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22 results on '"Claire Lemaitre"'

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1. LEVIATHAN: efficient discovery of large structural variants by leveraging long-range information from Linked-Reads data

2. Genomic architecture of endogenous ichnoviruses reveals distinct evolutionary pathways leading to virus domestication in parasitic wasps

3. Towards a better understanding of the low recall of insertion variants with short-read based variant callers

4. MinYS: mine your symbiont by targeted genome assembly in symbiotic communities

5. SVJedi: genotyping structural variations with long reads

6. DiscoSnp-RAD: de novo detection of small variants for population genomics

7. SimkaMin: fast and resource frugal de novo comparative metagenomics

8. Conserved and specific genomic features of endogenous polydnaviruses revealed by whole genome sequencing of two ichneumonid wasps

9. DiscoSnp++: de novo detection of small variants from raw unassembled read set(s)

10. Critical Assessment of Metagenome Interpretation – a benchmark of computational metagenomics software

11. De Novo NGS Data Compression

12. Footprints of Inversions at Present and Past Pseudoautosomal Boundaries in Human Sex Chromosomes

13. A small trip in the untranquil world of genomes

14. Spodoptera frugiperda (Lepidoptera: Noctuidae) host-plant variants: two host strains or two distinct species?

15. Mapping-free and assembly-free discovery of inversion breakpoints from raw NGS reads

16. Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae

17. Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle

18. Complete Genome Sequence of Mycoplasma putrefaciens Strain 9231, One of the Agents of Contagious Agalactia in Goats

19. Close 3D proximity of evolutionary breakpoints argues for the notion of spatial synteny

20. A novel substitution matrix fitted to the compositional bias in Mollicutes improves the prediction of homologous relationships

21. Cassis: detection of genomic rearrangement breakpoints

22. Analysis of fine-scale mammalian evolutionary breakpoints provides new insight into their relation to genome organisation

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