Tamara S. Simakova

Saint Petersburg, SPE, Russian Federation

Last Updated: 09/26/2026

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Found 9 publications

Distributions of HLA-A, -B, -C, -DRB1 and -DQB1 alleles typed by next generation sequencing in Russian volunteer donors.

Distributions of HLA-A, -B, -C, -DRB1 and -DQB1 alleles typed by next generation sequencing in Russian volunteer donors.

Journal: HLA
Published: August 20, 2022

SARS-CoV-2 escape from cytotoxic T cells during long-term COVID-19.

SARS-CoV-2 escape from cytotoxic T cells during long-term COVID-19.

Journal: Nature communications
Published: October 24, 2021

NovAT tool-Reliable novel HLA alleles identification from next-generation sequencing data.

NovAT tool-Reliable novel HLA alleles identification from next-generation sequencing data.

Journal: HLA
Published: June 23, 2021

Description of four new HLA alleles: HLA-A*01:288, -A*02:06:23, -A*32:121 and -DRB1*07:100.

Description of four new HLA alleles: HLA-A*01:288, -A*02:06:23, -A*32:121 and -DRB1*07:100.

Journal: HLA
Published: February 04, 2019

Identification of the novel HLA-C*02:151 allele in Russian bone marrow donors.

Identification of the novel HLA-C*02:151 allele in Russian bone marrow donors.

Journal: HLA
Published: December 21, 2018

Design and verification of the reagent kit for high-productive HLA-typing of potential donors of hemopoietic stem cells.

Design and verification of the reagent kit for high-productive HLA-typing of potential donors of hemopoietic stem cells.

Journal: Klinicheskaia laboratornaia diagnostika
Published: November 22, 2018

The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.

The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.

Journal: Klinicheskaia laboratornaia diagnostika
Published: November 30, 2016

A statistical approach to detection of copy number variations in PCR-enriched targeted sequencing data.

A statistical approach to detection of copy number variations in PCR-enriched targeted sequencing data.

Journal: BMC bioinformatics
Published: June 01, 2016

Identification of a novel, CF-causing compound genotype (p.S1159P and p.Y569H) using an NGS-based assay: Novel CF-causing compound p.S1159P and p.Y569H genotype.

Identification of a novel, CF-causing compound genotype (p.S1159P and p.Y569H) using an NGS-based assay: Novel CF-causing compound p.S1159P and p.Y569H genotype.

Journal: Gene
Published: February 23, 2015
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Last Updated: 09/26/2026