Even with the 1 million SNP coverage of the Illumina chip used in the present study with imputation of 7 million other SNPs, there is a high chance of missing potentially highly significant SNPs and this coverage is best suited to identify regions of the genome that associate with disease severity as opposed to identifying single SNPs.
← all excerpts
Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.
1
—
—