Développement Bioinfo

Leandro Lima et al.
Comparative assessment of long-read error correction software applied to Nanopore RNA-sequencing data
Briefings in Bioinformatics 2019
doi: 10.1093/bib/bbz058

Florian Thibord et al.
OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis
RNA 2019, vol. 25, issue 6
doi: 10.1261/rna.069708.118

Alice Fiévet et al.
ART-DeCo: easy tool for detection and characterization of cross-contamination of DNA samples in diagnostic next-generation sequencing analysis
European Journal of Human Genetics 2019, vol. 27, issue 5
doi: 10.1038/s41431-018-0317-x

Eglantine Mathieu-Bégné et al.
De novo transcriptome assembly for Tracheliastes polycolpus, an invasive ectoparasite of freshwater fish in western Europe
Marine Genomics 2019, vol. 46
doi: 10.1016/j.margen.2018.12.001

Caroline Belser et al.
Chromosome-scale assemblies of plant genomes using nanopore long reads and optical maps
Nature Plants 2018, vol. 4, issue 11
doi: 10.1038/s41477-018-0289-4

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

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

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

Gustave Djedatin et al.
DuplicationDetector , a light weight tool for duplication detection using NGS data
Current Plant Biology 2017, vol. 9-10
doi: 10.1016/j.cpb.2017.07.001

Bellenguez C. et al.
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls.
Neurobiol. Aging (2017) Jul. pii: S0197-4580(17)30232-4.
doi: 10.1016/j.neurobiolaging.2017.07.001