Pinned Loading
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call_known_mutations_from_RNAseq
call_known_mutations_from_RNAseq PublicSome snippet of code to call mutations in single cells. The mutations are NOT called di novo, you need to have previously defined the variants in a VCF file. In the case of cancer, a good starting …
Shell
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scRNAseq-QC-alignment-and-quantification
scRNAseq-QC-alignment-and-quantification PublicPerform QC on single-cell_RNA_seq reads data, alignment and quantification
Shell
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single_cell_R_functions
single_cell_R_functions PublicA collection of R functions to manipulate single cell data
R
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