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TIGAR: transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference.

, , , and . Bioinform., 29 (18): 2292-2299 (2013)

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Estimating copy numbers of alleles from population-scale high-throughput sequencing data., , , , , , and . BMC Bioinform., 16 (S-1): S4 (2015)TIGAR: transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference., , , and . Bioinform., 29 (18): 2292-2299 (2013)Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data., , , , , and . BMC Bioinform., 18 (1): 207:1-207:6 (2017)SVEM: A Structural Variant Estimation Method Using Multi-mapped Reads on Breakpoints., , , , , , , , and . AlCoB, volume 8542 of Lecture Notes in Computer Science, page 208-219. Springer, (2014)Estimating Gene Networks from Expression Data and Binding Location Data via Boolean Networks., , , , , and . ICCSA (3), volume 3482 of Lecture Notes in Computer Science, page 349-356. Springer, (2005)HapMonster: A Statistically Unified Approach for Variant Calling and Haplotyping Based on Phase-Informative Reads., , , , , , and . AlCoB, volume 8542 of Lecture Notes in Computer Science, page 107-118. Springer, (2014)A crowdsourced set of curated structural variants for the human genome., , , , , , , , , and 14 other author(s). PLoS Comput. Biol., (2020)Using Protein-Protein Interactions for Refining Gene Networks Estimated from Microarray Data by Bayesian Networks., , , and . Pacific Symposium on Biocomputing, page 336-347. World Scientific, (2004)HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data., , , , , , , , and . BMC Genom., 16 (S-2): S7 (2015)A Bayesian approach for estimating allele-specific expression from RNA-Seq data with diploid genomes., , , , and . BMC Genom., 17 (S-1): 2 (2016)