Library 4 was a multiplex sequencing library of nine equimolar indexed samples, which was enriched using one target enrichment reaction.
Library 3 was a multiplex sequencing library of three equimolar indexed samples, which was enriched using one target enrichment reaction.
These finished libraries were enriched using the Nimblegen SeqCap kit.
Lymphocytes and single cells were enriched using light-scatter.
Low abundance proteins were enriched using a bead-based combinatorial library of hexapeptides.
For this reason, total DJ-1 (MW~19.9 kDa) was enriched using differential solubilization (DS) methods before being submitted to MS for identification.
Salusin-β immobilized on each sepharose gel was first placed in contact with solubilized membrane protein fractions enriched using a detergent20.
Samples collected for low-abundance protein analysis were fractionated, enriched using ProteoMiner treatment, and separated using sodium dodecyl sulfate-PAGE.
The PCSK9 and LAMP-2 expression networks were designed with Cytoscape software and, were enriched using transcription factor databases.
The pathway terms were enriched using the KEGG orthology based annotation system (KOBAS).
