Penalized likelihood for sparse contingency tables with an application to full-length cDNA libraries

scientific article

Penalized likelihood for sparse contingency tables with an application to full-length cDNA libraries is …
instance of (P31):
scholarly articleQ13442814

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P8978DBLP publication IDjournals/bmcbi/DahindenPEB07
P6179Dimensions Publication ID1004213111
P356DOI10.1186/1471-2105-8-476
P932PMC publication ID2233645
P698PubMed publication ID18072965
P5875ResearchGate publication ID5775395

P50authorPeter BühlmannQ30544174
P2093author name stringGiovanni Parmigiani
Peter Bühlmann
Corinne Dahinden
Mark C Emerick
P2860cites workGene index analysis of the human genome estimates approximately 120,000 genes.Q52077979
EST comparison indicates 38% of human mRNAs contain possible alternative splice forms.Q52971558
Initial sequencing and analysis of the human genomeQ21045365
Finishing the euchromatic sequence of the human genomeQ22122488
Integrative annotation of 21,037 human genes validated by full-length cDNA clonesQ24805388
The transcriptional landscape of the mammalian genomeQ27861110
The effect of higher order RNA processes on changing patterns of protein domain selection: a developmentally regulated transcriptome of type 1 inositol 1,4,5-trisphosphate receptorsQ31150503
Alternative splicing and genome complexityQ33956410
Splice variation in mouse full-length cDNAs identified by mapping to the mouse genomeQ35787067
Has the yo-yo stopped? An assessment of human protein-coding gene numberQ35790493
Frequent alternative splicing of human genesQ40414677
P275copyright licenseCreative Commons Attribution 2.0 GenericQ19125117
P6216copyright statuscopyrightedQ50423863
P304page(s)476
P577publication date2007-12-11
P1433published inBMC BioinformaticsQ4835939
P1476titlePenalized likelihood for sparse contingency tables with an application to full-length cDNA libraries
P478volume8

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cites work (P2860)
Q37523771Bayesian modeling of temporal dependence in large sparse contingency tables
Q38171419Empirical comparison study of approximate methods for structure selection in binary graphical models.
Q34089210Sparse linear modeling of next-generation mRNA sequencing (RNA-Seq) data for isoform discovery and abundance estimation
Q92591104Statistical Methods and Software for Substance Use and Dependence Genetic Research

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