2018
Nadine AME van der Beek et al.
A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1
European Journal of Human Genetics 2018, vol. 27, issue 3
doi: 10.1038/s41431-018-0250-z
Nadine AME van der Beek et al.
A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1
European Journal of Human Genetics 2018, vol. 27, issue 3
doi: 10.1038/s41431-018-0250-z
Marie-Odile Baudement et al.
High-salt–recovered sequences are associated with the active chromosomal compartment and with large ribonucleoprotein complexes including nuclear bodies
Genome Research 2018, vol. 28, issue 11
doi: 10.1101/gr.237073.118
Philippe Silar et al.
A gene graveyard in the genome of the fungus Podospora comata
Molecular Genetics and Genomics 2018, vol. 294, issue 1
doi: 10.1007/s00438-018-1497-3
Sara Masachis et al.
FASTBAC-Seq: Functional Analysis of Toxin–Antitoxin Systems in Bacteria by Deep Sequencing
Methods in Enzymology 2018
doi: 10.1016/bs.mie.2018.08.033
Wei-Jia Zhang et al.
Complete genome sequence of Shewanella benthica DB21MT-2, an obligate piezophilic bacterium isolated from the deepest Mariana Trench sediment
Marine Genomics 2018, vol. 44
doi: 10.1016/j.margen.2018.09.001
Camille Marchet et al.
De novoclustering of long reads by gene from transcriptomics data
Nucleic Acids Research 2018, vol. 47, issue 1
doi: 10.1093/nar/gky834
L. Allach El Khattabi et al.
Performance of semiconductor sequencing platform for non‐invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting
Ultrasound in Obstetrics & Gynecology 2018, vol. 54, issue 2
doi: 10.1002/uog.20112
L. Allach El Khattabi et al.
Performance of semiconductor sequencing platform for non‐invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting
Ultrasound in Obstetrics & Gynecology 2018, vol. 54, issue 2
doi: 10.1002/uog.20112
Hugo Varet et al.
checkMyIndex: a web-based R/Shiny interface for choosing compatible sequencing indexes
Bioinformatics 2018, vol. 35, issue 5
doi: 10.1093/bioinformatics/bty706