Filoglu, G. and Bulbul, O., Polymorphism in forensic genetics from past to present, in Forensic Biology: Pursuing Justice through the Traces of Nature: II, Istanbul: IUC University Press, 2024, 2nd ed., pp. 45—54.

Google Scholar 

Chintalaphani, S.R., Pineda, S.S., Deveson, I.W., and Kumar, K.R., An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics, Acta Neuropathol. Commun., 2021, vol. 9, no. 1, p. 98. https://doi.org/10.1186/s40478-021-01201-x

Article  PubMed  PubMed Central  Google Scholar 

Tanudisastro, H.A., Deveson, I.W., Dashnow, H., and MacArthur, D.G., Sequencing and characterizing short tandem repeats in the human genome, Nat. Rev. Genet., 2024, vol. 25. no. 7, pp. 460—475. https://doi.org/10.1038/s41576-024-00692-3

Article  CAS  PubMed  Google Scholar 

Kowalczyk, M., Zawadzka, E., Szewczuk, D., et al., Molecular markers used in forensic genetics, Med. Sci. Law, 2018, vol. 58, no. 4, pp. 201—209. https://doi.org/10.1177/0025802418803852

Article  PubMed  Google Scholar 

Butler, J.M., Recent advances in forensic biology and forensic DNA typing: INTERPOL review, Forensic Sci. Int.: Synergy, 2022, vol. 6. https://doi.org/10.1016/j.fsisyn.2022.100311

Keerti, A. and Ninave, S., DNA fingerprinting: use of autosomal short tandem repeats in forensic DNA typing, Cureus, 2022, vol. 14, no. 10. https://doi.org/10.7759/cureus.30210

Machida, M. and Kibayashi, K., Effectiveness of whole genome amplification prior to short tandem repeat analysis for degraded DNA, Forensic. Sci. Int.: Genet., 2020, vol. 49. https://doi.org/10.1016/j.fsigen.2020.102373

Novroski, N.M. and Cihlar, J.C., Evolution of single–nucleotide polymorphism use in forensic genetics, WIREs, Forensic Sci., 2022, vol. 4. https://doi.org/10.1002/wfs2.1459

Gang, A. and Shrivastav, V.K., Single-nucleotide polymorphism, in Handbook of DNA Profiling, Dash, H.R., Shrivastava, P., and Lorente, J.A., Eds., Singapore: Springer-Verlag, 2022, pp. 235—256.

Google Scholar 

Unsal Sapan, T., InDel loci in forensic DNA analysis, in Handbook of DNA Profiling, Dash, H.R., Shrivastava, P., and Lorente, J.A., Eds., Singapore: Springer-Verlag, 2022, pp. 1039—1049.

Google Scholar 

Weber, J.L., David, D., Heil, J., et al., Human diallelic insertion/deletion polymorphisms, Am. J. Hum. Genet., 2002, vol. 71, no. 4, pp. 854—862. https://doi.org/10.1086/342727

Article  PubMed  PubMed Central  Google Scholar 

Pereira, R., Phillips, C., Alves, C., et al., A new multiplex for human identification using insertion/deletion polymorphisms, Electrophoresis, 2009, vol. 30, pp. 3682—3690. https://doi.org/10.1002/elps.200900274

Article  CAS  PubMed  Google Scholar 

Zhang, Q., Wang, X., Cheng, P., et al., Complex kinship analysis with a combination of STRs, SNPs, and indel, Forensic Sci. Int.: Genet., 2022, vol. 61. https://doi.org/10.1016/j.fsigen.2022.102749

Li, J., Lin, L., Jiang, B., et al., An 18 Multi-InDels panel for analysis of highly degraded forensic biological samples, Electrophoresis, 2021, vol. 42, nos. 9—10, pp. 1143—1152. https://doi.org/10.1002/elps.202000245

Article  CAS  PubMed  Google Scholar 

Mahalinga Raja, U., Munuswamy, U., Raghunath, R., et al., Short tandem repeat mutations in paternity analysis, in Handbook of DNA Profiling, Dash, H.R., Shrivastava, P., and Lorente, J.A., Eds., Singapore: Springer-Verlag, 2022, pp. 397—421.

