Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic. #SomaticVariants #ShortReads #LongReads #VariantCalling #Genomics #Bioinformatics #ToolsBenchmarking #ReferenceDatasets @natbiotech.nature.com 🧬 🖥️
www.nature.com/articles/s41...

A comparison of long-read single-cell transcriptomic approaches. #LongRead #Sequencing #SingleCell #Transcriptomics #ToolsBenchmarking #Genomics #Bioinformatics @anitascoones.bsky.social @biorxiv-bioinfo.bsky.social 🧬 🖥️
www.biorxiv.org/content/10.1...

An optimised computational approach for the identification of somatic structural variants in cancer. #SomaticStructuralVariants #CancerGenetics #Genomics #Bioinformatics #ToolsBenchmarking @biorxiv-bioinfo.bsky.social 🧬 🖥️
www.biorxiv.org/content/10.1...