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1 ut GC-rich in the monocot genomes (59-61% of G+C content).
2 compact genome of 395,405 bp, with a 33.62% G+C content.
3 eighboring nucleotides and the overall local G+C content.
4 s a large (6.7 Mbp) genome with a high (67%) G+C content.
5 or the major cause of the diversities of the G+C content.
6 es are small and not correlated with the DNA G+C content.
7 only a minor effect, if any, on the average G+C content.
8 lower G+C content than the average aeromonad G+C content.
9 compositions at the extremes of high or low G+C content.
10 sms for splice site recognition depending on G+C content.
11 -bp spacers of arbitrary sequences with high G/C content.
12 by changing strand length, concentration and G/C content.
13 ing in an overall mutation pressure to lower G+C contents.
14 in bacterial species having widely different G+C contents.
15 ve codon use, is driving genes toward higher G+C contents.
16 1% of the genes, apparently due to shifts in G + C content.
17 regions - termed isochores - with differing G + C content.
18 st that selection is acting upon silent site G + C content.
19 Saccharomyces cerevisiae that share the same G + C content.
20 idelity, codon context, and global and local G + C content.
21 omes local CpG deficit decreases with higher G + C content.
22 alignments, and depend strongly on the local G + C content.
23 ar polysaccharide (CP) biosynthesis, and its G+C content (26.7%) is lower than the average G+C conten
25 ion of pColJs showed significantly different G+C content (34%) compared to the rest of pColJs (53%).
26 etween these IS elements has a wide range of G+C content (35 to 57%), suggesting that these regions h
27 bases (Mb), with a low guanine and cytosine (G + C) content, 35%; the coding sequences cloned to date
28 oplasma species, having reduced size and low G+C content (38.8% for M. haemofelis and 31.1% for M. su
29 7 was more prevalent in genomic regions with G+C content (50.5 to 60.5%) lower than the average G+C c
31 single circular chromosome of 2,501,097 bp (G+C content, 73%) predicted to encode 2,403 proteins.
32 ith siRNA functionality were identified: low G/C content, a bias towards low internal stability at th
35 ed vertebrates show large-scale variation in G + C content along their chromosomes, a pattern which a
39 ecies, with different selective pressures on G+C content among lineages, and compared the counts of n
41 he most precise and accurate available, with G + C content amplification biases less than 1.5-fold, e
42 quencing, and percent guanine-plus-cytosine (G+C) content analysis, demonstrated that these strains a
44 92, P < 0.001) among these genomes' intronic G + C contents and exonic G + C contents at degenerate t
45 ults showing that sapD and recA have similar G + C contents and substitution rates suggest that the s
47 the library was dominated by sequences whose G+C content and CpG frequency were intermediate between
48 are longer than 200 bp and have over 50% of G+C content and CpG frequency, at least 0.6 of that stat
49 sekeeping gene promoter, including very high G+C content and enzyme restriction sites characteristic
50 are consistent with the hypothesis that exon G+C content and intron U content contribute separate but
52 ted with precise hot-spot location, although G+C content and nucleotide diversity are correlated with
53 n a region of the Salmonella genome with low G+C content and presumably has been acquired by horizont
54 lated to gram-positive bacteria with low DNA G+C content and that its closest relative is Dehalobacte
56 o aspects: intragenomic heterogeneity of the G+C content and the amino-acid-specific translation-coup
57 ns into two classes according to their flank G+C content and used computational and statistical metho
61 can recognize miRNAs with different A/U and G/C content and distinguish between a fully matched miRN
63 oligo and salt concentrations, constraining G+C content, and introducing mismatches are exemplified.
