| Title | Authors / Editors | Date |
unige:40259 |
De novo finished 2.8 Mbp Staphylococcus aureus genome assembly from 100 bp short and long range paired-end reads |
Hernandez, David; Tewhey, Ryan; Veyrieras, Jean-Baptiste; Farinelli, Laurent Luca Denis; ... Schrenzel, Jacques |
2014 |
unige:32235 |
Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency |
Sosa, Maria Ximena; Sivakumar, I K Ashok; Maragh, Samantha; Veeramachaneni, Vamsi; ... Chakravarti, Aravinda |
2012 |
unige:31209 |
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus |
Anderson, Beverley H; Kasher, Paul R; Mayer, Josephine |
2012 |
unige:25296 |
Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome |
Schaller, André; Hahn, Dagmar; Jackson, Christopher B; Kern, Ilse; ... Nuoffer, Jean-Marc |
2011 |
unige:25010 |
Epidemiology and virulence insights from MRSA and MSSA genome analysis |
Lazarevic, Vladimir; Beaume, Marie-Emilie; Corvaglia, Anna; Hernandez, David; ... Francois, Patrice |
2011 |
unige:34666 |
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice |
Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis |
2011 |
unige:45219 |
A map of human genome variation from population-scale sequencing |
1000 Genomes Project Consortium |
2010 |
unige:18357 |
Contrasting patterns of nuclear and mtDNA diversity in Native American populations |
Yang, Ning Ning; Mazières, Stephane; Bravi, Claudio; Ray, Nicolas; ... Ruiz-Linares, Andrés |
2010 |
unige:8723 |
A cSNP map and database for human chromosome 21 |
Deutsch, Samuel; Iseli, C.; Bucher, P.; Antonarakis, Stylianos; Scott, Hamish Steele |
2001 |