T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population

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Figure 3.
Figure 3.

Number of reads from unplaced contigs mapping across T2T-CHM13 in bins of 100 kbp. For each chromosome, an ideogram including the bands is shown; centromeres are dark red and thinner. The x-axis corresponds to the position on the chromosome. The y-axis is logarithmic and corresponds to the number of reads. The line above each chromosome shows the number of reads mapping to a 100-kbp window.

This Article

  1. Genome Res. 35: 2377-2388

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