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'Contribution' scores for each sequence fragment were calculated as described previously (described there as 'agreement' scores) [46], [72].
Quantification was relative to a standard curve obtained with known amounts of FMDV C-S8c1 RNA, using a procedure that has been described previously described [58], [59].
Preparation of cells for morphology was performed as described previously described (Rieder et al., 1996).
Northern blots (van Rooij et al, 2008) to detect microRNAs were performed as described previously described.
The NMR measurements were essentially carried out as described previously described [ 8].
Staining for COX and SDH activity was carried out on cryosections, essentially as described previously described (76, see Supplementary Material, Fig. SI).
Similar(54)
CML T composites were synthesized as described by the method described previously (Yang et al. 2014) with minor modifications.
ST + HS was carried out using a hardware/software platform for computerized, closed-loop HS in mice described previously [21], described in greater detail in Document S1.
Sdh activity was measured as described previously [45] with modifications as described [46].
Network analysis was largely carried out as described previously [3], with modifications as described below.
Cryo-scanning electron microscopy and x-ray microanalysis was performed as described previously [9] with modifications described in Methods S1.
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