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Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data
Summary: More and more cancer studies use next-generation sequencing (NGS) data to detect various types of genomic variation. However, even when researchers have such data at hand, single-nucleotide polymorphism arrays have been considered necessary to assess copy number alterations and especially l...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268243/ https://www.ncbi.nlm.nih.gov/pubmed/22155870 http://dx.doi.org/10.1093/bioinformatics/btr670 |