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The ROTEM device was checked for correct functioning according to the manufacturer's recommendation by using control plasma (ROTROL N).
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All imagery was visually checked for correct plaque detection.
Each matched record was checked for correct identification.
In addition, exons were checked for correct ordering and strand.
All frames were checked for correct tracing and manually corrected if needed.
The PCR products were again checked for correct size and purity.
The remaining SNPs were checked for correct clustering by Illumina's GenomeStudio software.
All transformants were checked for correct genome integration by genomic PCR.
Neo-resistant clones were checked for correct integration of the targeting vector by PCR.
They were checked for correct grammar and typography by a secretary.
Ends were checked for correct PCR primer using fastx_barcode_splitter (http://hannonlab.cshl.edu/fastx_toolkit/index.html).html
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CEO of Professional Science Editing for Scientists @ prosciediting.com