Google Scholar 

Mullaney, J.M., Mills, R.E., Pittard, W.S., and Devine, S.E., Small insertions and deletions (INDELs) in human genomes, Hum. Mol. Genet., 2010, vol. 19, pp. R131—R136. https://doi.org/10.1093/hmg/ddq400

Article  CAS  PubMed  PubMed Central  Google Scholar 

Jin, R., Cui, W., Fang, Y., et al., A novel panel of 43 insertion/deletion loci for human identifications of forensic degraded DNA samples: development and validation, Front. Genet., 2021, vol. 12. https://doi.org/10.3389/fgene.2021.610540

Fang, Y., Liu, Y., Xu, H., and Zhu, B., Performance evaluation of an in-house panel containing 59 autosomal InDels for forensic identification in Chinese Hui and Mongolian groups, Genomics, 2023, vol. 115, no. 1. https://doi.org/10.1016/j.ygeno.2022.110552

Lan, Q., Li, S., Cai, M., et al., A self-developed AIM-InDel panel designed for degraded DNA analysis: forensic application characterization and genetic landscape investigation in the Han Chinese population, Genomics, 2023, vol. 115, no. 3. https://doi.org/10.1016/j.ygeno.2023.110620

Avellaneda, L.L., Johnson, D.T., Gutierrez, R., et al., Development of a novel five-dye panel for human identification insertion/deletion (INDEL) polymorphisms, J. Forensic Sci., 2024, vol. 69, no. 3, pp. 814—824. https://doi.org/10.1111/1556-4029.15475

Article  CAS  PubMed  Google Scholar 

Filoglu, G., Duvenci, A., Tas, S., et al., Development of a multiplex panel with 36 insertion/deletion markers (InDel) for individual identification, Forensic Sci. Med. Pathol., 2024, vol. 20, no. 2, pp. 400–411. https://doi.org/10.1007/s12024-023-00652-z

Azerbaijan—Ethnic Groups, Languages, Religions. https://www.britannica.com/place/Azerbaijan/People. Accessed July 9, 2024.

Nasibov, E., Bulbul, O., Jabrayili, G., et al., Allele frequencies of 15 STR loci in Azerbaijan population, Forensic Sci. Int.: Genet., 2013, vol. 7, pp. e99—e100. https://doi.org/10.1016/j.fsigen.2013.03.004

Article  CAS  PubMed  Google Scholar 

Aliyeva, A., Gellatly, V., Abbasov, M., and Iyengar, A., Population genetic data for 21 autosomal STR loci in the Azerbaijani population using the Globalfiler™ kit, Int. J. Legal. Med., 2021, vol. 135, pp. 1789—1791. https://doi.org/10.1007/s00414-021-02610-2

Article  PubMed  Google Scholar 

Schneider, P.M., Scientific standards for studies in forensic genetics, Forensic Sci. Int., 2007, vol. 165, pp. 238—243. https://doi.org/10.1016/j.forsciint.2006.06.067

Article  CAS  PubMed  Google Scholar 

Sevay, H., Bulbul, O., and Gurkan, C., Statistics in forensic genetics, in Forensic Biology: Pursuing Justice through the Traces of Nature: II, Filoglu, G., and Bulbul, Ö., Eds., Istanbul: IUC University Press, 2024, 2nd ed., pp. 83—94.

Google Scholar 

Butler, J.M., Statistical interpretation overview, in Advanced Topics in Forensic DNA Typing: Interpretation, 2015, pp. 213—237.

Google Scholar 

Chakraborty, R., Sample size requirements for addressing the population genetic issues of forensic use of DNA typing, Hum. Biol., 1992, vol. 64, no. 2, pp. 141—159.

CAS  PubMed  Google Scholar 

Excoffier, L. and Lischer, H., Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. https://onlinelibrary.wiley.com/doi/full/10.1111/j.1755-0998.2010.02-847.x. Accessed May 25, 2022.

