Bioinformatics
Showing page 64 of 130 pages of list content
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Benchmark of lncRNA Quantification for RNA-Seq of Cancer Samples
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Empowering the annotation and discovery of structured RNAs with scalable and accessible integrative clustering
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DENTIST – using long reads for closing assembly gaps at high accuracy
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Sim3C: simulation of HiC and Meta3C proximity ligation sequencing technologies
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Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
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Genetic demultiplexing of pooled single-cell RNA-sequencing samples in cancer facilitates effective experimental design
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Bias invariant RNA-seq metadata annotation
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Distinguish virulent and temperate phage-derived sequences in metavirome data with a deep learning approach
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FASTQuick: Rapid and comprehensive quality assessment of raw sequence reads
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CAMITAX: Taxon labels for microbial genomes
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