ClinVar: improving access to variant interpretations and supporting evidence https://t.co/kt04GIrhFQ
RT @NCBI: In the 2020 NAR database issue, we discuss updates to ClinVar https://t.co/DgQAqzWRmT
In the 2020 NAR database issue, we discuss updates to ClinVar https://t.co/DgQAqzWRmT
ClinVar: improving access to variant interpretations and supporting evidence https://t.co/yufIQ3R9kG
RT @NCBI: In the 2018 NAR database issue, we discuss updates to ClinVar, including improved variant call files, a new XML report, and accep…
In the 2018 NAR database issue, we discuss updates to ClinVar, including improved variant call files, a new XML report, and accepting a new type of submissions: https://t.co/DgQAqzWRmT
RT @LeucineRichBio: ClinVar: improving access to variant interpretations and supporting evidence https://t.co/yt5NXTcdnU
ClinVar: improving access to variant interpretations and supporting evidence https://t.co/yt5NXTcdnU
RT @TheFirstNuomics: ClinVar: improving access to variant interpretations and supporting evidence | Nucleic Acids Research | Oxford Academi…
RT @TheFirstNuomics: ClinVar: improving access to variant interpretations and supporting evidence | Nucleic Acids Research | Oxford Academi…
RT @TheFirstNuomics: ClinVar: improving access to variant interpretations and supporting evidence | Nucleic Acids Research | Oxford Academi…
RT @TheFirstNuomics: ClinVar: improving access to variant interpretations and supporting evidence | Nucleic Acids Research | Oxford Academi…
ClinVar: improving access to variant interpretations and supporting evidence | Nucleic Acids Research | Oxford Academic https://t.co/6gYt8nk44u