Fine Mapping of the Pond Snail Left-Right Asymmetry (Chirality) Locus Using RAD-Seq and Fibre-FISH

Special features of RAD Sequencing data: implications for genotyping

(2012) John W. Davey et al.   MOLECULAR ECOLOGY

The oyster genome reveals stress adaptation and complexity of shell formation

(2012) Guofan Zhang et al.   NATURE

Insights into bilaterian evolution from three spiralian genomes

(2012) Oleg Simakov et al.   NATURE

INTERNAL SELECTION AGAINST THE EVOLUTION OF LEFT-RIGHT REVERSAL

(2011) Hiroki Utsuno et al.   EVOLUTION

Genome-wide genetic marker discovery and genotyping using next-generation sequencing

(2011) John W. Davey et al.   NATURE REVIEWS GENETICS

Linkage Mapping and Comparative Genomics Using Next-Generation RAD Sequencing of a Non-Model Organism

(2011) Simon W. Baxter et al.   PLoS One

Far from solved: A perspective on what we know about early mechanisms of left-right asymmetry

(2010) Laura N. Vandenberg et al.   DEVELOPMENTAL DYNAMICS

Non-random organization of the Biomphalaria glabrata genome in interphase Bge cells and the spatial repositioning of activated genes in cells co-cultured with Schistosoma mansoni

(2010) Matty Knight et al.   INTERNATIONAL JOURNAL FOR PARASITOLOGY

The effect of coil phenotypes and genotypes on the fecundity and viability ofPartula suturalisandLymnaea stagnalis: implications for the evolution of sinistral snails

(2009) A. DAVISON et al.   JOURNAL OF EVOLUTIONARY BIOLOGY

Chiral blastomere arrangement dictates zygotic left–right asymmetry pathway in snails

(2009) Reiko Kuroda et al.   NATURE

A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

(2008) Richard A. Sturm et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mating behaviour in Lymnaea stagnalis pond snails is a maternally inherited, lateralized trait

(2008) A. Davison et al.   Biology Letters

Velvet: Algorithms for de novo short read assembly using de Bruijn graphs

(2008) D. R. Zerbino et al.   GENOME RESEARCH

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

(2008) Hans Eiberg et al.   HUMAN GENETICS

Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD Markers

(2008) Nathan A. Baird et al.   PLoS One