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15 matching publication(s)

Publication	Journal	Year	Score	Verdict
A comprehensive resource of genomic, epigenomic and transcriptomic sequencing data for the black truffle Tuber melanosporum. ⚑ PMID 25392735	Gigascience	2014	61	61/100 ⚑
RNA-sequence analysis of primary alveolar macrophages after in vitro infection with porcine reproductive and respiratory syndrome virus strains of differing vir ⚑ PMID 24643046	PLoS One	2014	41	41/100 ⚑
A consensus approach to vertebrate de novo transcriptome assembly from RNA-seq data: assembly of the duck (Anas platyrhynchos) transcriptome. PMID 25009556	Front Genet	2014	67	67/100
Bayesian transcriptome assembly. PMID 25367074	Genome Biol	2014	68	L1 68/100
WikiPathways App for Cytoscape: Making biological pathways amenable to network analysis and visualization. PMID 25254103	F1000Res	2014	76	L1 76/100
OptiType: precision HLA typing from next-generation sequencing data. PMID 25143287	Bioinformatics	2014	95	L1 95/100
A comparative study of techniques for differential expression analysis on RNA-Seq data. PMID 25119138	PLoS One	2014	58	L1 58/100
High-resolution mapping of transcriptional dynamics across tissue development reveals a stable mRNA-tRNA interface. PMID 25122613	Genome Res	2014	87	L1 87/100
Nucleosome regulatory dynamics in response to TGFβ. PMID 24771338	Nucleic Acids Res	2014	59	L1 59/100
Enriched domain detector: a program for detection of wide genomic enrichment domains robust against local variations. PMID 24782521	Nucleic Acids Res	2014	79	L1 79/100
LaSSO, a strategy for genome-wide mapping of intronic lariats and branch points using RNA-seq. PMID 24709818	Genome Res	2014	68	L1 68/100
HTSstation: a web application and open-access libraries for high-throughput sequencing data analysis. PMID 24475057	PLoS One	2014	66	L1 66/100
RASopathy-associated CBL germline mutations cause aberrant ubiquitylation and trafficking of EGFR. PMID 25178484	—	2014	—	L1 No computation
A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm. PMID 24193348	European Journal of Human Genetics	2014	83	L1 83/100
Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infant PMID 24529129	—	2014	—	L1 No computation