GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arrays

Lignende værker

• MixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cells.
  af: Zongzhi Liu, et al.
  Udgivet: (2010-06-01)
• MixHMM: Inferring Copy Number Variation and Allelic Imbalance Using SNP Arrays and Tumor Samples Mixed with Stromal Cells
  af: Liu, Zongzhi, et al.
  Udgivet: (2010)
• A Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays
  af: Lamy, Philippe, et al.
  Udgivet: (2007)
• QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data
  af: Colella, Stefano, et al.
  Udgivet: (2007)
• Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays
  af: Scharpf, Robert B., et al.
  Udgivet: (2008)