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Suppose we have a matrix of single-cell RNA-seq data that looks like this:
zcat exprMatrix.tsv.gz | head | cut -f1-5
gene sci3-me-001.GTCGGAGTTTGAGGTAGAA sci3-me-001.ATTAGTCTGTGTATAATACG sci3-me-001.GAGGAACTTAATACCATCC sci3-me-001.TTCGCGGATACTCTCTCAA
ENSMUSG00000051951.5|Xkr4 0 0 0 0
ENSMUSG00000103377.1|Gm37180 0 0 0 0
ENSMUSG00000104017.1|Gm37363 0 0 0 0
ENSMUSG00000103025.1|Gm37686 0 0 0 0
ENSMUSG00000089699.1|Gm1992 0 0 0 0
ENSMUSG00000103201.1|Gm37329 0 0 0 0
ENSMUSG00000103161.1|Gm38148 0 0 0 0
ENSMUSG00000102331.1|Gm19938 0 0 0 0
ENSMUSG00000102343.1|Gm37381 0 0 0 0
Rows:
zcat exprMatrix.tsv.gz | wc -l
26184
Columns:
zcat exprMatrix.tsv.gz | head -n1 | wc -w
2058653
Could I please ask if you might be able to share an R code snippet for how to use the beachmat package to read this data into a sparse matrix (dgCMatrix)?
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