Código QR (código de barras bidimensional)

Leveraging sequences missing from the human genome to diagnose cancer

Abstract Background Cancer diagnosis using cell-free DNA (cfDNA) has the potential to improve treatment and survival but has several technical limitations. Methods In this study, we developed a prediction model based on neomers, DNA sequences 13–17 nucleotides in length that are predominantly absent...

ver descrição completa

Na minha lista:
Principais autores: Ilias Georgakopoulos-Soares, Ofer Yizhar-Barnea, Ioannis Mouratidis, Candace S. Y. Chan, Michail Patsakis, Akshatha Nayak, Rachael Bradley, Mayank Mahajan, Jasmine Sims, Dianne Laboy Cintron, Ryder Easterlin, Julia S. Kim, Emmalyn Chen, Geovanni Pineda, Guillermo E. Parada, John S. Witte, Christopher A. Maher, Felix Feng, Ioannis Vathiotis, Nikolaos Syrigos, Emmanouil Panagiotou, Andriani Charpidou, Konstantinos Syrigos, Jocelyn Chapman, Mark Kvale, Martin Hemberg, Nadav Ahituv
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Portfolio 2025-08-01
coleção:Communications Medicine
Acesso em linha:https://doi.org/10.1038/s43856-025-01067-3
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados