Results 11 to 20 of about 83,831 (259)

Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease

open access: yesMolecular Genetics & Genomic Medicine, 2020
Background Polycystic kidney disease (PKD) is an inherited disease that is life‐threatening. Multiple cysts are present in the bilateral kidneys of PKD patients.
Kexian Dong   +16 more
doaj   +1 more source

Incorporating the pedigree information in multi-environment trial analyses for improving common vetch

open access: yesFrontiers in Plant Science, 2023
Common vetch is one of the most profitable forage legumes due to its versatility in end-use which includes grain, hay, green manure, and silage. Furthermore, common vetch is one of the best crops to rotate with cereals as it can increase soil fertility ...
Isabel Munoz Santa   +3 more
doaj   +1 more source

Development of a SNP parentage assignment panel in some North-Eastern Spanish meat sheep breeds

open access: yesSpanish Journal of Agricultural Research, 2021
Aim of study: To validate two existing single nucleotide polymorphism (SNP) panels for parentage assignment in sheep, and develop a cost effective genotyping system to use in some North-Eastern Spanish meat sheep populations for accurate pedigree ...
Jorge H. Calvo   +9 more
doaj   +1 more source

THE STUDY OF EFFECTIVENESS OF AGRICULTURAL RECLAMATION ACTIVITIES IN RICE ROTATION SYSTEM

open access: yesНаучный журнал Российского НИИ проблем мелиорации, 2019
Aim the goal of this research is to identify the efficiency of land grading and provocative irrigation in fallow fields of rice rotation under the conditions of Krasnodar Territory.
N. N. Malysheva, S. V. Kizinyok
doaj   +1 more source

Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family

open access: yesFrontiers in Genetics, 2020
BackgroundLoss-of-function mutations in interferon regulatory factor-6 (IRF6) are responsible for about 70% of cases of Van Der Woude Syndrome (VWS), an autosomal dominant developmental disorder characterized by pits and/or sinuses of the lower lip and ...
Mengqi Zhang   +8 more
doaj   +1 more source

Alternative Ways of Computing the Numerator Relationship Matrix

open access: yesFrontiers in Genetics, 2021
Pedigree relationships between every pair of individuals forms the elements of the additive genetic relationship matrix (A). Calculation of A−1 does not require forming and inverting A, and it is faster and easier than the calculation of A.
Mohammad Ali Nilforooshan   +2 more
doaj   +1 more source

Selective genotyping to implement genomic selection in beef cattle breeding

open access: yesFrontiers in Genetics, 2023
Genomic selection (GS) plays an essential role in livestock genetic improvement programs. In dairy cattle, the method is already a recognized tool to estimate the breeding values of young animals and reduce generation intervals.
Maryam Esrafili Taze Kand Mohammaddiyeh   +4 more
doaj   +1 more source

Comparing Pedigree Graphs [PDF]

open access: yesJournal of Computational Biology, 2012
Pedigree graphs, or family trees, are typically constructed by an expensive process of examining genealogical records to determine which pairs of individuals are parent and child. New methods to automate this process take as input genetic data from a set of extant individuals and reconstruct ancestral individuals.
Bonnie Kirkpatrick   +5 more
openaire   +3 more sources

Compound Uncertainty Quantification and Aggregation for Reliability Assessment in Industrial Maintenance

open access: yesMachines, 2023
The mounting increase in the technological complexity of modern engineering systems requires compound uncertainty quantification, from a quantitative and qualitative perspective.
Alex Grenyer   +3 more
doaj   +1 more source

Establishing Ancestry through Pedigree of a Village with High Prevalence of Hearing-impaired

open access: yesJournal of Indian Speech Language & Hearing Association, 2017
Introduction Population-based surveys into the cause of deafness have consistently shown that a high percentage (50%) of childhood deafness can be attributed to genetic causes.
Sunil Kumar Raina   +3 more
doaj   +1 more source

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