Sequencing multimegabase-template DNA with BigDye terminator chemistry
被引:133
作者:
Heiner, CR
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机构:PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
Heiner, CR
Hunkapiller, KL
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机构:PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
Hunkapiller, KL
Chen, SM
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机构:PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
Chen, SM
Glass, JI
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机构:PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
Glass, JI
Chen, EY
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机构:
PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USAPE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
Chen, EY
[1
]
机构:
[1] PE Appl Biosyst, Adv Ctr Genet Technol, Foster City, CA 94404 USA
[2] PE Appl Biosyst, Genet Anal Dept, Foster City, CA 94404 USA
[3] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
来源:
GENOME RESEARCH
|
1998年
/
8卷
/
05期
关键词:
D O I:
10.1101/gr.8.5.557
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Using the recently introduced BigDye(TM) terminators, large-template DNA can be directly sequenced with custom primers on automated instruments. Cycle sequencing conditions are presented to sequence DNA samples isolated From a number of microbial genomes including 750-kb Ureaplasma urealyticum, 1.2-Mb Mycoplasma fermentans, 2.3-Mb Streptococcus pneumoniae, and 4.6-Mb Escherichia coli. Average read lengths of >700 bp from unique primer annealing sites are often sufficient to fill final gaps in microbial genome sequencing projects without additional manipulations of template DNA. The technique can also be applied to sequence-targeted regions, thereby bypassing tedious subcloning steps.