Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes

Wittler R, Chauve C (2011)
In: BMC Bioinformatics. BMC.

Conference Paper | Published | English

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RECOMB-CG 2011
Conference Date
2011-10-08
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Wittler R, Chauve C. Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes. In: BMC Bioinformatics. BMC; 2011.
Wittler, R., & Chauve, C. (2011). Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes. BMC Bioinformatics.
Wittler, R., and Chauve, C. (2011). “Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes” in BMC Bioinformatics (BMC).
Wittler, R., & Chauve, C., 2011. Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes. In BMC Bioinformatics. BMC.
R. Wittler and C. Chauve, “Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes”, BMC Bioinformatics, BMC, 2011.
Wittler, R., Chauve, C.: Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes. BMC Bioinformatics. BMC (2011).
Wittler, Roland, and Chauve, Cedric. “Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes”. BMC Bioinformatics. BMC, 2011.
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1 Citation in Europe PMC

Data provided by Europe PubMed Central.

An integrative probabilistic model for identification of structural variation in sequencing data.
Sindi SS, Onal S, Peng LC, Wu HT, Raphael BJ., Genome Biol. 13(3), 2012
PMID: 22452995

34 References

Data provided by Europe PubMed Central.

A unified approach for reconstructing ancient gene clusters.
Stoye J, Wittler R., IEEE/ACM Trans Comput Biol Bioinform 6(3), 2009
PMID: 19644167
Minimal conflicting sets for the consecutive ones property in ancestral genome reconstruction.
Chauve C, Hausd UU, Stephen T, You VP., J. Comput. Biol. 17(9), 2010
PMID: 20874402

AUTHOR UNKNOWN, 1978
Loss of constitutional heterozygosity in human cancer.
Lasko D, Cavenee W, Nordenskjold M., Annu. Rev. Genet. 25(), 1991
PMID: 1687498
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.
Lee S, Hormozdiari F, Alkan C, Brudno M., Nat. Methods 6(7), 2009
PMID: 19483690
MoGUL: Detecting Common Insertions and Deletions in a Population
AUTHOR UNKNOWN, 2010
Paired-end mapping reveals extensive structural variation in the human genome.
Korbel JO, Urban AE, Affourtit JP, Godwin B, Grubert F, Simons JF, Kim PM, Palejev D, Carriero NJ, Du L, Taillon BE, Chen Z, Tanzer A, Saunders AC, Chi J, Yang F, Carter NP, Hurles ME, Weissman SM, Harkins TT, Gerstein MB, Egholm M, Snyder M., Science 318(5849), 2007
PMID: 17901297
The European Genome-Phenome Archive
AUTHOR UNKNOWN, 0

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