| Cryptic species as a window into the paradigm shift of the species concept |
72 |
| Counting with DNA in metabarcoding studies: How should we convert sequence reads to dietary data? |
55 |
| Comparing methods for detecting multilocus adaptation with multivariate genotype-environment associations |
51 |
| Stacks 2: Analytical methods for paired-end sequencing improve RADseq-based population genomics |
45 |
| Scaling up: A guide to high-throughput genomic approaches for biodiversity analysis |
36 |
| How quantitative is metabarcoding: A meta-analytical approach |
34 |
| The choice of universal primers and the characteristics of the species mixture determine when DNA metabarcoding can be quantitative |
29 |
| The impact of transposable elements in adaptive evolution |
28 |
| These aren't the loci you'e looking for: Principles of effective SNP filtering for molecular ecologists |
26 |
| Gene flow and genetic drift in urban environments |
26 |
| Rates of gut microbiome divergence in mammals |
25 |
| Genome-based estimates of fungal rDNA copy number variation across phylogenetic scales and ecological lifestyles |
24 |
| Body size determines soil community assembly in a tropical forest |
24 |
| Asymmetric oceanographic processes mediate connectivity and population genetic structure, as revealed by RADseq, in a highly dispersive marine invertebrate (Parastichopus californicus) |
24 |
| The search for loci under selection: trends, biases and progress |
24 |
| The role of gene flow in rapid and repeated evolution of cave-related traits in Mexican tetra, Astyanax mexicanus |
23 |
| Going beyond SNPs: The role of structural genomic variants in adaptive evolution and species diversification |
22 |
| Evolution of heat-shock protein expression underlying adaptive responses to environmental stress |
21 |
| Extra-pair paternity in birds |
20 |
| Virus-virus interactions and host ecology are associated with RNA virome structure in wild birds |
20 |
| Demographic and genetic approaches to study dispersal in wild animal populations: A methodological review |
19 |
| Transcriptomics reveal transgenerational effects in purple sea urchin embryos: Adult acclimation to upwelling conditions alters the response of their progeny to differential pCO(2) levels |
19 |
| The joint evolution of the Myxozoa and their alternate hosts: A cnidarian recipe for success and vast biodiversity |
19 |
| Transitions in sex determination and sex chromosomes across vertebrate species |
18 |
| Spatial population genomics of the brown rat (Rattus norvegicus) in New York City |
18 |
| Why the COI barcode should be the community DNA metabarcode for the metazoa |
18 |
| Quantitative and qualitative assessment of pollen DNA metabarcoding using constructed species mixtures |
18 |
| Genomewide SNP markers breathe new life into phylogeography and species delimitation for the problematic short-necked turtles (Chelidae: Emydura) of eastern Australia |
17 |
| Multiple chromosomal rearrangements in a hybrid zone between Littorina saxatilis ecotypes |
17 |
| Evaluating genomic signatures of the large X-effect during complex speciation |
17 |
| Seascape genomics reveals adaptive divergence in a connected and commercially important mollusc, the greenlip abalone (Haliotis laevigata), along a longitudinal environmental gradient |
17 |
| Host genetic determinants of the gut microbiota of wild mice |
16 |
| The future of parentage analysis: From microsatellites to SNPs and beyond |
16 |
| Macroalgal-bacterial interactions: Role of dimethylsulfoniopropionate in microbial gardening by Ulva (Chlorophyta) |
16 |
| Microbial communities exhibit host species distinguishability and phylosymbiosis along the length of the gastrointestinal tract |
16 |
| Altitudinal variation of the gut microbiota in wild house mice |
16 |
| Two key features influencing community assembly processes at regional scale: Initial state and degree of change in environmental conditions |
16 |
| Rapid genetic adaptation to a novel environment despite a genome-wide reduction in genetic diversity |
15 |
| Large-effect loci affect survival in Tasmanian devils (Sarcophilus harrisii) infected with a transmissible cancer |
15 |
| Oral microbiomes from hunter-gatherers and traditional farmers reveal shifts in commensal balance and pathogen load linked to diet |
15 |
| Response of host-bacterial colonization in shrimp to developmental stage, environment and disease |
15 |
| Chromosomal fusion and life history-associated genomic variation contribute to within-river local adaptation of Atlantic salmon |
14 |
| High-Throughput DNA sequencing of ancient wood |
14 |
| A mirage of cryptic species: Genomics uncover striking mitonuclear discordance in the butterfly Thymelicus sylvestris |
14 |
| Fungal community reveals less dispersal limitation and potentially more connected network than that of bacteria in bamboo forest soils |
14 |
| Burying beetles regulate the microbiome of carcasses and use it to transmit a core microbiota to their offspring |
14 |
| Non-random association patterns in a plant-mycorrhizal fungal network reveal host-symbiont specificity |
14 |
| Early-life telomere length predicts lifespan and lifetime reproductive success in a wild bird |
14 |
| Meta-analysis of chromosome-scale crossover rate variation in eukaryotes and its significance to evolutionary genomics |
14 |
| Introduction: The host-associated microbiome: Pattern, process and function |
13 |
