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Tatiana G. Popova
Person information
- affiliation: Institut Curie, Paris, France
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2020 – today
- 2021
- [j5]Jorge Ulises Muñoz-Minjares
, Yuriy S. Shmaliy, Tatiana G. Popova:
Critical evaluation of CNA estimators for DNA data using matching confidence masks and WGS technology. Biomed. Signal Process. Control. 70: 103004 (2021) - 2020
- [j4]Alexandre Eeckhoutte, Alexandre Houy, Elodie Manié, Manon Reverdy, Ivan Bièche, Elisabetta Marangoni, Oumou Goundiam, Anne Vincent-Salomon, Dominique Stoppa-Lyonnet, François-Clément Bidard, Marc-Henri Stern
, Tatiana G. Popova:
ShallowHRD: detection of homologous recombination deficiency from shallow whole genome sequencing. Bioinform. 36(12): 3888-3889 (2020)
2010 – 2019
- 2019
- [j3]Jorge Muñoz-Minjares
, Yuriy S. Shmaliy, Tatiana G. Popova:
Correcting estimates of DNA CNAs using improved confidence masks tuned to gold standard. IET Signal Process. 13(4): 464-471 (2019) - [c2]Jorge Muñoz-Minjares
, Yuriy S. Shmaliy, Tatiana G. Popova, Janette Perez-Chimal, Jose Lopez-Robles, Misael Lopez-Ramirez:
Comparison between CNA Estimators and WGS technology based on the Refinement of Breakpoints using the Confidence Masks. CCE 2019: 1-6 - 2018
- [c1]Jorge Muñoz-Minjares
, Yuriy S. Shmaliy, Tatiana G. Popova, R. J. Perez-Chimal:
Matching Confidence Masks with Experts Annotations for Estimates of Chromosomal Copy Number Alterations. IWBBIO (2) 2018: 85-94 - 2014
- [j2]Valentina Boeva
, Tatiana G. Popova, Maxime Lienard, Sebastien Toffoli, Maud Kamal, Christophe Le Tourneau, David Gentien, Nicolas Servant
, Pierre Gestraud
, Thomas Rio Frio
, Philippe Hupé
, Emmanuel Barillot
, Jean-François Laes:
Multi-factor data normalization enables the detection of copy number aberrations in amplicon sequencing data. Bioinform. 30(24): 3443-3450 (2014) - 2012
- [j1]Valentina Boeva
, Tatiana G. Popova, Kevin Bleakley, Pierre Chiche, Julie Cappo, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey
, Olivier Delattre
, Emmanuel Barillot
:
Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data. Bioinform. 28(3): 423-425 (2012)
Coauthor Index
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