Life as we see it in our planet today has been shaped by many different biological processes, particularly natural selection, during billions of years. These processes leave a signature in our genomes in the form of differences between species, or between individuals of the same species. Interrogating these patterns of genome diversity we can infer what are the forces that affect living organisms, how and when they act and how do they affect such various things as biodiversity, human emotions or the differential susceptibility of different persons to certain diseases. All this knowledge empowers us to control our future but, above all, it is very fun to obtain.

Currently, the main research goals of the group focus on to elucidating how evolution, and particularly natural selection, has shaped genome and phenotype diversity in our lineage. To this end, we combine experiments, models and data analysis. Some specific research lines are as follows:


Chromosomal evolution and speciation 

We study how large chromosomal rearrangements affect many aspects of genome structure and evolution, including how they may drive the generation of new species.


Segmental duplications and copy-number variation in primates 

The genomes of humans and other primates show an enrichment in Segmental Duplications (SDs) with high sequence identity, plus they present may Copy-Number Variants (CNVs), large genome fragments of which different individuals present different copies. SDs and CNVs are fundamental for the creation of novel genes and may have been key in the evolution of our lineage. We study not only the frequencies and genome locations of these variants, but also the molecular evolution of their sequence content.


Detecting the genomic signature of natural selection 

We try to detect the signature of adaptive changes out of single-copy protein-coding regions. We focus in how natural selection may have shaped variability patterns in introns and regulatory regions of genes.


Human disease and its evolutionary implications 

We study world-wide patterns of disease susceptibility distribution to ascertain how these may have been influenced by recent human evolution. In addition, we investigate the possible origins of Multiple Sclerosis and its possible relationship with very recent natural selection events in humans.



Complex human traits that are exclusive of our lineage are the basis of our societies and have huge socio-economic impact. We deploy the latest tools of genomics for the dissection of human economic traits.


Lab website: Evolutionary Genomics Lab

Investigador principal Investigador principal

Membres del grup Membres del grup

Projectes en curs Projectes en curs

Publicacions Publicacions

Petit, N.; Piñeyro, D.; López, E.; Casacuberta, E.; Navarro, A.  2012. HeT_A_pi1, a piRNA target sequence in the Drosophila telomeric retrotransposon HeT-A is extremely conserved across copies and species. PLOS ONE 7 (5): e37405.

Lorente-Galdós, B.; Medina, I.; Morcillo-Suárez, C.; [5 authors]; Pisano, D.G.; Dopazo, J.; Navarro, A.  2012. SYSNPs (Select Your SNPs): a web tool for automatic and massive selection of SNPs. International Journal of Data Mining and Bioinformatics 6 (3): 324-334.

Garcia-Mas, J.; Benjak, A.; Sanseverino, W.; [21 authors]; Navarro, A.; Marquès-Bonet, T.; [6 authors]; Casacuberta, J.M; Arús, P.; Puigdomènech, P.  2012. The genome of melon (Cucumis melo L.). Genome amplification in the absence of recent duplication in an old widely cultivated species. Proceedings of the National Academy of Sciences USA 109 (29): 11872-11877.

Dickhaus, T.; Straiburger, K.; Schunk, D.; Morcillo-Suárez, C.; Illig, T.; Navarro, A.  2012. How to analyze many contingency tables simultaneously in genetic association studies. Statistical Applications in Genetics and Molecular Biology 11 (4): ISSN (Online) 1544-6115.

Cant, E.; Reverter, F.; Morcillo-Suárez, C.; [10 authors]; Navarro, A.; [4 authors];Tintor M.; Montalban, X.; Comabella, M.  2012. Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis. Multiple Sclerosis Journal 18 (7): 983-990.