Figure 1.
Detection capacity of genomic aberrations with different technologies.1Includes various technologies that may interrogate single nucleotide changes through to the sequence of the entire gene (AS-PCR, fragment analysis, Sanger sequencing, and others). 2Includes gene expression arrays, NanoString, and RT-MLPA assays. 3Most technologies, except FISH, cannot detect subclonal CNAs (<20%) with high confidence. 4Including gene fusions. Ticks indicate good capacity to determine a certain aberration/feature, whereas an inverted red triangle indicates a limited/insufficient detection capacity. AS-PCR, allele-specific oligonucleotide polymerase chain reaction; CNA, copy number aberration; IG, immunoglobulin; indel, insertion-deletion; RT-MLPA, reverse transcriptase multiplex ligation–dependent probe amplification; TR, T-cell receptor locus. Created with BioRender.com.

Detection capacity of genomic aberrations with different technologies.1Includes various technologies that may interrogate single nucleotide changes through to the sequence of the entire gene (AS-PCR, fragment analysis, Sanger sequencing, and others). 2Includes gene expression arrays, NanoString, and RT-MLPA assays. 3Most technologies, except FISH, cannot detect subclonal CNAs (<20%) with high confidence. 4Including gene fusions. Ticks indicate good capacity to determine a certain aberration/feature, whereas an inverted red triangle indicates a limited/insufficient detection capacity. AS-PCR, allele-specific oligonucleotide polymerase chain reaction; CNA, copy number aberration; IG, immunoglobulin; indel, insertion-deletion; RT-MLPA, reverse transcriptase multiplex ligation–dependent probe amplification; TR, T-cell receptor locus. Created with BioRender.com.

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