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Fig. 11 | BMC Genomics

Fig. 11

From: High-specificity detection of rare alleles with Paired-End Low Error Sequencing (PELE-Seq)

Fig. 11

An ilrd-14 SNP at 16 % frequency in the lab-adapted and 0 % in the wild C. remanei. A C > T transition that is completely undetectable in the wild population (0/992 reads) is present at 16 % frequency in the lab-adapted population (159/997 reads). This SNP is located within an intron of a gene predicted to be homologous to the C. elegans gene ilrd-14, which codes for an insulin/EGF receptor L-domain protein. The top panel shows 500 sequencing reads from the ancestral (wild) population; the bottom panel shows 500 sequencing reads from the lab-adapted population. The non-reference SNP at position 22,410,779 of the caeRem3 genome is visible in red

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