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Fig. 4 | BMC Bioinformatics

Fig. 4

From: Gencore: an efficient tool to generate consensus reads for error suppressing and duplicate removing of NGS data

Fig. 4

Comparison of the alignment files before and after gencore processing In this figure, the position marked by double lines is NM_005228.3(EGFR): c.2369C > T, p.T790 M variant. a visualizes the mapped reads of original alignment file, b visualizes the mapped reads after gencore processing. We can find that the false positive mismatches, which appear randomly in the original alignment file, are corrected by gencore

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