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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Biotechnology and Bi...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Biotechnology and Bioengineering
Article . 2010 . Peer-reviewed
License: Wiley Online Library User Agreement
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Reaching the depth of the Chinese hamster ovary cell transcriptome

Authors: Nitya M, Jacob; Anne, Kantardjieff; Faraaz Noor Khan, Yusufi; Ernest F, Retzel; Bhanu Chandra, Mulukutla; Song Hui, Chuah; Miranda, Yap; +1 Authors

Reaching the depth of the Chinese hamster ovary cell transcriptome

Abstract

AbstractThe high‐throughput DNA sequencing Illumina Solexa GAII platform was employed to characterize the transcriptome of an antibody‐producing Chinese hamster ovary (CHO) cell line. More than 55 million sequencing reads were generated and mapped to an existing set of CHO unigenes derived from expressed sequence tags (ESTs), as well as several public sequence databases. A very significant fraction of sequencing reads has not been previously seen. The frequency with which fragments of a unigene were sequenced was taken as an estimate of the abundance level of the corresponding transcripts. A wide dynamic range of transcript abundance levels was observed, spanning six orders of magnitude. However, the distribution of coverage across transcript lengths was found to vary, from relatively uniform to highly variable. This observation suggests that more challenges are yet to be resolved before direct sequencing can be used as a true quantitative measure of transcript level and for differential gene expression analysis. With the depth that high‐throughput sequencing methods can reach, one can expect that the entire transcriptome of this industrially important organism will be decoded in the near future. Biotechnol. Bioeng. 2010;105: 1002–1009. © 2009 Wiley Periodicals, Inc.

Keywords

Expressed Sequence Tags, Gene Expression Profiling, CHO Cells, Sequence Analysis, DNA, Antibodies, Recombinant Proteins, Cricetulus, Cricetinae, Animals, Female, RNA, Messenger

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
29
Average
Top 10%
Top 10%
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