<p>The tree shows the divergence of CNVs present on 11q12 chromosomal location. (b) shows the tree constructed based on the OR4 gene family, which is distributed on different chromosomal locations. Both the trees were constructed by UPGMA method.</p
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
<p>Anatomically modern humans evolved from Africa formed the first settlement which branched further...
<p>(A) CRN genes with different C-terminal regions were shown to have nearly identical N-terminal se...
<p>a–d show the trees for the −1 kb upstream and downstream flanking sequences of the most common CN...
<p>a) CNV map of 379 shared CNVs across all chromosomes and populations<b>.</b> The outermost to inn...
<p>(A) A split tree inferred from the complete <i>N</i> gene sequence showing the evolutionary relat...
<p>The phylogenetic tree was constructed by the Neighbor-Joining method with 1000 bootstrap replicat...
Understanding variation in genome structure is essential to understand phenotypic differences within...
<p>Phylogenetic analysis of DENV-2 as determined from 14 ML trees derived from the complete genome, ...
<p>Phylogenetic analysis of DENV-1 as determined from 14 ML trees derived from the complete genome, ...
<p>Phylogeny tree of CCHFV sequences from India based on partial nucleocapsid gene.</p
<p>The letters (A, B, C... X) represent genes (or genomic regions) from a hypothetical viral genome....
<p>(<b>A</b>) Five mutually-exclusive gene categories based on orthology and paralogy: Non LSGs (Non...
Rare copy number variations (CNVs) generated by human genomic rearrangements have been shown to play...
<p>Phylogenetic tree of (a) TNFα and (b) IL10 nucleotide sequence constructed using Geneious Pro 5.6...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
<p>Anatomically modern humans evolved from Africa formed the first settlement which branched further...
<p>(A) CRN genes with different C-terminal regions were shown to have nearly identical N-terminal se...
<p>a–d show the trees for the −1 kb upstream and downstream flanking sequences of the most common CN...
<p>a) CNV map of 379 shared CNVs across all chromosomes and populations<b>.</b> The outermost to inn...
<p>(A) A split tree inferred from the complete <i>N</i> gene sequence showing the evolutionary relat...
<p>The phylogenetic tree was constructed by the Neighbor-Joining method with 1000 bootstrap replicat...
Understanding variation in genome structure is essential to understand phenotypic differences within...
<p>Phylogenetic analysis of DENV-2 as determined from 14 ML trees derived from the complete genome, ...
<p>Phylogenetic analysis of DENV-1 as determined from 14 ML trees derived from the complete genome, ...
<p>Phylogeny tree of CCHFV sequences from India based on partial nucleocapsid gene.</p
<p>The letters (A, B, C... X) represent genes (or genomic regions) from a hypothetical viral genome....
<p>(<b>A</b>) Five mutually-exclusive gene categories based on orthology and paralogy: Non LSGs (Non...
Rare copy number variations (CNVs) generated by human genomic rearrangements have been shown to play...
<p>Phylogenetic tree of (a) TNFα and (b) IL10 nucleotide sequence constructed using Geneious Pro 5.6...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
<p>Anatomically modern humans evolved from Africa formed the first settlement which branched further...
<p>(A) CRN genes with different C-terminal regions were shown to have nearly identical N-terminal se...