Skip to main content
Fig. 3 | GigaScience

Fig. 3

From: Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies

Fig. 3

Overlap of called variations between libraries. Single nucleotide variants (SNVs) numbering 3.24 million were called in the STD library, and over 2.85 million in each of the LFR libraries. The overlap between each library was compared and plotted. The standard library (black), and LFR libraries 1 (blue) and 2 (green) are highly overlapping, demonstrating that the majority of the variant calls are highly reproducible between separately processed sequencing libraries

Back to article page