Table 1.

General advantages, limitations, and clinical applications of comprehensive genomic methods

TechniqueCGFISHCMAOGMTargetedExomeWGSRNA-seq
Viable cells Yes No No No No No No No 
Resolution ∼5 Mb 100-200 kb 20-100 kb 5-50 kb 1 bp 1 bp 1 bp 1 bp 
Coverage Genome Targeted Genome Genome Targeted Exome Genome Genome, Targeted 
Alterations CNV, SV CNV, SV CNV, LOH CNV, SV ← SNV, Indel, CNV, SV, LOH → Gene expression, SV 
Sensitivity (VAF) 5%-10% 1%-5% 30% 5% 2% 5%-10% 10% 5% 
TAT (days)  2-21 1-3 3-14 4-7 5-14 5-14 3-14 5-14 
Cost  $$ $$$ $$-$$$ $$$ $$$$ $$-$$$ 
Worldwide use  High High Low Low Medium Low Low Low 
Used in         
MDS and MDS/MPN D, FU D, FU D, R D, R D, MRD  D, ND  
MPN D, MRD  ND 
AML D, R D, R D, MRD  
ALL D, R D, R D, R 
TechniqueCGFISHCMAOGMTargetedExomeWGSRNA-seq
Viable cells Yes No No No No No No No 
Resolution ∼5 Mb 100-200 kb 20-100 kb 5-50 kb 1 bp 1 bp 1 bp 1 bp 
Coverage Genome Targeted Genome Genome Targeted Exome Genome Genome, Targeted 
Alterations CNV, SV CNV, SV CNV, LOH CNV, SV ← SNV, Indel, CNV, SV, LOH → Gene expression, SV 
Sensitivity (VAF) 5%-10% 1%-5% 30% 5% 2% 5%-10% 10% 5% 
TAT (days)  2-21 1-3 3-14 4-7 5-14 5-14 3-14 5-14 
Cost  $$ $$$ $$-$$$ $$$ $$$$ $$-$$$ 
Worldwide use  High High Low Low Medium Low Low Low 
Used in         
MDS and MDS/MPN D, FU D, FU D, R D, R D, MRD  D, ND  
MPN D, MRD  ND 
AML D, R D, R D, MRD  
ALL D, R D, R D, R 

ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; CG, cytogenetics; CMA, chromosomal microarray; CNV, copy number variations; D, diagnosis; ES, exome sequencing; FISH, fluorescence in situ hybridization; FU, follow-up; Indel, small insertion/deletions; LOH, loss-of-heterozygosity; MPN, myeloproliferative neoplasm; ND, not done; OGM, optical genome mapping; R, relapse; SNV, single nucleotide variant; SV, structural variant; TAT, turnaround time.

TATs, cost, and use approximated. Actual TATs, cost, and use vary significantly by region and laboratory.

When used in conjunction with high coverage sequencing and error correction methods for increased sensitivity/specificity for low-abundance mutations.

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