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Fig. 2 | BMC Genomics

Fig. 2

From: Whole genome sequencing facilitates intragenic variant interpretation following modifier screening in C. elegans

Fig. 2

Comparison between Sanger and whole genome sequencing. A. Cost and time investment in using Sanger sequencing to identify strains containing intragenic suppressing variants. B. Cost and time investment in using whole genome sequencing to identify strains containing intragenic suppressing variants. C. Pros, cons, and rate limiting steps for Sanger and whole genome sequencing

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BMC Genomics

ISSN: 1471-2164

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