Evidence map›Paper›PMID 17568001›Full record

ArticleGenome research2007

Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs).

Yijun Ruan, Hong Sain Ooi, Siew Woh Choo, Kuo Ping Chiu, Xiao Dong Zhao, K G Srinivasan, Fei Yao, Chiou Yu Choo, Jun Liu, Pramila Ariyaratne and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Genome research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
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  3. Kleat: cleavage site analysis of transcriptomes.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2015
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  6. Review
  7. Cancer genome-sequencing study design.Nature reviews. Genetics · 2013
    Review
  8. Using chimaeric expression sequence tag as the reference to identify three-dimensional chromosome contacts.DNA research : an international journal for rapid publication of reports on genes and genomes · 2013
    Article
  9. Article
  10. Article
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 1 country.

Yijun RuanGenome Technology and Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore. ruanyj@gis.a-star.edu.sg
Hong Sain Ooi
Siew Woh Choo
Kuo Ping Chiu
Xiao Dong Zhao
K G Srinivasan
Fei Yao
Chiou Yu Choo
Jun Liu
Pramila Ariyaratne
Wilson G W Bin
Vladimir A Kuznetsov
Atif Shahab
Wing-Kin Sung
Guillaume Bourque
Nallasivam Palanisamy
Chia-Lin Wei
Genome Institute of Singapore · SGBioinformatics Institute · SGNational University of Singapore · SG

Funding

Ditag technologies for complete transcriptome annotationR01HG003521 · NHGRI · GENOME INSTITUTE OF SINGAPORE · PI RUAN, YIJUN · 2004 to 2006
$993k
NHGRI NIH HHS 1R01HG003521-01NHGRI NIH HHS R01 HG003521
6 · The paper itself

Abstract

Identification of unconventional functional features such as fusion transcripts is a challenging task in the effort to annotate all functional DNA elements in the human genome. Paired-End diTag (PET) analysis possesses a unique capability to accurately and efficiently characterize the two ends of DNA fragments, which may have either normal or unusual compositions. This unique nature of PET analysis makes it an ideal tool for uncovering unconventional features residing in the human genome. Using the PET approach for comprehensive transcriptome analysis, we were able to identify fusion transcripts derived from genome rearrangements and actively expressed retrotransposed pseudogenes, which would be difficult to capture by other means. Here, we demonstrate this unique capability through the analysis of 865,000 individual transcripts in two types of cancer cells. In addition to the characterization of a large number of differentially expressed alternative 5' and 3' transcript variants and novel transcriptional units, we identified 70 fusion transcript candidates in this study. One was validated as the product of a fusion gene between BCAS4 and BCAS3 resulting from an amplification followed by a translocation event between the two loci, chr20q13 and chr17q23. Through an examination of PETs that mapped to multiple genomic locations, we identified 4055 retrotransposed loci in the human genome, of which at least three were found to be transcriptionally active. The PET mapping strategy presented here promises to be a useful tool in annotating the human genome, especially aberrations in human cancer genomes.

Indexed as

Genome, HumanTranscription, GeneticTranslocation, GeneticCell Line, TumorChromosomes, Human, Pair 17Chromosomes, Human, Pair 20HumansNeoplasm ProteinsNeoplasmsQuantitative Trait LociRetroelementsSequence Analysis, DNABCAS3 protein, humanBCAS4 protein, humanNeoplasm ProteinsRetroelements

Identifiers

PMID17568001
PMCPMC1891342
OpenAlexW2130022567

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.