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CNVkit Sex (version 0.9.12+galaxy0)
Copy number cnn or copy ratio cnr files
Assume inputs were normalized to a male reference
Guess samples’ chromosomal sex from the relative coverage of chromosomes X and Y. The output is a table of the sample name (derived from the filename), inferred sex (string “Female” or “Male”), and log2 ratio value of chromosomes X and Y.

Bin-level log2 ratios (.cnr)

Tabular file containing normalized log2 ratios for small genomic bins (divided regions of the genome). Used to detect raw copy number variations (CNVs) before segmentation.

chromosome Genomic chromosome (e.g., chr1, chrX)
start Start position of the bin.
end End position of the bin.
gene Gene name(s) overlapping the bin (if applicable).
log2 Normalized log2 ratio (sample coverage / reference coverage).
depth Average read depth in the bin.
weight Reliability weight of the bin (higher = more reliable).