<p><b>(A)</b> Comparison of π in different genomic regions. The values were normalized with that of intronic regions. <b>(B)</b> The ratios of π for non-synonymous sites to synonymous sites for <i>de novo</i> genes or orthologs in rhesus macaque were summarized in boxplots (<b>C-F</b>) Derived allele spectra for <i>de novo</i> genes (<b>C</b>), protein-coding genes (<b>E</b>) and lncRNAs (<b>F</b>) in human, as well as for the macaque regions orthologous to the human <i>de novo</i> genes (<b>D</b>) are shown. The standard deviations estimated by 1,000 bootstrap replicates are indicated by the error bars.</p
By studying the patterns of nucleotide variation in conserved non-coding (CNC) sequences in comparis...
Published estimates of the proportion of positively selected genes (PSGs) in human vary over three o...
The birth of new genes is an important motor of evolutionary innovation. Whereas many new genes aris...
<p><b>(A)</b> GC contents for randomly-selected intergenic regions, all lncRNAs and lncRNA precursor...
<p>(<b>A</b>) Computational pipeline for <i>ab inito</i> identification and meta-analysis of <i>de n...
<p><b>(A)</b> Comparison of human polymorphism sites profiled in this study with those in the 1000 G...
<p>(A) Summed RPKM scores (log<sub>2</sub> transformed) of <i>de novo</i> genes in seven tissues fro...
<p><b>a)</b> Simplified phylogenetic tree indicating the nine species considered in this study. In a...
<div><p>While some human-specific protein-coding genes have been proposed to originate from ancestra...
<p>LncRNAs correspond to Gencode v13 (human) and protein coding genes to Refseq 57 (human, 20,848 ge...
<p>(A) Hierarchical clustering chart of tissue expression proportions. For each gene in one species,...
While some human-specific protein-coding genes have been proposed to originate from ancestral lncRNA...
<p><b>a)</b> Overrepresented transcription factor binding sites (TFBS) in the region -100 to 0 with ...
<p>(<b>A</b>) The percentages of macaque editing sites with corresponding editing sites in human and...
BACKGROUND: The identification of signatures of natural selection has long been used as an approach ...
By studying the patterns of nucleotide variation in conserved non-coding (CNC) sequences in comparis...
Published estimates of the proportion of positively selected genes (PSGs) in human vary over three o...
The birth of new genes is an important motor of evolutionary innovation. Whereas many new genes aris...
<p><b>(A)</b> GC contents for randomly-selected intergenic regions, all lncRNAs and lncRNA precursor...
<p>(<b>A</b>) Computational pipeline for <i>ab inito</i> identification and meta-analysis of <i>de n...
<p><b>(A)</b> Comparison of human polymorphism sites profiled in this study with those in the 1000 G...
<p>(A) Summed RPKM scores (log<sub>2</sub> transformed) of <i>de novo</i> genes in seven tissues fro...
<p><b>a)</b> Simplified phylogenetic tree indicating the nine species considered in this study. In a...
<div><p>While some human-specific protein-coding genes have been proposed to originate from ancestra...
<p>LncRNAs correspond to Gencode v13 (human) and protein coding genes to Refseq 57 (human, 20,848 ge...
<p>(A) Hierarchical clustering chart of tissue expression proportions. For each gene in one species,...
While some human-specific protein-coding genes have been proposed to originate from ancestral lncRNA...
<p><b>a)</b> Overrepresented transcription factor binding sites (TFBS) in the region -100 to 0 with ...
<p>(<b>A</b>) The percentages of macaque editing sites with corresponding editing sites in human and...
BACKGROUND: The identification of signatures of natural selection has long been used as an approach ...
By studying the patterns of nucleotide variation in conserved non-coding (CNC) sequences in comparis...
Published estimates of the proportion of positively selected genes (PSGs) in human vary over three o...
The birth of new genes is an important motor of evolutionary innovation. Whereas many new genes aris...