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Briefings in Bioinformatics|July 9, 2011
Conceptual framework and pilot study to benchmark phylogenomic databases based on reference gene treesBrigitte Boeckmann, Marc Robinson-Rechavi, Ioannis Xenarios, et al.Briefings in Bioinformatics|September 10, 2015
Methodologies and experimental platforms for generating and analysing microarray and mass spectrometry-based omics data to support P4 medicinePietro H Guzzi, Giuseppe Agapito, Marianna Milano, et al.Briefings in Bioinformatics|September 12, 2015
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genesSteven N Hart, Kara N Maxwell, Tinu Thomas, et al.Briefings in Bioinformatics|December 16, 2014
Making the difference: integrating structural variation detection toolsKe Lin, Sandra Smit, Guusje Bonnema, et al.Briefings in Bioinformatics|January 18, 2015
Detecting associations of rare variants with common diseases: collapsing or haplotyping?Meng Wang, Shili LinBriefings in Bioinformatics|September 5, 2015
Comparison of haplotype-based statistical tests for disease association with rare and common variantsAnanda S Datta, Swati BiswasBriefings in Bioinformatics|September 6, 2015
Gene set analysis approaches for RNA-seq data: performance evaluation and application guidelineYasir Rahmatallah, Frank Emmert-Streib, Galina GlazkoBriefings in Bioinformatics|August 5, 2015
Normalization of circulating microRNA expression data obtained by quantitative real-time RT-PCRFrancesco Marabita, Paola de Candia, Anna Torri, et al.Briefings in Bioinformatics|October 4, 2015
How computer science can help in understanding the 3D genome architectureYoli Shavit, Ivan Merelli, Luciano Milanesi, et al.Briefings in Bioinformatics|January 8, 2016
Multi-hierarchical profiling: an emerging and quantitative approach to characterizing diverse biological networksYingying Zhang, Zhong Wang, Yongyan WangPageof 555