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A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data.
Cancers (Basel). 2021 Dec 14;13(24):6283. doi: 10.3390/cancers13246283.
Cancers (Basel). 2021.
PMID: 34944901
Free PMC article.
High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer.
Bertelsen B, Tuxen IV, Yde CW, Gabrielaite M, Torp MH, Kinalis S, Oestrup O, Rohrberg K, Spangaard I, Santoni-Rugiu E, Wadt K, Mau-Sorensen M, Lassen U, Nielsen FC.
Bertelsen B, et al. Among authors: torp mh.
NPJ Genom Med. 2019 Jun 21;4:13. doi: 10.1038/s41525-019-0087-6. eCollection 2019.
NPJ Genom Med. 2019.
PMID: 31263571
Free PMC article.
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