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1. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

2. GA4GH: International policies and standards for data sharing across genomic research and healthcare

3. Twelve years of SAMtools and BCFtools

4. RNA expression differences in prostate tumors and tumor-adjacent stroma between Black and White Americans

5. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

6. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

7. Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseases

8. IFI207, a young and fast‐evolving protein, controls retroviral replication via the STING pathway

9. IFI207, a young and fast-evolving protein, controls retroviral replication via the STING pathway

10. Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci

11. Chromosome assembly of large and complex genomes using multiple references

13. A chromosome-level genome assembly of the Hispid cotton rat (Sigmodon hispidus), a model for human pathogenic virus infections

20. The mutational landscapes of genetic and chemical models of Kras-driven lung cancer

21. Leveraging European infrastructures to access 1 million human genomes by 2022

23. On the abundance of non-cometary HCN on Jupiter

24. A Clinician’s Guide to Next Generation Imaging in Patients With Advanced Prostate Cancer (Prostate Cancer Radiographic Assessments for Detection of Advanced Recurrence [RADAR] III)

27. Assessing the gene space in draft genomes

29. ELIXIR-CONVERGE D7.5 Retrospective assessment of national use-cases, identification of gaps, and recommendations for future Federated EGA roadmap

30. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

32. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans

34. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

36. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

37. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

40. EMBL’s European Bioinformatics Institute (EMBL-EBI) in 2022

42. IFI207, a young and fast-evolving antiviral factor, stabilizes STING

45. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

46. Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022

49. List of contributors

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