NGS Analysis of Somatic Mutations in Cancer Genomes
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-41279-5_11
Reference87 articles.
1. Albers CA, Lunter G, MacArthur DG, et al (2011) Dindel: accurate indel calls from short-read data. Genome Res 21:961–973.
2. Andor N, Graham TA, Jansen M, et al (2016) Pan-cancer analysis of the extent and consequences of intratumor heterogeneity. Nat Med 22:105–113.
3. Beerenwinkel N, Schwarz RF, Gerstung M, Markowetz F (2015) Cancer evolution: mathematical models and computational inference. Syst Biol 64:e1–25.
4. Belkadi A, Bolze A, Itan Y, et al (2015) Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants. Proc Natl Acad Sci U S A 112: 5473–5478.
5. Boeva V, Zinovyev A, Bleakley K, et al (2011) Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization. Bioinformatics 27:268–269.
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