| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/jcb/FengLJ11 |
| P356 | DOI | 10.1089/CMB.2010.0243 |
| P932 | PMC publication ID | 3123862 |
| P698 | PubMed publication ID | 21385036 |
| P5875 | ResearchGate publication ID | 50347201 |
| P2093 | author name string | Wei Li | |
| Jianxing Feng | |||
| Tao Jiang | |||
| P2860 | cites work | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | Q21061203 |
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| The connection between splicing and cancer. | Q36513592 | ||
| The turning point in genome research | Q36693819 | ||
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| P433 | issue | 3 | |
| P1104 | number of pages | 17 | |
| P304 | page(s) | 305-321 | |
| P577 | publication date | 2011-03-01 | |
| P1433 | published in | Journal of Computational Biology | Q6295003 |
| P1476 | title | Inference of isoforms from short sequence reads | |
| P478 | volume | 18 |
| Q39850400 | A Network of Splice Isoforms for the Mouse |
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| Q37172278 | Cardiovascular transcriptomics and epigenomics using next-generation sequencing: challenges, progress, and opportunities |
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| Q35970681 | Deciphering the plant splicing code: experimental and computational approaches for predicting alternative splicing and splicing regulatory elements |
| Q37194744 | Functional Networks of Highest-Connected Splice Isoforms: From The Chromosome 17 Human Proteome Project. |
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| Q36740961 | Modeling RNA degradation for RNA-Seq with applications |
| Q30690326 | Modeling alternative splicing variants from RNA-Seq data with isoform graphs |
| Q33565443 | Next-generation sequencing: from understanding biology to personalized medicine |
| Q34121449 | Overview of available methods for diverse RNA-Seq data analyses |
| Q30870540 | RNA-Seq Data: A Complexity Journey |
| Q34018852 | RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders |
| Q29547458 | RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome |
| Q61446149 | Reconstruction of full-length circular RNAs enables isoform-level quantification |
| Q31121567 | SDEAP: a splice graph based differential transcript expression analysis tool for population data |
| Q34463372 | StringTie enables improved reconstruction of a transcriptome from RNA-seq reads |
| Q21145302 | Systematically differentiating functions for alternatively spliced isoforms through integrating RNA-seq data |
| Q28728363 | The human transcriptome: an unfinished story |
| Q58765268 | TraRECo: a greedy approach based de novo transcriptome assembler with read error correction using consensus matrix |
| Q37349453 | TransComb: genome-guided transcriptome assembly via combing junctions in splicing graphs |
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| Q30579842 | iReckon: simultaneous isoform discovery and abundance estimation from RNA-seq data |
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