GeneMarker® HID: A Reliable Software Tool for the Analysis of Forensic STR Data

Journal of Forensic Sciences

Volumn 56, Issue 1, 2011, Pages 29-35

  Holland, Mitchell M ^a   Parson, Walther ^b  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

^b INNSBRUCK MEDICAL UNIVERSITY   (Austria)

Author keywords

Forensic science; High throughput laboratory analysis; Short tandem repeat analysis software

Indexed keywords

ARTICLE; COMPUTER PROGRAM; DNA FINGERPRINTING; EVALUATION; HUMAN; REPRODUCIBILITY; TANDEM REPEAT;

DNA FINGERPRINTING; HUMANS; REPRODUCIBILITY OF RESULTS; SOFTWARE; TANDEM REPEAT SEQUENCES;

EID: 78650734587     PISSN: 00221198     EISSN: 15564029     Source Type: Journal    
DOI: 10.1111/j.1556-4029.2010.01565.x     Document Type: Article

References (14)

1. White TJ, Arnheim N, Erlich HA. The polymerase chain reaction. Trends Genet 1989;5(6):185-9.
2. Gill P, Kimpton CP, Urquhart A, Oldroyd N, Millican ES, Watson SK, et al. Automated short tandem repeat (STR) analysis in forensic casework-a strategy for the future. Electrophoresis 1995;16(9):1543-52.
3. Nagy M, Otremba P, Kruger C, Bergner-Greiner S, Andres P, Henske B, et al. Optimization and validation of a fully automated silica-coated magnetic beads purification technology in forensics. Forensic Sci Int 2005;152(1):13-22.
4. Fregeau CJ, Lett CM, Elliot J, Yensen C, Fourney RM. Automated processing of forensic casework samples using robotic workstations equipped with nondisposable tips: contamination prevention. J Forensic Sci 2008;53(3):632-51.
5. Oberacher H, Pitterl F, Huber G, Niederstatter H, Steinlechner M, Parson W. Increased forensic efficiency of DNA fingerprints through simultaneous resolution of length and nucleotide variability by high-performance mass spectrometry. Hum Mutat 2008;29(3):427-32.
6. Holland BR, Clarke AC, Meudt HM. Optimizing automated AFLP scoring parameters to improve phylogenetic resolution. Syst Biol 2008;7(3):347-66.
7. Kadash K, Kozlowski BE, Biega LA, Duceman BW. Validation study of the TrueAllele automated data review system. J Forensic Sci 2004;49(4):660-7.
8. Milunsky JM, Maher TA, Ito M, Milunsky A. The value of MLPA in Waardenburg Syndrome. Genet Test 2007;11(2):179-82.
9. Miller NJ, Ciosi M, Sappington TW, Ratcliffe ST, Spencer JL, Guillemaud T. Genome scan of Diabrotica virgifera virgifera for genetic variation associated with crop rotation tolerance. J Appl Entomol 2007;131(6):378-85.
10. Funke BH, Brown AC, Ramoni MF, Regan ME, Baglieri C, Finn CT, et al. A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions. Genetic Testing 2007;11(1):91-100.
11. del Gaudio D, Fang P, Scaglia F, Ward P, Craigen WJ, Glaze DG, et al. Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med 2006;8(12):789-92.
12. Mitchell MG, Tabarini D, Ziman M. Loss of heterozygosity analysis at selected single nucleotide polymorphism sites in the intronic regions of PAX7 via in silico biology and microsatelite analysis. J Am Sci 2006;2:4.
13. Curtin CD, Bellon JR, Henschke PA, Godden PW, de Barros Lopes MA. Genetic diversity of Dekkera bruxellensis yeasts isolated from Australian wineries. FEMS Yeast Res 2007;7(3):471-81.
14. Grubwieser P, Mühlmann R, Berger B, Niederstätter H, Pavlic M, Parson W. A new "miniSTR-multiplex" displaying reduced amplicon lengths for the analysis of degraded DNA. Int J Legal Med 2006;120:115-20.