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Tatiana G. Popova
Publication Activity (10 Years)
Years Active: 2012-2021
Publications (10 Years): 5
Top Topics
Denoising
Copy Number
Confidence Measures
Top Venues
Bioinform.
Biomed. Signal Process. Control.
CCE
IWBBIO (2)
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Publications
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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 (2021)
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) (2020)
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) (2019)
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)
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)
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) (2014)
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) (2012)