Genome Res.

In the effort to prepare the mouse full-length cDNA encyclopedia, we previously developed several techniques to prepare and select full-length cDNAs. To increase the number of different cDNAs, we introduce here a strategy to prepare normalized and subtracted cDNA libraries in a single step. The method is based on hybridization of the first-strand, full-length cDNA with several RNA drivers, including starting mRNA as the normalizing driver and run-off transcripts from minilibraries containing highly expressed genes, rearrayed clones, and previously sequenced cDNAs as subtracting drivers. Our method keeps the proportion of full-length cDNAs in the subtracted/normalized library high. Moreover, our method dramatically enhances the discovery of new genes as compared to results obtained by using standard, full-length cDNA libraries. This procedure can be extended to the preparation of full-length cDNA encyclopedias from other organisms.

Source:http://purl.uniprot.org/citations/11042159

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http://purl.uniprot.org/cit...rdfs:commentIn the effort to prepare the mouse full-length cDNA encyclopedia, we previously developed several techniques to prepare and select full-length cDNAs. To increase the number of different cDNAs, we introduce here a strategy to prepare normalized and subtracted cDNA libraries in a single step. The method is based on hybridization of the first-strand, full-length cDNA with several RNA drivers, including starting mRNA as the normalizing driver and run-off transcripts from minilibraries containing highly expressed genes, rearrayed clones, and previously sequenced cDNAs as subtracting drivers. Our method keeps the proportion of full-length cDNAs in the subtracted/normalized library high. Moreover, our method dramatically enhances the discovery of new genes as compared to results obtained by using standard, full-length cDNA libraries. This procedure can be extended to the preparation of full-length cDNA encyclopedias from other organisms.lld:uniprot
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http://purl.uniprot.org/cit...uniprot:nameGenome Res.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorMuramatsu M.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorKonno H.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorShibata K.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorShibata Y.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorSugahara Y.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorItoh M.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorHayashizaki Y.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorOkazaki Y.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorHayatsu N.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorCarninci P.lld:uniprot
http://purl.uniprot.org/cit...uniprot:date2000lld:uniprot
http://purl.uniprot.org/cit...uniprot:pages1617-1630lld:uniprot
http://purl.uniprot.org/cit...uniprot:titleNormalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.lld:uniprot
http://purl.uniprot.org/cit...uniprot:volume10lld:uniprot
http://purl.uniprot.org/cit...dc-term:identifierdoi:10.1101/gr.145100lld:uniprot
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