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The analysis was carried out over two times points in culture and clones were designated as either having 'high' or 'low' clipping phenotypes.
The clones were designated as p-15b16QTBP, p-15b59QTBPQTBP.
At this phase of isolation, individual clones were designated as HM3 human MSC cell lines.
After selecting with 0.1 µg/ml of puromycin/ml, the resulting clones were designated RKO-A3 WT-myc, ZFm1-myc, ZFm2-myc, and ZFm1&2-myc, respectively.
AGS clones were designated AGSI and MDA468 clones were designated Pim.
These clones were designated as "species" in our analyses.
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F1 diapausing eggs and F1 clones are designated as selfed or outcrossed depending on the type of cross that originated them.
The plasmid clones carrying the AS fragments from the HooFos09, HylFos15, and NomFos1B3 clones are designated HooCam09, HylCam15, and NomCam1B3, respectively.
These clones are designated "M" for mixed template while those TPS cloned from individual tissues are labeled with the single letter abbreviations described above (Table 1, Table 2, Table 3, and Table 4).
Clones are designated as aggregate-positive if they contain SDS-stable Sup35 NM aggregates that are detectable in the undiluted sample and at least 1 of the 3 two-fold serial dilutions, as analyzed by filter retention.
Areas on the chromosome delineated either by 13 or more clones, 3 clones, or one clone were designated as regions, clusters, or orphans, respectively.
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