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Table 1 Comparison of various DNA methods (adapted from [135, 237, 245, 247])

From: DNA methods for identification of Chinese medicinal materials

 

SCAR

ARMS

SSR

PCR-RFLP

RP-PCR

ISSR

AFLP

Sequencing

Hybridization

Development cost

medium

medium

high

medium a

low

low

low

medium

medium

Running cost

low

low

medium

medium a

low

low

medium

medium

medium

Polymorphism

low b

low c

high d

low e

medium f

medium f

medium f

medium-low g

only for detection h

Detection of contamination by DNA of the same target species (mixture)

no

no

yes

yes/noi

no

no

no

yes/nok

yes/nok

Detection of contamination by non-target species DNA (mixture)

no

no

no

yes j

no

no

no

yes/nok

yes/nok

Detection of contamination by DNA of the same target species (mixture)

no

no

yes

yes/no i

no

no

no

yes/nok

yes/nok

Detection of contamination by non-target species DNA (mixture)

no

No

no

yesj

No

no

no

yes/nok

yes/nok

Multi-locus/single locus

single locus

single locus

single locus

single locus

multi-loci

multi-loci

multi-loci

single locus

single locus

Level of identification (taxonomic level)

species

species to strain

strain

species to strain

species to strain

species to strain

species to strain

family to strain

genus to subspecies

Quality of DNA required (integrity)

medium

medium

low

medium

high

high

high

medium

medium

Quality of DNA required (purity)

high l

high l

medium

high

high

high

high

high l

high

Prior sequence knowledge requirement (including universal primer sequence)

yes

yes

yes

no

no

no

no

yes

yes

Throughput

low

low

high

low

high

high

high

low

high

Level of skills required

low

low

low-medium

low

low

low

medium

medium

medium

Automation

yes

yes

yes

difficult

yes

yes

yes

yes

difficult

Reliability

high

high

high

high

low

medium

high

high

medium

  1. Development cost: cost for developing standardized reference results for target samples
  2. Running cost: cost for routine testing
  3. Detection of contamination: same target species = samples of the same strain or locality; non-target species = adulterants or substitutes
  4. Multi-locus: simultaneous amplification of multiple regions in the genome in a single PCR
  5. Prior sequence requirement: sequence requirement to design primers for amplification or probes for hybridization
  6. Throughput: number of samples that can be handled within a given period of time
  7. Reliability: giving reproducible and accurate results under the same conditions
  8. a: enzyme dependent
  9. b: band/no band, or size polymorphism
  10. c: band or no band
  11. d: null allele or size polymorphism
  12. e: band number and size polymorphism
  13. f: presence/absence of all the bands in a pattern
  14. g: sequence dependent; nucleotide difference
  15. h: presence or absence of sample DNA
  16. i: restriction enzyme dependent
  17. j: primer dependent
  18. k: sequence dependent
  19. l: crude tolerated