Figure 3
From: Improving the performance of true single molecule sequencing for ancient DNA

Nucleotide misincorporation patterns observed on extracts CA1 and CA2. The frequencies of all possible mismatches and indels observed between the horse genome and the reads are reported in grey as a function of the position on sequencing reads, except for C→T, G→A, insertions, and deletions that are reported in blue, red, pink, and green respectively. Only the first 25 nucleotides sequenced are considered. Left: CA1 extract. Right: CA2 extract. Template preparation procedures for tSMS sequencing are reported on the left hand side of the graphs. All graphs correspond to the analyses of horse reads (80°C, 95°C, and 80°C + Spiking) except for the ones labelled 80°C olig. that refer to the analysis of reads mapping against the 30 oligonucleotides used for spiking.