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Published Erratum
. 2021 Aug;32(8):1069-1071.
doi: 10.1016/j.annonc.2021.05.798. Epub 2021 Jun 2.

Erratum to 'Germline-focussed analysis of tumour-only sequencing: recommendations from the ESMO Precision Medicine Working Group': [Annals of Oncology 30 (2019) 1221-1231]

Affiliations
Published Erratum

Erratum to 'Germline-focussed analysis of tumour-only sequencing: recommendations from the ESMO Precision Medicine Working Group': [Annals of Oncology 30 (2019) 1221-1231]

D Mandelker et al. Ann Oncol. 2021 Aug.
No abstract available

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Figures

Figure 1
Figure 1
Distribution of variant allele frequency observed in the tumour for variants of true germline origin which were (i) small insertion/deletions (ii) SNVs.
Figure 2
Figure 2
Distribution of germline and somatic pathogenic variants detected upon tumour analysis. Only variants classified pathogenic/likely pathogenic AND above VAF threshold are included (blue, germline origin; red, somatic origin; numbers, total number of pathogenic variants. observed in tumour).
Figure 3
Figure 3
Distribution of germline and somatic pathogenic variants detected upon tumour analysis for 30 high-actionability CSGs. (A) Offtumour and (B) on-tumour.

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