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3. A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system. Issue 2 (18th February 2019)

4. Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor—A tutorial. Issue 8 (2nd December 2021)

6. DECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research. Issue 6 (21st February 2022)

7. Ensembl 2016. Issue Volume 44:Issue D1(2016) (19th December 2015)

8. Ensembl 2017. Issue Volume 45:Issue D1(2017) (29th November 2016)

9. Ensembl 2018. Issue Volume 46:Issue D1(2018) (16th November 2017)

10. Ensembl 2019. Issue Volume 47:Issue D1(2019) (8th November 2018)