P765: Leveraging dbSNP for screening rare and novel genetic variants in disease and cancer research

Eitemau Tebyg

• tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine
  gan: Wei, Chih-Hsuan, et al.
  Cyhoeddwyd: (2018)
• dbSNP: the NCBI database of genetic variation
  gan: Sherry, S. T., et al.
  Cyhoeddwyd: (2001)
• Searching NCBI’s dbSNP database
  gan: Bhagwat, Medha
  Cyhoeddwyd: (2010)
• dbSNP: a database of single nucleotide polymorphisms
  gan: Smigielski, Elizabeth M., et al.
  Cyhoeddwyd: (2000)
• Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP
  gan: Zaitlen, Noah A., et al.
  Cyhoeddwyd: (2005)