64 xtremely high LINE and low SINE content, low G+C content, and yet a relatively high gene density, in
65 ether nucleotide substitution rates and gene G + C content are influenced by the chromosomal location
67 For both synonymous substitution rates and G + C content at silent sites, neighbouring genes were f
68 n increased usage of amino acids with a high G + C content at the first two codon positions and GNN c
70 by this compositional bias, with the average G+C content at synonymously variable third positions of
71 dence of an increase in third codon position G+C content at the start of genes; this is particularly
72 Finally, the overall % G+C content and the % G+C content at the third codon for all of the PKS genes
73 gerprint is similar in the wide range of the G+C content at the third codon position (0.30-0.80).
74 s of the same gene were correlated; but mean G+C content at the third positions of exons was signific
75 alogous regions of the chromosome with a low G+C content, at 41%, compared to that of the whole genom
76 is AU-rich in the eudicot genomes (35-42% of G+C content), but GC-rich in the monocot genomes (59-61%
77 that intrinsic sequence properties, such as G/C content, cannot fully explain plant nucleosome posit
80 promoter region revealed that it has a high G+C content, contains potential SP1 and AP1 binding moti
81 There are, however, genomic regions of high G+C content (CpG islands), where the occurrence of CpGs
82 clustered gene families, corresponding high G + C content, CpG islands and density of repetitive DNA
83 ty island (YP-HPI) is marked by IS100, has a G + C content different from its host, is flanked by 24
84 rizontal gene transfer in that their percent G+C content differs from that of the rest of the H. infl
85 3' end of tRNA(4)(Leu) and has regions whose G+C content differs from the average genomic G+C content
92 or other promoter cis elements and have high G+C content, functional Sp1 binding sites and multiple t
93 ely independent of the isochore compartment (G + C content), gene size, and transcriptional and trans
95 II secretion system were identified on a low-G+C-content genomic island containing 24 intact genes th
100 ate catabolite repression in a number of low-G+C-content gram-positive bacteria, of which C. perfring
103 The results show that genes in the different G+C content groups have similar PR2 biases, indicating t
105 pical of a housekeeping gene, including high G + C content, high frequency of CpG dinucleotides, and
106 frequency of optimal codons (Fopt) and gene G+C content, highlighting the G+C-biased gene conversion
110 nsible for the wide heterogeneity of the DNA G+C content in human, the third codon position of 846 hu
113 d) has shown that, in the major range of the G+C content in the third codon position (0.25-0.75), bia
115 elevated silent substitution rates and high G+C contents in comparison with both metatherian autosom
116 also a region of exceptionally high gene and G + C content including genes paralogous to those in the
120 f the C. burnetii genome is 42.4%, where the G+C content is 42.7% for the chromosome and 38.7% for th
124 g that the intragenomic heterogeneity of the G+C content is not correlated with translation-coupled b
125 monstrated that the regional similarities in G + C content (isochores) and synonymous substitution ra
129 Perhaps to accommodate DNA with a lower G + C content, most mycoplasmas do not have the "univers
132 in derived bacterial lineages, the inferred G + C content of ancient ribosomal RNA, and the geologic
133 spite predictions based primarily on the low G + C content of the chloroplast and the high functional
137 us sequence and prediction features, such as G + C content of the sequence, length and type of exons,
138 repeat of Alces-I has a length of 968 bp, a (G + C) content of 52.6%, and contributes 35%, or almost
139 mid of Borrelia burgdorferi had 16,927 bp, a G+C content of 23.1%, a relative deficiency of CpG dinuc
141 e draft genome of strain NSH-16(T) has a DNA G+C content of 27.4% and an approximate size of 3.2 Mb.
144 5, consisting of approximately 2.9 Mb with a G+C content of 35% and 2,704 genes, was annotated using
152 65,009-nucleotide sequence, with an overall G+C content of 42.6%, revealed genes and open reading fr
156 84,406 base pairs in length, with an overall G+C content of 51.8%, and contains 2,121 predicted codin
160 m those of all other EEHVs by 37% and have a G+C content of 63% compared to just 42% for the others.
