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Fig. 1 | Genome Medicine

Fig. 1

From: Non-canonical antigens are the largest fraction of peptides presented by MHC class I in mismatch repair deficient murine colorectal cancer

Fig. 1

Analysis of mutations targeted in MMR-proficient and MMR-deficient CT26 after injection in immunocompromised and immunocompetent mice. A Experimental workflow employed for the analysis of mutations (SNVs and indels) in WGS data of CT26 Mlh1+/+ and Mlh1-/- samples. Briefly, each CT26 clone was inoculated into NOD-SCID (immunocompromised) and BALB/c (immunocompetent) mice 150 days after genome editing. CT26 MMR-proficient and MMR-deficient tumors underwent WGS at the time of injection and after excision from the mice when tumors reached 1200 mm3 of volume in NOD-SCID mice. In the case of BALB/c mice, the tumors were excised when they reached volumes of 1100 mm3 and 800 mm3 for Mlh1+/+ and Mlh1-/- tumors, respectively. Delta between log fold changes evaluated after injection in immunocompromised and immunocompetent mice in CT26 Mlh1+/+ (B) and CT26 Mlh1-/- (C). Log fold changes analysis of gained and lost alterations was calculated from CT26 Mlh1+/+ and Mlh1-/- pre-injection data, respectively. The alterations were grouped in regions and normalized per Mb before log fold change calculation

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