标签归档:CNV

2015
12-23
CONSERTING: integrating copy-number analysis with structural-variation detection Abstract We developed Copy Number Segmentation by Regression Tree.... Read More >
2015
12-16
Abstract Motivation: Several algorithms exist for detecting copy number variants (CNVs) from human exome sequencing read depth, but previous tools have not been well-suited for large population studi.... Read More >
2015
04-01
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets ABSTRACT Genomic analyses pro.... Read More >
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2015
03-03
A copy number variation map of the human genome Abstract A major contribution to the genome variability among individuals comes from deletions and d.... Read More >
2015
02-26
Spatial and Temporal Heterogeneity in High-Grade Serous Ovarian Cancer: A Phylogenetic Analysis. Abstract BACKGROUND: The major cli.... Read More >
2015
01-20
  Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability. Abstract Genomic instability is.... Read More >
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2015
01-19
Gene expression analysis identifies global gene dosage sensitivity in cancer Many cancer-associated somatic copy number alterations (SCNAs) are known. Currently, one of the challenges is to identify .... Read More >