163 The first method was to plot the average G+C content of a set of nucleotides against the G+C cont
166 ontribution of mutation and selection to the G+C content of DNA was analyzed in bacterial species hav
167 e amino acid specific and independent of the G+C content of DNA, so that when averaged over the amino
170 nly 25.5% G+C in nucleotide content, and the G+C content of individual genes may predict how essentia
172 teins of known function; of these, 18 have a G+C content of less than 40%, typical of known virulence
175 transcription start sites suggests that the G+C content of the -10 region is higher than that for E.
182 e genes (26%) differs significantly from the G+C content of the entire C. jejuni genome (30.6%).
183 ent Yersinia isolates and the relatively low G+C content of the gene suggests acquisition by horizont
185 Despite the considerable differences in G+C content of the macaque and B virus genes (51% and 74
186 the majority of species, in some species the G+C content of the minor class of genes distributes over
187 In particular, we propose that the higher G+C content of the Monodelphis X chromosome is a direct
188 etected in related bacterial species and the G+C content of the pcgL-containing region (41%) is much
189 nsposon-like structures, corroborated by the G+C content of the pJM1 sequence, suggest a modular comp
193 content of a set of nucleotides against the G+C content of the third codon position for each gene.
194 are all correlated almost perfectly with the G+C content of the third codon position over the total G
195 separated into six groups according to their G+C content of the third codon position, and each group
198 revealed by the relative independence of the G+C content of the third codon positions from the isocho
201 hereas intragenomic distributions of the DNA G+C content of these bacteria are narrow in the majority
204 cted by plotting PR2 corollaries against the G+C content of third codon position revealed that eight
206 its among major phylogenetic groups, and the G+C contents of the chromosome (69.2%) and plasmid (66%)
214 of the phased A/T motifs or lowering of the G/C content of the spacers resulted in a reduction in Rt
215 It was discovered that modification of the G:C content of the anticodon stem and therefore reducing
216 tautp decreased roughly linearly with the G:C content of the hairpin helix, being 50% longer for h
219 o tRNA genes, and have diverged widely, with G+C contents ranging from 40 to 70% and amino acid homol
225 ence of this region reveals a relatively low G+C content, remnants of transposons, and several open r
227 Conversely, D increased linearly with helix G:C content, roughly doubling as the G:C content increas
229 mobile genetic element sequences and have a G + C content significantly lower than the rest of the H
230 istic of the genome of organisms with a high G+C content, such as P. aeruginosa, suggesting that IncP
231 an both Arthrobacter genomes and has a lower G+C content, suggesting that significant genome reductio
232 long with their similar codon usage bias and G + C content, suggests acquisition by lateral transfer
233 provements are observed when amplifying high G+C content templates, such as those belonging to the pr
235 gestion with MspI have an average of 5% more G + C content than the random fragments, and are enriche
236 oximately 150 kilobases in size, has a lower G + C content than the rest of the genome, and is flanke
238 cks were found to have a significantly lower G+C content than non-vector-borne flaviviruses and this
240 was attributable to genes with unusually low G+C content that are probably due to horizontal transfer
241 group B shows two new large regions with low G+C content that are putative pathogenicity islands.
243 own dependence of DNA melting temperature on G.C content, the contribution of base-pairing into duple
244 imposed by error-prone replication, (b) high G + C content to increase replication fidelity, (c) circ
247 in Arabidopsis thaliana tend to have higher G/C content, unlike yeast, and are centered on specific
251 ons between mouse and rat; but the change in G+C content was greatest at position 3 of exons, interme
252 on if a common sequence with high or average G/C content was present immediately upstream of the AU-r
254 , mosquito-borne viruses had an intermediate G+C content which was not significantly different from t
255 ticellular organism are heterogeneous in the G+C content, which is particularly true in the third cod
256 .71 generally fit to a linear dependence on (G+C)-content, which, however, is consistent with a (G+C)
257 We report a list of loci that have different G+C content with respect to the nearby regions; the anal
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