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BMC Bioinformatics|April 26, 2022
Variance of allele balance calculated from low coverage sequencing data infers departure from a diploid stateKyle Fletcher, Rongkui Han, Diederik Smilde, et al.BMC Bioinformatics|April 28, 2022
Comparison of five supervised feature selection algorithms leading to top features and gene signatures from multi-omics data in cancerTapas Bhadra, Saurav Mallik, Neaj Hasan, et al.BMC Bioinformatics|October 15, 2021
Quantitative prediction model for affinity of drug-target interactions based on molecular vibrations and overall system of ligand-receptorXian-Rui Wang, Ting-Ting Cao, Cong Min Jia, et al.BMC Bioinformatics|October 17, 2021
Reference-agnostic representation and visualization of pan-genomesQihua Liang, Stefano LonardiBMC Bioinformatics|October 17, 2021
Identifying piRNA targets on mRNAs in C. elegans using a deep multi-head attention networkTzu-Hsien Yang, Sheng-Cian Shiue, Kuan-Yu Chen, et al.BMC Bioinformatics|October 16, 2021
Annotation depth confounds direct comparison of gene expression across speciesElias Oziolor, Seda Arat, Matthew MartinBMC Bioinformatics|October 16, 2021
Tailored graphical lasso for data integration in gene network reconstructionCamilla Lingjærde, Tonje G Lien, Ørnulf Borgan, et al.BMC Bioinformatics|October 30, 2021
isoCNV: in silico optimization of copy number variant detection from targeted or exome sequencing dataRosa Barcelona-Cabeza, Walter Sanseverino, Riccardo Aiese CiglianoBMC Bioinformatics|October 31, 2021
Filling gaps of genome scaffolds via probabilistic searching optical maps against assembly graphBin Huang, Guozheng Wei, Bing Wang, et al.BMC Bioinformatics|October 31, 2021
LongStitch: high-quality genome assembly correction and scaffolding using long readsLauren Coombe, Janet X Li, Theodora Lo, et al.Pageof 1,249