ABC Forensic DNA flashcards
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32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Kastle-Meyer test
- Presumptive blood test in which hemoglobin catalyzes oxidation of phenolphthalein by hydrogen peroxide, producing a pink color; plant peroxidases can cause false positives.
- Acid phosphatase test
- Presumptive semen test based on high acid phosphatase activity in seminal fluid; a color change suggests semen, but other body fluids and plant materials can produce false positives.
- Differential extraction
- Extraction method that first lyses epithelial cells, then digests sperm heads with DTT and proteinase K, producing separate non-sperm and sperm DNA fractions.
- Alternate light source
- Screening tool using specific wavelengths and filter goggles to visualize latent biological stains such as semen or saliva; fluorescent areas still require presumptive and confirmatory testing.
- PSA or p30 test
- Confirmatory semen test detecting prostate-specific antigen, a protein from prostate epithelial cells; it is more specific than acid phosphatase but can occur at low levels in other male fluids.
- Sperm microscopy
- Confirmatory semen method in which a stained smear is examined for sperm heads with tails; absence does not exclude azoospermic or vasectomized donors.
- Chelex extraction
- Rapid extraction method using Chelex resin to bind metal ions and protect DNA during boiling; the product is single-stranded DNA suitable for PCR-based typing.
- DTT in extraction
- Dithiothreitol reduces disulfide bonds in sperm protamines, allowing proteinase K to digest sperm heads; it is added after epithelial cells are lysed in differential extraction.
- qPCR quantitation
- Real-time PCR assay that measures human DNA and can estimate male DNA, degradation, and inhibition; it is human-specific and more informative than fluorometry for forensic samples.
- Degradation index
- Ratio of qPCR amplification of a long target to a short target; values above a validated cutoff indicate DNA fragmentation and possible stochastic amplification effects.
- Internal PCR control
- Spike added to qPCR reactions to monitor inhibition; failure or delayed amplification indicates inhibitors that may require dilution or cleanup before STR typing.
- PCR multiplex
- Simultaneous amplification of many STR loci using dye-labeled primers and optimized buffer; multiplex kits include allelic ladders and size standards for typing.
- Allelic ladder
- Reference mixture containing common alleles at each STR locus; it is run with samples to calibrate fragment sizing and assign allele numbers by comparison.
- Internal size standard
- Fluorescently labeled DNA fragments of known sizes added to each capillary electrophoresis injection; they create a size curve converting migration times to base-pair sizes.
- Amelogenin marker
- Sex-typing marker with different X and Y fragment sizes; it usually shows female as X,X and male as X,Y, but a Y deletion can produce a female-like result.
- Stutter peak
- Artifact peak usually one repeat unit shorter than the true allele, caused by slippage during PCR; laboratories apply locus-specific stutter filters before interpretation.
- Pull-up artifact
- Capillary electrophoresis artifact in which a strong signal in one dye channel appears as a smaller peak in another channel; spectral calibration helps prevent it.
- Off-ladder allele
- STR allele whose size does not match a ladder allele within the validated bin; it may be a rare variant and requires confirmation and documentation.
- Analytical threshold
- Peak height or area threshold below which capillary electrophoresis signal is not reliably distinguished from noise; peaks below it are not interpreted as alleles.
- Random match probability
- Probability that a randomly selected unrelated person has the same DNA profile; it is estimated with the product rule using population allele frequencies.
- Likelihood ratio
- Ratio of the probability of the DNA evidence under the prosecution hypothesis to its probability under the defense hypothesis; it quantifies support for one proposition.
- Combined probability of inclusion
- For a diploid mixture, the product across loci of the squared sum of allele frequencies; it estimates the chance a random person would be included as a contributor.
- Allelic drop-out
- Failure to detect an allele that is present because its peak falls below the analytical threshold, often from low template DNA; it can make a heterozygote appear homozygous.
- Allelic drop-in
- Spurious allele peak not derived from the sample, usually seen with low template DNA; replicate amplifications and threshold rules help distinguish it from true alleles.
- Probabilistic genotyping
- Software-based mixture interpretation using peak heights, drop-out probabilities, and statistical models; it outputs a likelihood ratio rather than a simple inclusion or exclusion.
- Theta correction
- Population substructure adjustment using Fst in genotype probability calculations; it accounts for relatedness within populations and generally makes match probability estimates less extreme.
- Reagent blank
- Negative extraction control containing reagents but no sample; it monitors contamination and must produce no DNA profile or remain below validated thresholds.
- Negative amplification control
- PCR reaction with water or buffer instead of DNA; it detects contamination in reagents or workflow and should yield no alleles.
- Proficiency test
- Test sample with known or unknown profile used to evaluate analyst performance; results are reviewed for compliance and may be required for accreditation.
- Internal validation
- Laboratory study before casework demonstrating a method's reliability, sensitivity, specificity, and thresholds under local conditions; results support standard operating procedures.
- Chain of custody
- Chronological documentation of evidence transfer, storage, and handling; it maintains integrity and supports admissibility by showing who had the item and when.
- CODIS
- Combined DNA Index System; FBI-administered network of local, state, and national databases used to search eligible DNA profiles for investigative leads.