Although copy number variants (CNVs) are important in genomic medicine, CNVs have not been systematically assessed for many complex traits. Several large rare CNVs increase risk for schizophrenia (SCZ ...

Create an rng object with np.random.default_rng(), you can seed it for reproducible results. You can draw samples from probability distributions, including from the binomial and normal distributions.

Genetic diseases arising from microdeletions and microduplications lead to copy number alterations of genomic regions containing one or more genes. Clinically, these rearrangements may be detected by ...

• PowerShell allows the creation and manipulation of arrays, which store multiple values in a single variable. Each item in the array can be accessed individually using its position number. • Arrays ...

I'm making a script that will write a two-dimensional array to an Excel spreadsheet. The script is meant to be called from within other scripts. An outer loop runs once for every row in the array. An ...