Leveraging multiple genomic data to prioritize disease-causing indels from exome sequencing data

Ítems similars

• Prioritization Of Nonsynonymous Single Nucleotide Variants For Exome Sequencing Studies Via Integrative Learning On Multiple Genomic Data
  per: Wu, Mengmeng, et al.
  Publicat: (2015)
• Global inference of disease-causing single nucleotide variants from exome sequencing data
  per: Wu, Mengmeng, et al.
  Publicat: (2016)
• Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies.
  per: Jiaxin Wu, et al.
  Publicat: (2014-03-01)
• Integrating Multiple Genomic Data to Predict Disease-Causing Nonsynonymous Single Nucleotide Variants in Exome Sequencing Studies
  per: Wu, Jiaxin, et al.
  Publicat: (2014)
• Reducing INDEL calling errors in whole genome and exome sequencing data
  per: Fang, Han, et al.
  Publicat: (2014)