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Erratum to: Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens
Genome Medicine volume 8, Article number: 123 (2016)
- The original article was published in Genome Medicine 2016 8:90
It has come to our attention that there is an error in Fig. 3a for this article . The correct version of Fig. 3a can be found below. The red markers now reflect the sequence differences. The text is correct. There was also a row omitted in Additional file 1: Table S1. The revised version can be found below.
Doan T, Wilson MR, Crawford ED, Chow ED, Khan LM, Knopp KA, O’Donovan BD, Xia D, Hacker JK, Stewart JM, Gonzales JA, Archarya NR, DeRisi JL. Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens. Genome Med. 2016;8:106.
List of nucleotide substitutions identified in subject 6’s RV genome. The patient’s RV genome was aligned with the Stuttgart strain (GenBank DQ388280.1). A nucleotide change was considered a substitution only if the change was present in ≥ 4 reads or in 80% of the total reads at that nucleotide position. (PDF 120 kb)
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Doan, T., Wilson, M.R., Crawford, E.D. et al. Erratum to: Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens. Genome Med 8, 123 (2016). https://doi.org/10.1186/s13073-016-0377-x