scholarly article | Q13442814 |
P8978 | DBLP publication ID | journals/bmcbi/DahindenPEB07 |
P6179 | Dimensions Publication ID | 1004213111 |
P356 | DOI | 10.1186/1471-2105-8-476 |
P932 | PMC publication ID | 2233645 |
P698 | PubMed publication ID | 18072965 |
P5875 | ResearchGate publication ID | 5775395 |
P50 | author | Peter Bühlmann | Q30544174 |
P2093 | author name string | Giovanni Parmigiani | |
Peter Bühlmann | |||
Corinne Dahinden | |||
Mark C Emerick | |||
P2860 | cites work | Gene 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 genome | Q21045365 | ||
Finishing the euchromatic sequence of the human genome | Q22122488 | ||
Integrative annotation of 21,037 human genes validated by full-length cDNA clones | Q24805388 | ||
The transcriptional landscape of the mammalian genome | Q27861110 | ||
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 receptors | Q31150503 | ||
Alternative splicing and genome complexity | Q33956410 | ||
Splice variation in mouse full-length cDNAs identified by mapping to the mouse genome | Q35787067 | ||
Has the yo-yo stopped? An assessment of human protein-coding gene number | Q35790493 | ||
Frequent alternative splicing of human genes | Q40414677 | ||
P275 | copyright license | Creative Commons Attribution 2.0 Generic | Q19125117 |
P6216 | copyright status | copyrighted | Q50423863 |
P304 | page(s) | 476 | |
P577 | publication date | 2007-12-11 | |
P1433 | published in | BMC Bioinformatics | Q4835939 |
P1476 | title | Penalized likelihood for sparse contingency tables with an application to full-length cDNA libraries | |
P478 | volume | 8 |
Q37523771 | Bayesian modeling of temporal dependence in large sparse contingency tables |
Q38171419 | Empirical comparison study of approximate methods for structure selection in binary graphical models. |
Q34089210 | Sparse linear modeling of next-generation mRNA sequencing (RNA-Seq) data for isoform discovery and abundance estimation |
Q92591104 | Statistical Methods and Software for Substance Use and Dependence Genetic Research |
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