Sentence examples for both assemblies were then from inspiring English sources

The potentiometric responses of both assemblies were then measured as a function of urea concentration using a home-made portable potentiostat.

The individual assemblies were then merged using both Velvet and Oases to produce a single reference transcriptome.

The transcripts from the 6 assemblies were then pooled and re-assembled using CAP3 [ 39] to produce a meta-assembly.

The five SAGs Velvet assemblies were then merged and co-assembled using the de novo assembly algorithm implemented in Geneious (Biomatters Ltd ,Auckland NZ).

The assemblies were then concatenated and the pool of 138,954 transcripts was re-assembled using CAP3 [ 28].

For each sample (or pool), all (independently produced) partition assemblies were then concatenated.

Assemblies were then dialyzed against TBS to remove cholate and promote NLP self-assembly.

All these assemblies were then merged with Cuffmerge.

Reference and de novo assemblies were then concatenated.

These assemblies were then merged into a single assembly using the cuffmerge function from Cufflinks [ 60].

These assemblies were then merged together using the Cuffmerge utility [ 79], into a general transcriptome assembly.