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These models vary in complexity, ranging from the treatment of insertion and deletion events (indels) as single-nucleotide events [ 13] to the modeling of complex length distributions for indels [ 9, 14, 15], but all allow for evolutionary inference without assuming a single alignment.
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Four items including A2 (reasoning of treatment), B3 (depth of insertion), D1 (details of other treatments) and D2 (setting and context) were reported in less than half of component studies in the Cochrane reviews and of RCTs.
To identify genes enriched in mutations following carboplatin treatment, the number of insertion sites per gene was compared to an unselected mutagenized population (Carette et al, 2011) using a one-sided Fisher exact test.
This recommendation is based on various studies which show that the incidence of catheter-associated primary bloodstream infection can be significantly reduced when CHG is used for treatment of the catheter insertion site [ 1].
Due to uncertainty as to whether the micro-column experiment was capturing the same precipitation processes as the larger column, a sub-core was extracted from the large column after completion of the urea treatment by insertion of rigid polycarbonate tubing.
The preferred treatment is insertion of a shunt for drainage of cerebrospinal fluid (CSF), which gives good clinical results and a favourable complication profile [ 2, 3].
Immediate treatment involved insertion of a temporary cardiac pacemaker; this was succeeded by β-adrenergic blocker maintenance therapy.
The surgical treatment was insertion of a ventricular-peritoneal (VP) shunt with a HAKIM™ programmable valve shunt system (Codman & Shurtleff, Inc. Le Locle, Switzerland), with an opening pressure at implantation of 12 cm H2O.
Surface biotinylation demonstrated mERα in both female and male astrocytes, but only in female astrocytes did estradiol treatment increase insertion of the receptor into the membrane, a necessary step for maximal [Ca2+]i release.
There is no evidence to support the routine use of narcotics for the treatment of pain after IUC insertion, and therefore, it is not recommended.
Poly-A treatment, insertion of the PCR products into pDrive vector, transformation of E. coli EZ competent cells (Qiagen) and cloning were performed using a PCR Cloning Kit (Qiagen) as described by the supplier.
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