High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer

por Bertelsen, Birgitte, Tuxen, Ida Viller, Yde, Christina Westmose, Gabrielaite, Migle, Torp, Mathias Husted, Kinalis, Savvas, Oestrup, Olga, Rohrberg, Kristoffer, Spangaard, Iben, Santoni-Rugiu, Eric, Wadt, Karin, Mau-Sorensen, Morten, Lassen, Ulrik, Nielsen, Finn Cilius
Publicado 2019

A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data

por Gabrielaite, Migle, Torp, Mathias Husted, Rasmussen, Malthe Sebro, Andreu-Sánchez, Sergio, Vieira, Filipe Garrett, Pedersen, Christina Bligaard, Kinalis, Savvas, Madsen, Majbritt Busk, Kodama, Miyako, Demircan, Gül Sude, Simonyan, Arman, Yde, Christina Westmose, Olsen, Lars Rønn, Marvig, Rasmus L., Østrup, Olga, Rossing, Maria, Nielsen, Finn Cilius, Winther, Ole, Bagger, Frederik Otzen
Publicado 2021