Valeriia Kaptelova1, Maria Logacheva2, Anna Speranskaya3, Denis Omelchenko4, Anna Fedotova5, Anastasia Krinitsina6, Andrey Ayginin7, Kamil Khafizov8, Elena Korneenko9, Andrei Samoilov10
1Central Research Institute of Epidemiology, Moscow, Russia, valeriia.kaptelova@gmail.com
2Skolkovo Institute of Science and Technology, Skolkovo, Russia, maria.log@gmail.com
3Central Research Institute of Epidemiology, Moscow, Russia, hanna.s.939@gmail.com
4Institute of Information Transmission Problems, Moscow, Russia, omdeno@gmail.com
5Skolkovo Institute of Science and Technology, Skolkovo, Russia, mikrobiomsu@list.ru
6Lomonosov Moscow State University, Moscow, Russia, ankrina@gmail.com
7FSBI “Center of Strategic Planning” of the Ministry of Health, Moscow, Russia, ayginin75@gmail.com
8FSBI “Center of Strategic Planning” of the Ministry of Health, Moscow, Russia, kkhafizov@gmail.com
9Central Research Institute of Epidemiology, Moscow, Russia, lennatta@yandex.ru
10Central Research Institute of Epidemiology, Moscow, Russia, andrei.samoilov@gmail.com
Metagenomic analysis using high-throughput sequencing is an intensively developing approach nowadays. One of its problems is the adequate quantification of components in metagenomic samples.