scholarly article | Q13442814 |
P819 | ADS bibcode | 2009PLoSO...4.8113B |
P356 | DOI | 10.1371/JOURNAL.PONE.0008113 |
P8608 | Fatcat ID | release_t2zbtkfyunb57dgdh4thodumjm |
P932 | PMC publication ID | 2781299 |
P698 | PubMed publication ID | 19956556 |
P5875 | ResearchGate publication ID | 40443638 |
P50 | author | Eystein Skjerve | Q82949199 |
Jon Bohlin | Q42322490 | ||
P2860 | cites work | Accelerated evolution associated with genome reduction in a free-living prokaryote | Q21999766 |
The genome of the heartwater agent Ehrlichia ruminantium contains multiple tandem repeats of actively variable copy number | Q22066393 | ||
The complete genome sequence of the gram-positive bacterium Bacillus subtilis | Q22122360 | ||
Evidence for lateral gene transfer between Archaea and Bacteria from genome sequence of Thermotoga maritima | Q22122435 | ||
Environments shape the nucleotide composition of genomes | Q24489465 | ||
The codon Adaptation Index--a measure of directional synonymous codon usage bias, and its potential applications | Q24498207 | ||
GeneMark.hmm: new solutions for gene finding | Q24546288 | ||
RNAmmer: consistent and rapid annotation of ribosomal RNA genes | Q24675768 | ||
Global features of sequences of bacterial chromosomes, plasmids and phages revealed by analysis of oligonucleotide usage patterns | Q24794642 | ||
Long-range periodic patterns in microbial genomes indicate significant multi-scale chromosomal organization. | Q25256794 | ||
Evidence of host-virus co-evolution in tetranucleotide usage patterns of bacteriophages and eukaryotic viruses | Q25257897 | ||
Basic local alignment search tool | Q25938991 | ||
Origin of replication in circular prokaryotic chromosomes | Q28292592 | ||
Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography | Q28764545 | ||
Amelioration of bacterial genomes: rates of change and exchange | Q29618260 | ||
Application of tetranucleotide frequencies for the assignment of genomic fragments | Q33205791 | ||
Reliability and applications of statistical methods based on oligonucleotide frequencies in bacterial and archaeal genomes | Q33321678 | ||
Investigations of oligonucleotide usage variance within and between prokaryotes | Q33329084 | ||
Global dinucleotide signatures and analysis of genomic heterogeneity | Q33538671 | ||
Nitrogen-fixing aerobic bacteria have higher genomic GC content than non-fixing species within the same genus. | Q52904226 | ||
Base composition bias might result from competition for metabolic resources. | Q52940121 | ||
Sequence-dependent DNA structure: dinucleotide conformational maps | Q73329866 | ||
Sequence-dependent DNA structure: the role of the sugar-phosphate backbone | Q74781286 | ||
Enzymatic synthesis of deoxyribonucleic acid. VIII. Frequencies of nearest neighbor base sequences in deoxyribonucleic acid | Q79125877 | ||
GC content and genome length in Chargaff compliant genomes | Q79437562 | ||
Formation and positioning of nucleosomes: effect of sequence-dependent long-range correlated structural disorder | Q82548023 | ||
Codon usage between genomes is constrained by genome-wide mutational processes | Q33976278 | ||
Microbial minimalism: genome reduction in bacterial pathogens | Q34118332 | ||
Dinucleotide relative abundance extremes: a genomic signature | Q34289038 | ||
Evolutionary implications of microbial genome tetranucleotide frequency biases | Q34373303 | ||
Involvement of DNA curvature in intergenic regions of prokaryotes | Q34594691 | ||
Bacterial pathogenomics | Q34702436 | ||
Compositional biases of bacterial genomes and evolutionary implications | Q35624486 | ||
Genomic GC level, optimal growth temperature, and genome size in prokaryotes. | Q36525252 | ||
Detecting horizontally transferred and essential genes based on dinucleotide relative abundance | Q36955997 | ||
Bacterial genome sequencing and its use in infectious diseases | Q36982025 | ||
Mono- through hexanucleotide composition of the Escherichia coli genome: a Markov chain analysis | Q40565882 | ||
An environmental signature for 323 microbial genomes based on codon adaptation indices | Q42093922 | ||
Reconstructing the ancestor of Mycobacterium leprae: the dynamics of gene loss and genome reduction. | Q42107461 | ||
Identification of coding and non-coding sequences using local Holder exponent formalism | Q42665584 | ||
Ecophysiological significance of scale-dependent patterns in prokaryotic genomes unveiled by a combination of statistic and genometric analyses | Q43736629 | ||
Bias of purine stretches in sequenced chromosomes | Q44080398 | ||
Aerobiosis increases the genomic guanine plus cytosine content (GC%) in prokaryotes | Q44108765 | ||
Seven GC-rich microbial genomes adopt similar codon usage patterns regardless of their phylogenetic lineages | Q47562989 | ||
Determination of bias in the relative abundance of oligonucleotides in DNA sequences | Q49219229 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | prokaryotes | Q19081 |
P304 | page(s) | e8113 | |
P577 | publication date | 2009-12-02 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Examination of genome homogeneity in prokaryotes using genomic signatures | |
P478 | volume | 4 |
Q34001815 | A quantitative account of genomic island acquisitions in prokaryotes |
Q33851538 | Across bacterial phyla, distantly-related genomes with similar genomic GC content have similar patterns of amino acid usage |
Q34904516 | Amino acid usage is asymmetrically biased in AT- and GC-rich microbial genomes. |
Q33657435 | Genomic comparisons of Brucella spp. and closely related bacteria using base compositional and proteome based methods |
Q46361707 | Insights from the complete genome sequence of Clostridium tyrobutyricum provide a platform for biotechnological and industrial applications |
Q35074674 | Microbial genomic taxonomy |
Q33688556 | Natural selection retains overrepresented out-of-frame stop codons against frameshift peptides in prokaryotes |
Q41303342 | Phylogenomic Analysis of Oenococcus oeni Reveals Specific Domestication of Strains to Cider and Wines |
Q34156218 | Relative entropy differences in bacterial chromosomes, plasmids, phages and genomic islands |
Q34442010 | Stoichiogenomics: the evolutionary ecology of macromolecular elemental composition |
Q36277287 | The nucleotide composition of microbial genomes indicates differential patterns of selection on core and accessory genomes. |
Search more.