Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tiberio Sticca"'
Autor:
Thierry Gil, Ligia Craciun, Tugba Akin Telli, Silvia Camera, Chiara Senti, Ahmad Awada, Caroline Vandeputte, Sophia Leduc, Everardo D. Saad, Joseph Kerger, Andrea Pretta, Alain Hendlisz, Martine Piccart-Gebhart, Denis Larsimont, Philippe Aftimos, Amélie Deleporte, Francesco Sclafani, Pieter Demetter, Pashalina Kehagias, Giacomo Bregni, Elena Trevisi, Tiberio Sticca
Publikováno v:
Acta oncologica (Stockholm, Sweden). 59(12)
High-throughput sequencing technologies are increasingly used in research but limited data are available on the feasibility and value of these when routinely adopted in clinical practice.We analyzed all consecutive cancer patients for whom genomic te
Autor:
Stephane Wenric, Christian Herens, Tiberio Sticca, André Gothot, Mauricette Jamar, Sonia El Guendi, Jean-Hubert Caberg, Claire Josse, Yves Beguin, Vincent Bours, Christophe Poulet, Jo Caers, Stéphanie Max
Publikováno v:
Genes, Chromosomes and Cancer. 56:18-27
The genomic profile of multiple myeloma (MM) has prognostic value by dividing patients into a good prognosis hyperdiploid group and a bad prognosis nonhyperdiploid group with a higher incidence of IGH translocations. This classification, however, is
Autor:
Tiberio, Sticca, Jean-Hubert, Caberg, Stephane, Wenric, Christophe, Poulet, Christian, Herens, Mauricette, Jamar, Claire, Josse, Sonia, El Guendi, Stéphanie, Max, Yves, Beguin, André, Gothot, Jo, Caers, Vincent, Bours
Publikováno v:
Genes, chromosomescancer. 56(1)
The genomic profile of multiple myeloma (MM) has prognostic value by dividing patients into a good prognosis hyperdiploid group and a bad prognosis nonhyperdiploid group with a higher incidence of IGH translocations. This classification, however, is
Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample
Autor:
Claire Josse, Tiberio Sticca, Jo Caers, Christian Herens, Stephane Wenric, Vincent Bours, Mauricette Jamar, Jean-Hubert Caberg, Stéphanie Max, André Gothot, Corinne Fasquelle
Publikováno v:
Genetic epidemiology. 41(1)
An increasing number of bioinformatic tools designed to detect CNVs (copy number variants) in tumor samples based on paired exome data where a matched healthy tissue constitutes the reference have been published in the recent years. The idea of using
Autor:
Caroline Vandeputte, Alain Hendlisz, Francesco Sclafani, Godelieve Machiels, Tugba Akin Telli, Amélie Deleruelle, Ligia Craciun, Denis Larsimont, Maelle Anciaux, Amélie Deleporte, Leila Shaza, Giacomo Bregni, Pieter Demetter, Tiberio Sticca, Silvia Camera
Publikováno v:
Web of Science
216 Background: High-throughput technologies have been increasingly used in research. Nevertheless, limited data are available on the feasibility and clinical value of these technologies in routine practice. Methods: All consecutive GI cancer patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746b34a0d51d7bebd9097c7b167533d4
https://publons.com/wos-op/publon/54204213/
https://publons.com/wos-op/publon/54204213/