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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Boeva, Valentina, Popova, Tatiana, Bleakley, Kevin, Chiche, Pierre, Cappo, Julie, Schleiermacher, Gudrun, Janoueix-Lerosey, Isabelle, Delattre, Olivier, Barillot, Emmanuel
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2012
Gaiak:
Applications Note
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3268243/
https://ncbi.nlm.nih.gov/pubmed/22155870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr670
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