Figure 1.
Physical coverage for each library. The fraction of the non-gap positions covered by zero, one, two to three, and four or more concordant clones is shown for the autosomes (A) and chromosome X (B). The fraction is calculated based on the location of fosmid end-sequence pairs that mapped to a “best” location in the human genome (build36). All libraries were derived from female cell lines with the exception of ABC8 (NA18507).
