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Recent "Conserved" articles

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Systematic discovery of regulatory motifs in conserved regions of the human genome, including thousands of CTCF insulator sites
Xiaohui Xie et al.
Proceedings of the National Academy of Sciences of the United States of America 104 (17), 0701811104-0701817150 (18 Apr 2007)
 
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
Adam Siepel et al.
Genome Research 15 (8), 1034-3715005 (15 Jul 2005)
We have conducted a comprehensive search for conserved elements in vertebrate genomes, using genome-wide multiple alignments of five vertebrate species (human, mouse, rat, chicken, and Fugu rubripes). Parallel searches have been performed with multiple alignments of four insect species (three species of Drosophila and Anopheles gambiae), two species of Caenorhabditis, and seven species of Saccharomyces. Conserved elements were identified with a computer program called phastCons, which is based on a two-state phylogenetic hidden Markov model (phylo-HMM). PhastCons works by fitting a phylo-HMM to the data by maximum likelihood, subject to constraints designed to calibrate the model across species groups, and then predicting conserved elements based on this model. The predicted elements cover roughly 3%-8% of the human genome (depending on the details of the calibration procedure) and substantially higher fractions of the more compact Drosophila melanogaster (37%-53%), Caenorhabditis elegans (18%-37%), and Saccharaomyces cerevisiae (47%-68%) genomes. From yeasts to vertebrates, in order of increasing genome size and general biological complexity, increasing fractions of conserved bases are found to lie outside of the exons of known protein-coding genes. In all groups, the most highly conserved elements (HCEs), by log-odds score, are hundreds or thousands of bases long. These elements share certain properties with ultraconserved elements, but they tend to be longer and less perfectly conserved, and they overlap genes of somewhat different functional categories. In vertebrates, HCEs are associated with the 3? UTRs of regulatory genes, stable gene deserts, and megabase-sized regions rich in moderately conserved noncoding sequences. Noncoding HCEs also show strong statistical evidence of an enrichment for RNA secondary structure.
 
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
Adam Siepel et al.
Genome Research 15 (8), 1034-3715005 (15 Jul 2005)
 
Trade-offs in detecting evolutionarily constrained sequence by comparative genomics.
TRADEOFFS IN DETECTING EVOLUTIONARILY CONSTRAINED SEQUENCE BY COMPARATIVE GENOMICS
Annual Review of Genomics and Human Genetics 6 (1), 143 (2005)
 
ddbRNA: detection of conserved secondary structures in multiple alignments.
Diego di Bernardo, Thomas Down, and Tim Hubbard
Bioinformatics (Oxford, England) 19 (13), 1606-11 (01 Sep 2003)
 
Thousands of corresponding human and mouse genomic regions unalignable in primary sequence contain common RNA structure.
Elfar Torarinsson et al.
Genome Research 16 (7), 885-9 (01 Jul 2006)
 
RNAs everywhere: genome-wide annotation of structured RNAs.
Rolf Backofen et al.
J Exp Zoolog B Mol Dev Evol 308B (1), 1-25 (14 Dec 2006)
 
RNAProfile: an algorithm for finding conserved secondary structure motifs in unaligned RNA sequences.
Nucleic Acids Research 32 (10), 3258-69 (15 Jun 2004)
 
Adaptive Evolution of Conserved Noncoding Elements in Mammals
Su Kim and Jonathan Pritchard
PLoS Genetics 3 (9), 147 (01 Sep 2007)
 
Unproductive splicing of SR genes associated with highly conserved and ultraconserved DNA elements.
Liana Lareau et al.
Nature 446 (7138), 926-9 (19 Apr 2007)

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