Case report: identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur
M Fondevila, C Phillips, N Naveran… - Forensic science …, 2008 - Elsevier
Applying two extraction protocols to isolate DNA from a charred femur recovered after a
major forest fire, a range of established and recently developed forensic marker sets that …
major forest fire, a range of established and recently developed forensic marker sets that …
[HTML][HTML] Determination of zygosity in adult Chinese twins using the 450K methylation array versus questionnaire data
B Wang, W Gao, C Yu, W Cao, J Lv, S Wang, Z Pang… - PLoS …, 2015 - journals.plos.org
Previous studies have shown that both single nucleotide polymorphisms (SNPs) and
questionnaires-based method can be used for twin zygosity determination, but few …
questionnaires-based method can be used for twin zygosity determination, but few …
Assessment of the Precision ID Identity Panel kit on challenging forensic samples
C Turchi, C Previderè, C Bini, E Carnevali… - Forensic Science …, 2020 - Elsevier
The performance of the Precision ID Identity Panel (Thermo Fisher Scientific) was assessed
on a set of 87 forensic samples with different levels of degradation for which a reference …
on a set of 87 forensic samples with different levels of degradation for which a reference …
Evolution of single‐nucleotide polymorphism use in forensic genetics
NMM Novroski, JC Cihlar - Wiley Interdisciplinary Reviews …, 2022 - Wiley Online Library
Although short tandem repeats (STRs) are traditionally the marker of choice for traditional
forensic DNA typing applications, single‐nucleotide polymorphisms (SNPs; pronounced …
forensic DNA typing applications, single‐nucleotide polymorphisms (SNPs; pronounced …
[HTML][HTML] Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine
E Chancerel, C Lepoittevin, G Le Provost, YC Lin… - BMC genomics, 2011 - Springer
Abstract Background Single nucleotide polymorphisms (SNPs) are the most abundant
source of genetic variation among individuals of a species. New genotyping technologies …
source of genetic variation among individuals of a species. New genotyping technologies …
Strong intra-and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152
F Cruciani, B Trombetta, C Antonelli, R Pascone… - Forensic Science …, 2011 - Elsevier
More than 2700 unrelated individuals from Europe, northern Africa and western Asia were
analyzed for the marker M269, which defines the Y chromosome haplogroup R1b1b2. A …
analyzed for the marker M269, which defines the Y chromosome haplogroup R1b1b2. A …
Multiplex SNP Genotyping Using SWITCH: Sequence‐Specific Nanoparticle with Interpretative Toehold‐Mediated Sequence Decoding in Hydrogel
W Choi, E Park, S Bae, KH Choi, S Han, KH Son… - Small, 2022 - Wiley Online Library
Single nucleotide polymorphisms (SNPs) that can alter phenotypes of individuals play a
pivotal role in disease development and, more importantly, responses to therapy. However …
pivotal role in disease development and, more importantly, responses to therapy. However …
Identification and Genotyping of Mycobacterium tuberculosis Complex Species by Use of a SNaPshot Minisequencing-Based Assay
C Bouakaze, C Keyser, SJ De Martino… - Journal of clinical …, 2010 - Am Soc Microbiol
The aim of the present study was to investigate the use of the SNaPshot minisequencing
method for the identification of Mycobacterium tuberculosis complex (MTBC) isolates to the …
method for the identification of Mycobacterium tuberculosis complex (MTBC) isolates to the …
[PDF][PDF] A review of gene mutations, conventional testing and novel approaches to cancer screening
N Kulkarni, S Tank, P Korlekar, S Shidhaye… - Int. J. Exp. Res …, 2023 - academia.edu
Cancer is a genetic disease caused due to mutations in the tumor suppressor genes or
oncogenes involved in the cell cycle regulation. It may include mutations that may be …
oncogenes involved in the cell cycle regulation. It may include mutations that may be …
[HTML][HTML] Broadening the applicability of a custom multi-platform panel of microhaplotypes: bio-geographical ancestry inference and expanded reference data
MA De la Puente, J Ruiz-Ramírez… - Frontiers in …, 2020 - frontiersin.org
The development of microhaplotype (MH) panels for massively parallel sequencing (MPS)
platforms is gaining increasing relevance for forensic analysis. Here, we expand the …
platforms is gaining increasing relevance for forensic analysis. Here, we expand the …