Table 1.
Library | RPCI-23 | RPCI-24 | Total |
---|---|---|---|
Sequencing success rate (%)a | 83 | 79 | 81 |
Mouse BAC end sequences (mBESs) | 274277 | 174957 | 449234 |
Clones with ≥1 end and coverageb | 154795, 10X | 102524, 5.3X | 257318, 15.3X |
Paired-end clones and coveragec | 119483, 77%, 7.9X | 72433, 71%, 3.7X | 191916, 75%, 11.6X |
Edited read length,d avg. ± S.D. bp | 466 ± 162 | 515 ± 188 | 485 ± 174 |
Total bases, Mb | 128 | 90 | 218 |
Avg. Q20 bases after trimminge, bp | 387 ± 154 | 438 ± 179 | 406 ± 166 |
Repeat contents, %mBES and %basesf | 63 & 36.5 | 66 & 37.5 | 64 & 37 |
Clones with ≥100 unique Q20 basesg | 65% | 66% | 66% |
%mBESs matching mouse ESTs | 2.2 | 4.5 | 3 |
hClone tracking accuracy | >95% | >95% | >95% |
Percent of sequencing attempts that yielded reads with an overall error rate <2.5%, an edited read length >100 bp, and free of E. coli and vector sequences.
Clones with at least one end sequence. Clone coverage was calculated assuming an average insert size of 197 kb for PRCI-23 library and 155kb for PCRI-24 library, and a genome size of 3 Gb.
Clones with both T7 and Sp6 end sequences (pairs). Clone coverage by pairs was calculated as described above. Total number of pairs, % of pairs in the database, and their coverage are shown.
Read length after sequences were trimmed. The average and standard deviation (S.D.) are shown.
Average number of bases with phred QV ≥ 20 per sequence after sequences were trimmed. The average and S.D. are shown.
Percent of mBESs that contained repeats and percent of bases that were repeats, analyzed by RepeatMasker.
Percent of paired-end clones that had at least one end with ≥100 bp contiguous unique Q20 bases.
Percent of mBESs that were associated with the correct clone identifiers.