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crazyhottommy - cancer genomics
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crazyhottommy

cancer genomics
The University of Texas System • The University of Texas MD Anderson Cancer Center • Houston • United States of America

Skills and expertise

Fields of interest
  • WGS analysis
  • WES analysis
  • BS-seq analysis
Languages
  • Chinese
  • English
Programming languages
  • Python
  • R

Fields of interest

WGS analysis
Identifies copy number variants (CNVs) within targeted next generation…
Displays interactive mining of complex neuroimaging genomics data. Genome…
Allows copy number variation (CNV) detection. iCNV can be applied in whole…
WES analysis
Allows copy number variation (CNV) detection. iCNV can be applied in whole…
Annotates and filtrates variant files. VarAFT allows the comparison of several…
Analyzes structural variants (SVs) and allele-specific copy numbers of genomic…
BS-seq analysis
Annotates and filtrates variant files. VarAFT allows the comparison of several…
Predicts de novo profile generation based on sequence context. SPBuild…
Provides a conversion tool for GFF3 tool to legal EMBL format suitable for…