Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mónica Valecha"'
Autor:
Miguel Fonseca, José Manuel Cameselle-Teijeiro, João Alves, João Almeida, Pilar Alvariño, Andrés Pérez-Figueroa, Mónica Valecha, Débora Chantada, David Posada, Sonia Prado-López
Publikováno v:
Investigo. Repositorio Institucional de la Universidade de Vigo
Universidade de Vigo (UVigo)
Universidade de Vigo (UVigo)
Financiado para publicación en acceso aberto: Universidade de Vigo/CISUG Human mitochondria can be genetically distinct within the same individual, a phenomenon known as heteroplasmy. In cancer, this phenomenon seems exacerbated, and most mitochondr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41deebe78825d6fb2f0fe19960f68418
https://linkinghub.elsevier.com/retrieve/pii/S088875432200060X
https://linkinghub.elsevier.com/retrieve/pii/S088875432200060X
Autor:
Senbai Kang, Nico Borgsmüller, Monica Valecha, Jack Kuipers, Joao M. Alves, Sonia Prado-López, Débora Chantada, Niko Beerenwinkel, David Posada, Ewa Szczurek
Publikováno v:
Genome Biology, Vol 23, Iss 1, Pp 1-33 (2022)
Abstract We present SIEVE, a statistical method for the joint inference of somatic variants and cell phylogeny under the finite-sites assumption from single-cell DNA sequencing. SIEVE leverages raw read counts for all nucleotides and corrects the acq
Externí odkaz:
https://doaj.org/article/effa6828cc9d44b49baa18e46c9ce1f7
Autor:
Monica Valecha, David Posada
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 20, Iss , Pp 2978-2985 (2022)
Single-cell sequencing has gained popularity in recent years. Despite its numerous applications, single-cell DNA sequencing data is highly error-prone due to technical biases arising from uneven sequencing coverage, allelic dropout, and amplification
Externí odkaz:
https://doaj.org/article/39b6269b502d4053b6454e9241f11ad7
Autor:
Anjana Munshi, Preeti Khetarpal, Satrupa Das, Venkateshwar Rao, Monica Valecha, Manita Bansal, Roshan Kumar
Publikováno v:
Genes and Diseases, Vol 5, Iss 2, Pp 119-122 (2018)
In the present study we attempted a parent–child trio, whole exome sequencing (WES) approach to study Apert's syndrome. Clinical characteristics of the child were noted down and WES was carried out using Ion Torrent System that revealed the presenc
Externí odkaz:
https://doaj.org/article/85636cf0385e4b65b4ecbe0f6496c8fe