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BMC Bioinformatics|March 6, 2022
CNVind: an open source cloud-based pipeline for rare CNVs detection in whole exome sequencing data based on the depth of coverageWiktor Kuśmirek, Robert NowakBMC Bioinformatics|February 26, 2022
DeepWalk based method to predict lncRNA-miRNA associations via lncRNA-miRNA-disease-protein-drug graphLong Yang, Li-Ping Li, Hai-Cheng YiBMC Bioinformatics|March 29, 2022
BarWare: efficient software tools for barcoded single-cell genomicsElliott Swanson, Julian Reading, Lucas T Graybuck, et al.BMC Bioinformatics|April 1, 2022
LANDMark: an ensemble approach to the supervised selection of biomarkers in high-throughput sequencing dataJosip Rudar, Teresita M Porter, Michael Wright, et al.BMC Bioinformatics|April 1, 2022
classifieR a flexible interactive cloud-application for functional annotation of cancer transcriptomesGerard P Quinn, Tamas Sessler, Baharak Ahmaderaghi, et al.BMC Bioinformatics|April 1, 2022
LPMX: a pure rootless composable container systemXu Yang, Masahiro KasaharaBMC Bioinformatics|September 23, 2021
Deep GONet: self-explainable deep neural network based on Gene Ontology for phenotype prediction from gene expression dataVictoria Bourgeais, Farida Zehraoui, Mohamed Ben Hamdoune, et al.BMC Bioinformatics|September 23, 2021
Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusionFrancisco Carrillo-Perez, Juan Carlos Morales, Daniel Castillo-Secilla, et al.BMC Bioinformatics|October 14, 2018
Predicting variant deleteriousness in non-human species: applying the CADD approach in mouseChristian Groß, Dick de Ridder, Marcel ReindersBMC Bioinformatics|October 14, 2018
Finding the mean in a partition distributionThomas J Glassen, Timo von Oertzen, Dmitry A KonovalovPageof 1,248