Skip to main content
Fig. 3 | BMC Bioinformatics

Fig. 3

From: Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management

Fig. 3

Comparison between trimming and MiSeq pipelines in terms of number of identified variants. All variants are shown in panel a, while only single nucleotide variants, insertions and deletions are shown in panel b, c and d, respectively. Dots represent the average on samples belonging to the same panel; error bars represent the 95 % confidence intervals. Solid line represents the linear regression fitting and equation and R2 are displayed in the plot

Back to article page
\