Copy Number Variation in Forensic Science
Abstract
Full Text:
PDFReferences
Rusk N. Finding copy-number variants. Nature Methods, (2008); 5(11): 917.
Gamazon ER, Nicolae DL, Cox NJ. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci. PLoS genetics, (2011); 7(2): e1001292.
Ju YS, Hong D, Kim S, Park S-S, Kim S, et al. Reference-unbiased copy number variant analysis using CGH microarrays. Nucleic acids research, (2010); 38(20): e190-e190.
CNV-Frequently Ask Questions.
Bianchi L, LiĆ² P. Forensic DNA and bioinformatics. Briefings in bioinformatics, (2007); 8(2): 117-128.
Balaresque P, Parkin EJ, Roewer L, Carvalho-Silva DR, Mitchell RJ, et al. Genomic complexity of the Y-STR DYS19: inversions, deletions and founder lineages carrying duplications. International journal of legal medicine, (2009); 123(1): 15-23.
Butler JM, Decker AE, Kline MC, Vallone PM. Chromosomal duplications along the Y-chromosome and their potential impact on Y-STR interpretation. Journal of forensic sciences, (2005); 50(4): 853.
King T, Bosch E, Adams S, Parkin E, Rosser Z, et al. Inadvertent diagnosis of male infertility through genealogical DNA testing. Journal of medical genetics, (2005); 42(4): 366-368.
Banchs I, Bosch A, Guimera J, Lazaro C, Puig A, et al. New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines. Human mutation, (1994); 3(4): 365-372.
Bosch E, Jobling MA. Duplications of the AZFa region of the human Y chromosome are mediated by homologous recombination between HERVs and are compatible with male fertility. Human molecular genetics, (2003); 12(3): 341-347.
Jobling MA. Copy number variation on the human Y chromosome. Cytogenetic and genome research, (2009); 123(1-4): 253-262.
DOI: http://dx.doi.org/10.62940/als.v1i2.21
Refbacks
- There are currently no refbacks.