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. 2010 May 7;5(5):e10517. doi: 10.1371/journal.pone.0010517

Table 2. Assembly statistics and accuracy evaluation for human full-length cDNA clones.

Library 1 Library 1+2
Reference full-length cDNA clones (A) 199 199
Reference clones amplified by PCR (B) 158 158
% (B/A) 79.4% 79.4%
Clones with CDS annotation (C) 141 139
% (C/B) 89.2% 88.0%
Clones with consistent CDS structure (D) 134 135
% (D/C) 95.0% 97.1%
Clones with inconsistent CDS structure (E) 7 4
% (E/C) 5.0% 2.9%

A: The number of the reference full-length cDNA clones used in the experiment. the original number was 200, but one of them was excluded due to chimerism; B: the number of reference full-length cDNA clones successfully amplified by PCR. Note that it does not include non-reference full-length cDNA clones; C: the number of successfully amplified reference full-length cDNA clones with CDS annotation. Non-reference and/or non-amplified full-length cDNA clones were excluded; D: the number of full-length cDNA clones that were reconstructed consistently in terms of CDS structure. See Fig. 2 for CDS structure consistency; E: the number of full-length cDNA clones that were not reconstructed consistently with regard to CDS structure. This always equals to C–D.