Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Monica Valecha"'
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
Autor:
Joao M. Alves, Nuria Estévez-Gómez, Monica Valecha, Sonia Prado-López, Laura Tomás, Pilar Alvariño, Roberto Piñeiro, Laura Muinelo-Romay, Patricia Mondelo-Macía, Mercedes Salgado, Agueda Iglesias-Gómez, Laura Codesido-Prada, Joaquin Cubiella, David Posada
The genomic profiling of circulating tumor cells (CTCs) in the bloodstream should provide clinically relevant information on therapeutic efficacy and help predict cancer survival. However, the molecular characterization of CTCs has so far proven extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8799061e3d41987d8eb4acffc65e8d46
https://doi.org/10.1101/2022.06.02.22275905
https://doi.org/10.1101/2022.06.02.22275905
Autor:
Manita Bansal, Venkateshwar B Rao, Satrupa Das, Monica Valecha, Anjana Munshi, Preeti Khetarpal, Rohitashw 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