotide variant calls

V. Ilinsky, D. Plakhina, I. Stetsenko, 2017 .