ArticleCroatian medical journal2007
Variant alleles, triallelic patterns, and point mutations observed in nuclear short tandem repeat typing of populations in Bosnia and Serbia.
Article in Croatian medical journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
11 citing papers in PubMed, 50 citations in OpenAlex.
- Molecular Characterization and Genetic Significance of a Rare Type-I Triallelic Pattern Involving a 15.3 Microvariant at the D19S433 Locus.International journal of molecular sciences · 2026Article
- Familial Searching utilising the National Forensic DNA Database of South Africa (NFDD-ZA) to aid in the identification of Missing Persons and Unidentified Human Remains.Forensic science international. Synergy · 2025Article
- Identification of skeletal remains in Croatia and Bosnia and Herzegovina, including the homeland war - a 30-year review.Croatian medical journal · 2024Review
- Analysis of data and common mutations encountered during routine parentage testing in Zimbabwe.Scientific reports · 2024Article
- Identification of the Remains of an Adult Using DNA from Their Deciduous Teeth as a Reference Sample.Medicina (Kaunas, Lithuania) · 2023Article
- Improving kinship probability in analysis of ancient skeletons using identity SNPs and MPS technology.International journal of legal medicine · 2023Article
- A case of 46,XX/46,XX chimerism in a phenotypically normal woman.International journal of legal medicine · 2020Article
- Characterization of the extra copy of TPOX locus with tri-allelic pattern.BMC genetics · 2019Article
- Sequence variation of 22 autosomal STR loci detected by next generation sequencing.Forensic science international. Genetics · 2016Article
- Rare sequence variation in the genome flanking a short tandem repeat locus can lead to a question of "nonmaternity".The Journal of molecular diagnostics : JMD · 2010Article
- Template tailoring: Accurate determination of heterozygous alleles using peptide nucleic acid and dideoxyNTP.Electrophoresis · 2010Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
aimTo present a compendium of off-ladder alleles and other genotyping irregularities relating to rare/unexpected population genetic variation, observed in a large short tandem repeat (STR) database from Bosnia and Serbia.
methodsDNA was extracted from blood stain cards relating to reference samples from a population of 32800 individuals from Bosnia and Serbia, and typed using Promega's PowerPlex16 STR kit.
resultsThere were 31 distinct off-ladder alleles were observed in 10 of the 15 STR loci amplified from the PowerPlex16 STR kit. Of these 31, 3 have not been previously reported. Furthermore, 16 instances of triallelic patterns were observed in 9 of the 15 loci. Primer binding site mismatches that affected amplification were observed in two loci, D5S818 and D8S1179.
conclusionInstances of deviations from manufacturer's allelic ladders should be expected and caution taken to properly designate the correct alleles in large DNA databases. Particular care should be taken in kinship matching or paternity cases as incorrect designation of any of these deviations from allelic ladders could lead to false exclusions.
Indexed as
Identifiers
17696304PMC2080559W2182485447What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.