1 s improved TFBS identification in comparison to analyses using individual data sources or a simple me

2                         However, in contrast to analyses using peptide substrates, we find that the h

3 its and disease, but repeats are challenging to analyse using short-read sequencing technology.

4 sm (SNP) panel of 394 SNPs as an alternative to analyses using simple sequence length polymorphism (S

5 ease-discordant sibling pairs are equivalent to analyses using the SACO design.

6 arks and has, consequently, proved difficult to analyse using traditional 3D morphometric methods.