Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

qPCR and mtDNA SNP analysis of experimentally degraded hair samples and its application in forensic casework.

International journal of legal medicine - 1 Jul 2010

Köhnemann Stephan, Pennekamp Petra, Schmidt Peter Fritz, Pfeiffer Heidi

Abstract excerpt

A mitochondrial DNA (mtDNA) quantification PCR (qPCR) method was developed and applied in a study with experimentally degraded hair samples (first study) and in a criminal case (second study). In the first study, the amount of detectable mtDNA decreased drastically after an incubation time of 1 month on a moist tissue in a heating cabin at 37 degrees C. In the second study, when the qPCR assay showed positive...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA Fingerprinting
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hair Color

Share to Microscopy, Electron, Scanning

Share to Polymerase Chain Reaction

Share to Polymorphism, Single Nucleotide

Share to Specimen Handling

Source

Identifiers

PMID: 20499247
DOI: 10.1007/s00414-010-0466-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

qPCR and mtDNA SNP analysis of experimentally degraded hair samples and its application in forensic casework.PMID 20499247Read ↗

Application of mtDNA SNP analysis in forensic casework.Semantic proximity Read ↗

Development and validation of a D-loop mtDNA SNP assay for the screening of specimens in forensic casework.Semantic proximity Read ↗

Half-volume validation of the NGM Detect™ PCR Amplification Kit and its application on degraded casework samples.Semantic proximity Read ↗

A point-of-care platform for hair loss-related single nucleotide polymorphism genotyping.Semantic proximity Read ↗

Concurrent genotyping of mitochondrial DNA and nuclear DNA in rootless hair shafts and blood samples for enhanced analysis.Semantic proximity Read ↗

A human identification system for hair shaft using RNA polymorphism.Semantic proximity Read ↗

Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis.Semantic proximity Read ↗

Hairy matters: MtDNA quantity and sequence variation along and among human head hairs.Semantic proximity Read ↗

Direct detection of single nucleotide polymorphism (SNP) by the TaqMan PCR assay using dried saliva on water-soluble paper and hair-roots, without DNA extraction.Semantic proximity Read ↗

Damage patterns observed in mtDNA control region MPS data for a range of template concentrations and when using different amplification approaches.Semantic proximity Read ↗

[Application of multiplex amplification of mitochondrial DNA single nucleotide polymorphism in the detection of complex forensic samples].Semantic proximity Read ↗

Routine Mitogenome MPS Analysis from 1 and 5 mm of Rootless Human HairSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.