Search "+SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data"
Pages related to:
but not related to:
Positive matches
- 0.056 + - PatternCNV
- 0.056 + - SegSeq
- 0.056 + - Control-FREEC
- 0.056 + - Copy-number variation
- 0.056 + - SNP array
- 0.056 + - NGS
- 0.056 + - CNV-seq
- 0.056 + - Data analysis
- 0.056 + - saasCNV
- 0.056 + - Aneuploidy
- 0.056 + - 2015
- 0.056 + - November 19
- 0.056 + - PLOS Computational Biology
- 0.056 + - R
- 0.056 + - WGS
- 0.056 + - CNV calling from NGS data
- 0.056 + - ExomeCNV
- 0.056 + - Exome sequencing
- 0.025 + - bioRxiv
- 0.025 + - May 9