Promega Corporation. https://worldwide.promega.com. Accessed October 3, 2021.

Kumar, S. and Tamura, K., Molecular Evolutionary Genetics Analysis Manual: Development, 2009. https://www.megasoftware.net/manual.pdf.

Gürkan, C., Zorba, G.G., and Kanlıada, D., Identification of missing persons using DNA-based methods, in Forensic Biology: Pursuing Justice through the Traces of Nature: II, Filoglu, G. and Bulbul, Ö., Eds., Istanbul: IUC University Press, 2024, 2nd ed., pp. 74—80.

Google Scholar 

Filoğlu, G., Evaluation of population genetics and DNA data, in Forensic Genetics and Genetic Identification, Filoglu, G., Altuncul, H., and Bulbul, Ö., Eds, Ankara: Seckin Yayinevi, 2023, 2nd ed., pp. 353—370.

Google Scholar 

Nwawuba Stanley, U., Mohammed Khadija, A., Bukola, A.T., et al., Forensic DNA profiling: autosomal short tandem repeat as a prominent marker in crime investigation, Malays J. Med. Sci., 2020, vol. 27, no. 4, pp. 22—35. https://doi.org/10.21315/mjms2020.27.4.3

Article  PubMed  PubMed Central  Google Scholar 

Filoğlu, G., Indel polymorphism, in Forensic Genetics and Genetic Identification, Filoglu, G., Altuncul, H., and Bulbul, Ö., Eds., Ankara: Seckin Yayinevi, 2023, pp. 213—233.

Google Scholar 

Li, C., Zhao, S., Zhang, S., et al., Genetic polymorphism of 29 highly informative InDel markers for forensic use in the Chinese Han population, Forensic Sci. Int.: Genet., 2011, vol. 5, pp. 5—8. https://doi.org/10.1016/j.fsigen.2010.03.004

Article  CAS  Google Scholar 

Abreu-Glowacka, M., Pepinski, W., Michalak, E., et al., Population genetic data of 30 insertion-deletion markers in the Polish population, Genes, 2022, vol. 13, no. 10. https://doi.org/10.3390/genes13101683

Pereira, R., Phillips, C., Alves, C., et al., A new multiplex for human identification using insertion/deletion polymorphisms, Electrophoresis, 2009, vol. 30, pp. 3682—3690. https://doi.org/10.1002/elps.200900274

Article  CAS  PubMed  Google Scholar 

LaRue, B.L., Ge, J., King, J.L., and Budowle, B., A validation study of the Qiagen Investigator DIPplex® kit; an INDEL-based assay for human identification, Int. J. Legal Med., 2012, vol. 126, pp. 533—540. https://doi.org/10.1007/s00414-012-0667-9

Article  PubMed  Google Scholar 

Duvenci, A., Bulbul, Ö., and Filoglu, G., Evaluation of population data and forensic parameters of Turkish population on 30 autosomal insertion and deletion polymorphisms, Russ. J. Genet., 2019, vol. 55, pp. 246—252. https://doi.org/10.1134/S1022795419020042

Article  CAS  Google Scholar 

Pimenta, J.R. and Pena, S.D., Efficient human paternity testing with a panel of 40 short insertion-deletion polymorphisms, Genet. Mol. Res., 2010, vol. 9, pp. 601—607. https://doi.org/10.4238/vol9-1gmr838

Article  CAS  PubMed  Google Scholar 

Ensenberger, M.G., Thompson, J., Hill, B., et al., Developmental validation of the PowerPlex® 16 HS System: an improved 16-locus fluorescent STR multiplex, Forensic Sci. Int.: Genet., 2010, vol. 4, pp. 257—264. https://doi.org/10.1016/j.fsigen.2009.10.007

Article  CAS  PubMed  Google Scholar 

Əhali, Azərbaycan Respublikasının Dövlət Statistika Komitəsi, https://www.stat.gov.az/source/demoqraphy/. Accessed October 19, 2021.