Resources
Tumor heterogeneity and evolution
- Single Cell
- Tissue deconvolution
Human Genomics
- Genomic Structural Variation
- Identification of structural variants from the next generation sequencing (NGS) data
- Identification of structural variants from the single molecule (PacBio) sequencing data
- Detection of somatic single nucleotide variants and small indels in NGS cancer genomes
- ClinSeK
- SomaticSniper, additional instructions
- Detection of somatic SNVs and Indels from PCR targeted Sanger sequencing data
Transcriptomics
- Detection of gene fusions from paired end whole-transcriptome RNA-seq data
- Integrative fusion/genomic breakpoint identification from DNA and RNA sequencing data
Functional Genomics
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Research Areas
Find out about the four types of research taking place at MD Anderson.
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