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1. Enterosignatures define common bacterial guilds in the human gut microbiome

2. Galaxy Training: A Powerful Framework for Teaching!

3. Four functional profiles for fibre and mucin metabolism in the human gut microbiome

4. Democratizing knowledge representation with BioCypher

5. From bag-of-genes to bag-of-genomes: metabolic modelling of communities in the era of metagenome-assembled genomes

6. Strainberry: automated strain separation in low-complexity metagenomes using long reads

7. Describing variability in pig genes involved in coronavirus infections for a One Health perspective in conservation of animal genetic resources

8. Disentangling the complexity of low complexity proteins

9. Swarm v3: towards tera-scale amplicon clustering

10. Metagenomic assessment of the global distribution of bacteria and fungi

11. Metage2Metabo, microbiota-scale metabolic complementarity for the identification of key species

12. A single-cell RNA-sequencing training and analysis suite using the Galaxy framework

13. Assessment of genetically modified maize MZIR098 for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA‐GMO‐DE‐2017‐142)

14. Whole-genome sequencing of European autochthonous and commercial pig breeds allows the detection of signatures of selection for adaptation of genetic resources to different breeding and production systems

15. Assessment of genetically modified oilseed rape GT73 for renewal authorisation under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-002) EFSA Panel on Genetically Modified Organisms (GMO), Panel members: Scientific Opinion

16. Genome-wide detection of copy number variants in European autochthonous and commercial pig breeds by whole-genome sequencing of DNA pools identified breed-characterising copy number states

17. Assessment of genetically modified soybean MON 87705 3 MON 87708 3 MON 89788, for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2015-126)

18. Assessment of genetically modified maize MON 88017 for renewal authorisation under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-014) EFSA Panel on Genetically Modified Organisms (GMO), Panel members: Scientific Opinion

19. Assessment of genetically modified soybean SYHT0H2 for food and feed uses, import and processing, under Regulation (EC) No 1829/2003 (application EFSA-GMO-DE- 2012-111)

20. Current status of the multinational Arabidopsis community

21. Wheat chromatin architecture is organized in genome territories and transcription factories

22. Unraveling the subtleties of β-(1→3)-glucan phosphorylase specificity in the GH94, GH149, and GH161 glycoside hydrolase families

23. Assessment of genetically modified maize MON 89034 for renewal authorisation under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-015) EFSA Panel on Genetically Modified Organisms (GMO), Panel members

24. Statement complementing the EFSA Scientific Opinion on application (EFSA-GMO-UK-2006-34) for authorisation of food and feed containing, consisting of and produced from genetically modified maize 3272 EFSA Panel on Genetically Modified Organisms (GMO)

25. EFSA Panel on Genetically Modified Organisms (GMO)

26. Assessment of genetically modified soybean MON 87708 × MON 89788 × A5547-127, for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2016-135)

27. Assessment of genetically modified maize MIR604 for renewal authorisation under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-013) EFSA Panel on Genetically Modified Organisms (GMO), Panel members

28. Scientific Opinion

29. Assessment of genetically modified maize MON 87427 3 MON 87460 3 MON 89034 3 MIR162 3 NK603 and subcombinations, for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2016-134): Scientific Opinion

30. Identification of Euglena gracilis β-1,3-glucan phosphorylase and establishment of a new glycoside hydrolase (GH) family GH149

31. Assessment of genetically modified soybean MON 89788 for renewal of authorisation under Regulation (EC) No 1829/2003 (application EFSA-GMO-RX-011) EFSA Panel on Genetically Modified Organisms (GMO), Panel members

32. Preliminary insights into the genetics of bank vole tolerance to Puumala hantavirus in Sweden : XXXX

33. The ash dieback invasion of Europe was founded by two genetically divergent individuals

34. ReGaTE: Registration of Galaxy Tools in Elixir

35. Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species

36. Erratum to: Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species

37. Developing data interoperability using standards : a wheat community use case

38. Community-Driven Data Analysis Training for Biology

39. Charge-density analysis using multipolar atom and spherical charge models: 2-methyl-1,3-cyclopentanedione, a compound displaying a resonance-assisted hydrogen bond

40. Dispersal strategies shape persistence and evolution of human gut bacteria

41. From synthetic communities to synthetic ecosystems: exploring causalities in plant-microbe-environment interactions.

42. CTLA-4 expressing innate lymphoid cells modulate mucosal homeostasis in a microbiota dependent manner.

43. Community standards and future opportunities for synthetic communities in plant-microbiota research.

44. Building pangenome graphs.

45. A history-dependent integrase recorder of plant gene expression with single-cell resolution.

46. mulea: An R package for enrichment analysis using multiple ontologies and empirical false discovery rate.

47. Author Correction: The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics.

48. Socially plastic responses in females are robust to evolutionary manipulations of adult sex ratio and adult nutrition.

49. Single-cell RNA sequencing offers opportunities to explore the depth of physiology, adaptation, and biochemistry in non-model organisms exposed to pollution.

50. Genomics-informed captive breeding can reduce inbreeding depression and the genetic load in zoo populations.

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