To evaluate DNA preservation and potential for obtaining genome-wide data, an initial ‘screening’ sequencing run was performed with all five Gjerrild libraries pooled together. The criteria for selecting candidates for deeper sequencing was inspired by previous guidelines [1], excluding samples with an endogenous human DNA content <0.5% and <10% C-T damage in the 5’ends (see below). Furthermore, library clonality and overall sequencing efficiency was evaluated. Libraries from the three best samples (Gjerrild 1,5 and 8) were selected for deeper sequencing with one library sequenced per lane, and the data were merged to sample level as outlined above.

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