Figure 2
Figure 2. Genomic characterization of myeloid malignancies using Karyogene. Individual AML (n = 62) and MDS (n = 50) samples are represented in columns and genetic mutations in rows. AML samples were unselected whereas MDS samples were pre-selected to harbor chromosomal copy number changes. Mutations are grouped into chromosomal translocations (top), substitutions and indels (middle), CNAs (bottom), and CN-LOH events (bottom row). Clinically relevant CNAs are depicted in separate rows and “other large CNAs” refers to changes affecting regions larger than 3 mbp (described in detail in supplemental Figure 3). The presence of mutations in different contexts is indicated according to the key (bottom left). TF, transcription factor.

Genomic characterization of myeloid malignancies using Karyogene. Individual AML (n = 62) and MDS (n = 50) samples are represented in columns and genetic mutations in rows. AML samples were unselected whereas MDS samples were pre-selected to harbor chromosomal copy number changes. Mutations are grouped into chromosomal translocations (top), substitutions and indels (middle), CNAs (bottom), and CN-LOH events (bottom row). Clinically relevant CNAs are depicted in separate rows and “other large CNAs” refers to changes affecting regions larger than 3 mbp (described in detail in supplemental Figure 3). The presence of mutations in different contexts is indicated according to the key (bottom left). TF, transcription factor.

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