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. 2001 Oct;11(10):1736–1745. doi: 10.1101/gr.179201

Table 1.

TIGR Mouse BAC End Sequencing Efforts (June 27, 2001)

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%
a

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. 

b

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. 

c

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. 

d

Read length after sequences were trimmed. The average and standard deviation (S.D.) are shown. 

e

Average number of bases with phred QV ≥ 20 per sequence after sequences were trimmed. The average and S.D. are shown. 

f

Percent of mBESs that contained repeats and percent of bases that were repeats, analyzed by RepeatMasker

g

Percent of paired-end clones that had at least one end with ≥100 bp contiguous unique Q20 bases. 

h

Percent of mBESs that were associated with the correct clone identifiers.