Results 51 to 60 of about 11,640,365 (320)

Genotyping of pooled microsatellite markers by combinatorial optimization techniques

open access: yesDiscrete Applied Mathematics, 1998
AbstractAn important everyday task for geneticists and molecular biologists is that of isolating and analyzing some particular DNA regions (markers), each drawn from a limited and known set of possible values (alleles). This procedure is called genotyping and is based on DNA amplification and size separation.
LANCIA, Giuseppe, PERLIN M.
openaire   +3 more sources

Genetic variability of blood groups in southern Brazil

open access: yesGenetics and Molecular Biology
We evaluated genetic variability among the blood groups Kell (c.578C > T and c.1790T > C), Kidd (c.838A > G), Duffy (c.125A > G, c.265C > T and c.1-67T > C), Diego (c.2561C > T), MNS (c.143T > C) and Rh (c.676G > C) in Rio Grande do Sul in southern ...
Gabriela Waskow   +6 more
doaj   +1 more source

Comments and Suggestions for Improvement of the Archon Genomics X PRIZE Validation Protocol [PDF]

open access: yes, 2011
This document is a comment on the X PRIZE validation protocol written by Kedes et al. (2011). We propose several modifications which we think will improve the fairness and transparency of the contest while keeping the cost of the validation process ...
Alexander Wait Zaranek   +3 more
core   +2 more sources

Breed traceability of buffalo meat using microsatellite genotyping technique [PDF]

open access: yesJournal of Food Science and Technology, 2017
Although buffalo has emerged as a major meat producing animal in Asia, major research on breed traceability has so far been focused on cattle (beef). This research gap on buffalo breed traceability has impelled development and validation of buffalo breed traceability using a set of eight microsatellite (STR) markers in seven Indian buffalo breeds ...
Bheemashankar H, Kannur   +4 more
openaire   +2 more sources

Methods for Scarless, Selection-Free Generation of Human Cells and Allele-Specific Functional Analysis of Disease-Associated SNPs and Variants of Uncertain Significance. [PDF]

open access: yes, 2017
With the continued emergence of risk loci from Genome-Wide Association studies and variants of uncertain significance identified from patient sequencing, better methods are required to translate these human genetic findings into improvements in public ...
Carvajal-Carmona, Luis G   +4 more
core   +4 more sources

A new biosensor for noninvasive determination of fetal RHD status in maternal blood of RhD negative pregnant women. [PDF]

open access: yesPLoS ONE, 2018
Prenatal detection of the fetal RHD status can be useful in the management of RhD incompatibility to identify fetuses at risk of hemolytic disease. Hemolytic disease causes morbidity and mortality of the fetus in the neonatal period.
Ebru Dündar Yenilmez   +4 more
doaj   +1 more source

A new multi locus variable number of tandem repeat analysis scheme for epidemiological surveillance of Xanthomonas vasicola pv. musacearum, the plant pathogen causing bacterial wilt on banana and enset [PDF]

open access: yes, 2019
Xanthomonas vasicola pv. musacearum (Xvm) which causes Xanthomonas wilt (XW) on banana (Musa accuminata x balbisiana) and enset (Ensete ventricosum), is closely related to the species Xanthomonas vasicola that contains the pathovars vasculorum (Xvv) and ...
Blondin, Laurence   +6 more
core   +4 more sources

[DNA extraction from coagulated human blood for application in genotyping techniques for human leukocyte antigen and immunoglobulin-like receptors].

open access: yesRevista da Sociedade Brasileira de Medicina Tropical, 2009
The objective of this study was to standardize a method for extracting high-quality DNA from samples of coagulated blood. Forty-eight samples of human coagulated blood were used for DNA extraction by means of the EZ-DNA commercial kit (Biological ...
D. Cardozo   +7 more
semanticscholar   +1 more source

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski   +9 more
wiley   +1 more source

Use of genetic markers for the detection of off-types for DUS phenotypic traits in the inbreeding crop, barley [PDF]

open access: yes, 2020
Detection of crop off-types is of interest for multiple uses, including the assessment of uniformity for new plant variety applications during distinctness, uniformity and stability (DUS) testing for the awarding of plant breeders’ rights (PBR). Here,
Cockram, James   +4 more
core   +1 more source

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