The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we report the sequencing and comparative analysis of 29 eutherian genomes. We confirm that at least 5.5% of the human genome has undergone purifying selection, and locate constrained elements covering ∼4.2% of the genome. We use evolutionary signatures and comparisons with experimental data sets to suggest candidate functions for ∼60% of constrained bases. These elements reveal a small number of new coding exons, candidate stop codon readthrough events and over 10,000 regions of overlapping synonymous constraint within protein-coding exons. We find 220 candidate RNA structural families, and nearly a million elements overlapping potential promote...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases and meas...
Comparative genomics allow us to search the human genome for segments that were extensively changed ...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases, and mea...
The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we ...
The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we ...
Ten years on from the finishing of the human reference genome sequence, it remains unclear what frac...
Ten years on from the finishing of the human reference genome sequence, it remains unclear what frac...
Comparative genomics allow us to search the human genome for segments that were extensively changed ...
Zoonomia is the largest comparative genomics resource for mammals produced to date. By aligning geno...
Zoonomia is the largest comparative genomics resource for mammals produced to date. By aligning geno...
Background: Different regions in a genome evolve at different rates depending on structural and func...
A key component of the ongoing ENCODE project involves rigorous comparative sequence analyses for th...
A key component of the ongoing ENCODE project involves rigorous comparative sequence analyses for th...
Background: Different regions in a genome evolve at different rates depending on structural and func...
Abstract Background Different regions in a genome evolve at different rates depending on structural ...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases and meas...
Comparative genomics allow us to search the human genome for segments that were extensively changed ...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases, and mea...
The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we ...
The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we ...
Ten years on from the finishing of the human reference genome sequence, it remains unclear what frac...
Ten years on from the finishing of the human reference genome sequence, it remains unclear what frac...
Comparative genomics allow us to search the human genome for segments that were extensively changed ...
Zoonomia is the largest comparative genomics resource for mammals produced to date. By aligning geno...
Zoonomia is the largest comparative genomics resource for mammals produced to date. By aligning geno...
Background: Different regions in a genome evolve at different rates depending on structural and func...
A key component of the ongoing ENCODE project involves rigorous comparative sequence analyses for th...
A key component of the ongoing ENCODE project involves rigorous comparative sequence analyses for th...
Background: Different regions in a genome evolve at different rates depending on structural and func...
Abstract Background Different regions in a genome evolve at different rates depending on structural ...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases and meas...
Comparative genomics allow us to search the human genome for segments that were extensively changed ...
Noncoding DNA is central to our understanding of human gene regulation and complex diseases, and mea...