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Erratum to: Extensive next-generation sequencing analysis in chronic lymphocytic leukemia at diagnosis: clinical and biological correlations
Journal of Hematology & Oncology volume 9, Article number: 103 (2016)
The Original Article was published on 15 September 2016
Erratum
n.b. The error described below was mistakenly carried forward by the production team handling this article, and thus was not the fault of the authors.
The original version of this article [1] had a duplication of Fig. 1 in place of where Fig. 2 should have been, resulting in two displays of Fig. 1 and the absence of Fig. 2.
The article has now been updated to remove the duplicate of Fig. 1 and to insert the correct Fig. 2 into its appropriate place.
The two figures in question can be seen below.
Gene mutations and correlation with genomic features: circos diagrams illustrating pairwise co-occurrence of gene mutations with IGHV status, FISH results, and complex karyotype
TTFT according to number of mutations by NGS analysis (p < 0.001)
References
Rigolin GM, Saccenti E, Bassi C, Lupini L, Quaglia FM, Cavallari M, Martinelli S, Formigaro L, Lista E, Bardi MA, Volta E, Tammiso E, Melandri A, Urso A, Cavazzini F, Negrini M, Cuneo A. Extensive next-generation sequencing analysis in chronic lymphocytic leukemia at diagnosis: clinical and biological correlations. J Hematol Oncol. 2016;9:88. doi:10.1186/s13045-016-0320-z.
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The online version of the original article can be found under doi:10.1186/s13045-016-0320-z.
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Rigolin, G.M., Saccenti, E., Bassi, C. et al. Erratum to: Extensive next-generation sequencing analysis in chronic lymphocytic leukemia at diagnosis: clinical and biological correlations. J Hematol Oncol 9, 103 (2016). https://0-doi-org.brum.beds.ac.uk/10.1186/s13045-016-0331-9
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DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s13045-016-0331-9