Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jorge Francisco Cutigi"'
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Identifying significantly mutated genes in cancer is essential for understanding the mechanisms of tumor initiation and progression. This task is a key challenge since large-scale genomic studies have reported an endless number of genes muta
Externí odkaz:
https://doaj.org/article/2e76dee92a5d42cab49b80c1f6072f83
Autor:
Jorge Francisco Cutigi
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
O teste baseado em modelos visa à derivação de casos de teste a partir de modelos produzidos ao longo do desenvolvimento de software. Nesse contexto, as Máquinas de Estados Finitos têm sido amplamente pesquisadas e utilizadas para derivação de
Autor:
Paulo Henrique Ribeiro, Jorge Francisco Cutigi, Adriane Feijó Evangelista, Adenilso da Silva Simão
Publikováno v:
Anais do XXII Simpósio Brasileiro de Computação Aplicada à Saúde (SBCAS 2022).
As células com mutações drivers podem proliferar mais rapidamente do que outras células, gerando mais células-filhas e ocasionando o surgimento do tumor. Nesse contexto, existem métodos computacionais para identificar possíveis mutações driv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939707d39562ef8f8992ef1d0f5efb73
https://doi.org/10.5753/sbcas.2022.222451
https://doi.org/10.5753/sbcas.2022.222451
Publikováno v:
Anais Estendidos do XXII Simpósio Brasileiro de Computação Aplicada à Saúde (SBCAS 2022).
O câncer é uma doença complexa provocada por alterações genéticas que se acumulam por toda a vida do indivíduo. A essas alterações dá-se o nome de mutação genética. Células de câncer possuem um elevado número de mutações, das quais
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c806e680cfc7388619a839659acfa39
https://doi.org/10.5753/sbcas_estendido.2022.222427
https://doi.org/10.5753/sbcas_estendido.2022.222427
Autor:
Jorge Francisco Cutigi
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Cancer is a complex disease caused by the accumulation of genetic alterations during the individuals life. These alterations are named genetic mutations, which may be divided into two groups: 1) Passenger mutations: mutations that do not change the b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c49de42912bf035584a285d2bc0b720
https://doi.org/10.11606/t.55.2021.tde-18082021-100555
https://doi.org/10.11606/t.55.2021.tde-18082021-100555
Autor:
Adenilso Simao, Rodrigo Henrique Ramos, Jorge Francisco Cutigi, Cynthia de Oliveira Lage Ferreira
Publikováno v:
Advances in Bioinformatics and Computational Biology ISBN: 9783030918132
Cancer is a complex disease caused by genetic mutations categorized into two groups: passenger and driver. Contrary to passenger, drivers mutations directly impact oncogenesis. Drivers identification is a challenge in cancer genomics, frequently supp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebf2aacc3abc33d93bb3d699e0f1565f
https://doi.org/10.1007/978-3-030-91814-9_3
https://doi.org/10.1007/978-3-030-91814-9_3
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Cancer is a complex disease caused by the accumulation of genetic alterations during the individual’s life. Such alterations are called genetic mutations and can be divided into two groups: (1) Passenger mutations, which are not responsible for can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63fff9e48fc2103bba72426cd916f4f9
https://pubmed.ncbi.nlm.nih.gov/32698724
https://pubmed.ncbi.nlm.nih.gov/32698724
Autor:
Cynthia de Oliveira Lage Ferreira, Renato Feijo Evangelista, Adriane Feijó Evangelista, André C. P. L. F. de Carvalho, Rodrigo Henrique Ramos, Jorge Francisco Cutigi, Adenilso Simao
Publikováno v:
Advances in Bioinformatics and Computational Biology ISBN: 9783030657741
BSB
BSB
An increasing interest in Cancer Genomics research emerged from the advent and widespread use of next-generation sequencing technologies, which have generated a large amount of digital biological data. However, not all of this information in fact con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df7280e97dc8a750a6086dedd60bd4b8
https://doi.org/10.1007/978-3-030-65775-8_8
https://doi.org/10.1007/978-3-030-65775-8_8
Publikováno v:
Advances in Bioinformatics and Computational Biology ISBN: 9783030464165
BSB
BSB
Identifying significant mutations in cancer is a challenging problem in Cancer Genomics. Computational methods for identifying significant mutations have been developed in recent years. In this work, we present a flexible computational method named G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5536147fc2cb83f69fd0d1cea6d6c94d
https://doi.org/10.1007/978-3-030-46417-2_3
https://doi.org/10.1007/978-3-030-46417-2_3
Publikováno v:
Anais do Simpósio Brasileiro de Computação Aplicada à Saúde (SBCAS 2019).
Identifying significant mutations in cancer is a key point in Cancer Genomics, and it is one of the biggest challenges in the area. Computational methods for identifying significant mutations have been developed in recent years. In this work, we pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50f7fa6be4109317eb57f2a486ffe29c
https://doi.org/10.5753/sbcas.2019.6266
https://doi.org/10.5753/sbcas.2019.6266