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Genetic polymorphisms and phylogenetic analysis of the Gujarat population via 17 Y chromosomal STR systems
Analysis of Y‑STRs provides valuable information in forensic casework as well as in population studies. In order to observe the genetic polymorphism...
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Development and validation of a novel 133-plex forensic STR panel (52 STRs and 81 Y-STRs) using single-end 400 bp massive parallel sequencing
Short tandem repeats (STRs) are the preferred genetic markers in forensic DNA analysis, routinely measured by capillary electrophoresis (CE) method...
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Development of an NGS panel containing 42 autosomal STR loci and the evaluation focusing on secondary kinship analysis
High-throughput next-generation sequencing (NGS) is a feasible technique to detect considerably more markers and simultaneously obtain length and...
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Developmental validation of the STRscan-17LC kit: a 6 Dye STR kit enhanced stability and ability to detect degraded samples
Genoty** of short tandem repeat (STR) markers is the basic method of forensic science. Enhanced technologies are needed to meet the requirements of...
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Validation of the Microreader 40Y ID System: a Y-STR multiplex for casework and database samples
Y-chromosome-specific short tandem repeat loci (Y-STRs) are commonly analysed in forensic science for paternity testing, familial searches, and, in...
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Genetic inconsistency at the D6S1043 locus caused by microdeletion at 6q15
In the practice of parentage testing, short tandem repeat (STR) genetic inconsistencies occasionally occur and are usually treated as genetic...
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Genetic polymorphisms of new 22 autosomal STR loci in the Mongolian ethnic group
The Microreader™ 23SP ID System is a novel STR kit, but there are no Mongolian data related to this kit. In this study, allelic frequencies and...
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Large fragment Sanger sequencing identifies the newly encountered variant that caused null alleles in parentage testing
Short tandem repeat (STR) is regarded as a crucial tool for personal identification as well as parentage testing. Thus, genoty** errors of STRs...
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Establishment of a co-analysis system for personal identification and body fluid identification: a preliminary report
Analysis of genetic markers can provide clues for case investigation. Short tandem repeat (STR) detection and analysis are widely used for both...
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Forensic nanopore sequencing of STRs and SNPs using Verogen’s ForenSeq DNA Signature Prep Kit and MinION
The MinION nanopore sequencing device (Oxford Nanopore Technologies, Oxford, UK) is the smallest commercially available sequencer and can be used...
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Challenges in the recovery of the genetic data from human remains found on the Western Balkan migration route
Traditional DNA-based identification of human remains relies on the system of matching STR profile of the deceased with the family references or...
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A quantifiler™ trio-based HRM screening assay for the accurate prediction of single source versus mixed biological samples
At present, the forensic DNA workflow is not capable of providing information about the contributor status (single source vs. multiple contributors)...
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Detecting genetic hypermutability of gastrointestinal tumor by using a forensic STR kit
Growing evidence suggests that somatic hypermutational status and programmed cell death-1 overexpression are potential predictive biomarkers...
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Enhanced mixture interpretation with macrohaplotypes based on long-read DNA sequencing
Deconvoluting mixture samples is one of the most challenging problems confronting DNA forensic laboratories. Efforts have been made to provide...
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Multiplex STR panel for assessment of chimerism following hematopoietic stem cell transplantation (HSCT)
Short tandem repeat (STR) analysis is used in chimerism monitoring after allogeneic hematopoietic stem cell transplantation (HSCT) for patients with...
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Meta-analysis of genome-wide association studies of hoarding symptoms in 27,651 individuals
Hoarding Disorder (HD) is a mental disorder characterized by persistent difficulties discarding or parting with possessions, often resulting in...
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Validation of the Applied Biosystems RapidHIT ID instrument and ACE GlobalFiler Express sample cartridge
Rapid DNA platforms are fully automated systems capable of processing DNA from biological samples and interpreting the results in approximately...
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Developmental validation of the MGIEasy Signature Identification Library Prep Kit, an all-in-one multiplex system for forensic applications
Analyzing genetic markers in nuclear and mitochondrial genomes is helpful in various forensic applications, such as individual identifications and...
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Forensic characterization of 124 SNPs in the central Indian population using precision ID Identity Panel through next-generation sequencing
With the advent of next-generation sequencing technology, SNP markers are being explored as a useful alternative to conventional capillary...
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Preclinical efficacy of targeting epigenetic mechanisms in AML with 3q26 lesions and EVI1 overexpression
AML with chromosomal alterations involving 3q26 overexpresses the transcription factor (TF) EVI1, associated with therapy refractoriness and inferior...
