Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2002-5-29
pubmed:abstractText
We describe an efficient high-throughput method for accurate DNA sequencing of entire cDNA clones. Developed as part of our involvement in the Mammalian Gene Collection full-length cDNA sequencing initiative, the method has been used and refined in our laboratory since September 2000. Amenable to large scale projects, we have used the method to generate >7 Mb of accurate sequence from 3695 candidate full-length cDNAs. Sequencing is accomplished through the insertion of Mu transposon into cDNAs, followed by sequencing reactions primed with Mu-specific sequencing primers. Transposon insertion reactions are not performed with individual cDNAs but rather on pools of up to 96 clones. This pooling strategy reduces the number of transposon insertion sequencing libraries that would otherwise be required, reducing the costs and enhancing the efficiency of the transposon library construction procedure. Sequences generated using transposon-specific sequencing primers are assembled to yield the full-length cDNA sequence, with sequence editing and other sequence finishing activities performed as required to resolve sequence ambiguities. Although analysis of the many thousands (22 785) of sequenced Mu transposon insertion events revealed a weak sequence preference for Mu insertion, we observed insertion of the Mu transposon into 1015 of the possible 1024 5mer candidate insertion sites.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-10373596, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-10521335, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-11230166, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-11282977, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-12034835, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-1847513, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-2838135, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-6269069, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9063643, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9149950, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9224593, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9371743, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9521921, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9521922, http://linkedlifedata.com/resource/pubmed/commentcorrection/12034834-9521923
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1362-4962
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2460-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
An efficient strategy for large-scale high-throughput transposon-mediated sequencing of cDNA clones.
pubmed:affiliation
Genome Sciences Centre, BC Cancer Agency, 600 West 10th Avenue, Vancouver, BC V5Z 4E6, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't