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Sequences were verified and both strands were assembled using the STADEN package [89].
Both strands were assembled using the Staden Package.
Sequence reads derived from both strands were assembled, aligned, and analyzed for nucleotide differences using Sequencher v4.8 (GeneCodes).
Sequences from both strands were assembled and edited in Sequencher 4.6 (Gene Codes Corporation, Ann Arbor, Michigan, USA).
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The sequences of two strands were assembled into double-stranded contig using Sequencher software (Gene Codes, Ann Arbor, Michigan, USA).
Eleven of these strands were assembled to a cable.
Raw sequence chromatograms of forward and reverse strands were assembled in Seqman II (DNASTAR, Inc., Madison, WI, USA).
Forward and reverse strands were assembled for each individual sample in the SEQMANII version 3.6.0 (DNASTAR , Inc.
Forward and reverse strands were assembled using CodonCode Aligner version 2.0.1 [ 53].
Using this method, AuNSs of different sizes ranging from 15 to 80 nm with complementary DNA strands were assembled on the Au hemisphere of a 160 nm JNP, with well-controlled structure and yield.
The rods in the strands are assembled in a helical fashion and likewise the strands in the tether are assembled with a helix.
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