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These complementary sequences could form a stem that served to bring the splice sites into proximity and thereby promote splice site pairing.
This detection was rendered possible by the highly complementary 5′- and 3′-sequences that viral ssRNAs contain because these highly complementary sequences could form short double-stranded structures with perfectly blunt ends.
The 34 pre-miRNA sequences could form hairpin structures as predicted by MFOLD.
This analysis revealed that these BioH sequences could form three families, designated I, II, and III.
The paired inverted sequences could form the stem of the hairpin.
One hundred and fourteen chromosomal regions, which correspond to 40 cloned sequences, could form a stable hairpin structure.
Similar(51)
The hybridization events were evaluated by ECL measurements and only the complementary sequence could form a double-stranded DNA (dsDNA) with DNA probe and give strong ECL signals.
The results showed that only a complementary sequence could form a dsDNA with the Cu-DNCs DNA probe and give an obvious electrochemical signal.
As a result, a new inverted repeat sequence could form, as explained in Fig. 4.
To analyze whether the matched sequence could form a suitable hairpin (the secondary structure of the small RNA precursor), sequences surrounding the matched sequence were extracted.
To analyze whether the matched sequence could form a suitable hairpin, sequences surrounding the matched sequence (100~200 nt to either side) were extracted and run through RNAfold.
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