keyword
https://read.qxmd.com/read/35983410/genome-wide-association-and-genomic-prediction-of-growth-traits-in-the-european-flat-oyster-ostrea-edulis
#21
JOURNAL ARTICLE
Carolina Peñaloza, Agustin Barria, Athina Papadopoulou, Chantelle Hooper, Joanne Preston, Matthew Green, Luke Helmer, Jacob Kean-Hammerson, Jennifer C Nascimento-Schulze, Diana Minardi, Manu Kumar Gundappa, Daniel J Macqueen, John Hamilton, Ross D Houston, Tim P Bean
The European flat oyster ( Ostrea edulis ) is a bivalve mollusc that was once widely distributed across Europe and represented an important food resource for humans for centuries. Populations of O. edulis experienced a severe decline across their biogeographic range mainly due to overexploitation and disease outbreaks. To restore the economic and ecological benefits of European flat oyster populations, extensive protection and restoration efforts are in place within Europe. In line with the increasing interest in supporting restoration and oyster farming through the breeding of stocks with enhanced performance, the present study aimed to evaluate the potential of genomic selection for improving growth traits in a European flat oyster population obtained from successive mass-spawning events...
2022: Frontiers in Genetics
https://read.qxmd.com/read/35980984/fgfrl1-and-fgf-genes-are-associated-with-height-hypertension-and-osteoporosis
#22
JOURNAL ARTICLE
Hye-Won Cho, Hyun-Seok Jin, Yong-Bin Eom
Hypertension and osteoporosis are two major disorders, which interact with each other. Specific genetic signals involving the fibroblast growth factor receptor-like 1 (FGFRL1) gene are related to high blood pressure and bone growth in giraffes. FGFRL1 is associated with cardiovascular system and bone formation. We performed an association study to investigate the role of FGFRL1 in hypertension, osteoporosis, and height determination in humans. In addition, we identified three kinds of phenotypes in fibroblast growth factor (FGF) genes and examined their association with the FGFRL1 gene...
2022: PloS One
https://read.qxmd.com/read/35953943/-kat2b-gene-polymorphisms-are-associated-with-body-measure-traits-in-four-chinese-cattle-breeds
#23
JOURNAL ARTICLE
Xiaoding Lin, Bo Li, Yuhan Chen, Hong Chen, Mei Liu
Identifying molecular markers related to growth characteristics or meat quality is significant for improving beef cattle breeds. K(lysine) acetyltransferase 2B ( KAT2B ) is a transcriptional co-activator regulating the acetylation modification of histones, which may be involved in the development and metabolism of muscle and adipose. However, investigations of KAT2B genetic variations in Chinese native cattle are still limited. This study aimed to identify crucial single nucleotide polymorphisms (SNPs) influencing the body measurements of Chinese native cattle...
August 1, 2022: Animals: An Open Access Journal From MDPI
https://read.qxmd.com/read/35681932/snp-genotyping-characterizes-the-genome-composition-of-the-new-baisary-fat-tailed-sheep-breed
#24
JOURNAL ARTICLE
Narzhan Zhumadillayev, Kairat Dossybayev, Aigerim Khamzina, Tilek Kapasuly, Zhangylsyn Khamzina, Nurlan Tlevlesov
Lamb meat has become increasingly popular in several nations during the last few decades, especially in Kazakhstan. Due to the rising demand for lamb meat, our sheep breeders developed a new fat-tailed sheep and named the breed Baisary. Animals of the Baisary breed are characterized by a large physique, strong constitution, stretched body, deep and wide chest, medium or large-sized fat tail, long legs (height at the withers of adult rams 85-100 cm, sheep 75-90 cm), long lanceolate ears and strong hooves. Lambs of the Baisary breed surpass their peers of the original parent breeds by 15-20% in live weight at the weaning period...
June 6, 2022: Animals: An Open Access Journal From MDPI
https://read.qxmd.com/read/35427851/forensic-dna-phenotyping-inferring-phenotypic-traits-from-crime-scene-dna
#25
REVIEW
Prashita Dabas, Sonal Jain, Himanshu Khajuria, Biswa Prakash Nayak
INTRODUCTION: Forensic DNA Phenotyping (FDP) has provided better understanding of various phenotypic features (e.g., height, skin colour, eye colour, structure and shape of scalp hair, baldness, facial features etc.) and associated genetic variations. The current study was designed to investigate the genetic variants and their potential contribution towards accurate phenotype prediction systems. Short Tandem Repeat (STR) based DNA typing method can be uninformative or with little potential to solve a crime in absence of suspect DNA profile in the database...
May 2022: Journal of Forensic and Legal Medicine
https://read.qxmd.com/read/35371186/high-resolution-genome-wide-association-studies-reveal-rich-genetic-architectures-of-grain-zinc-and-iron-in-common-wheat-triticum-aestivum-l
#26
JOURNAL ARTICLE
Jingyang Tong, Cong Zhao, Mengjing Sun, Luping Fu, Jie Song, Dan Liu, Yelun Zhang, Jianmin Zheng, Zongjun Pu, Lianzheng Liu, Awais Rasheed, Ming Li, Xianchun Xia, Zhonghu He, Yuanfeng Hao
Biofortification is a sustainable strategy to alleviate micronutrient deficiency in humans. It is necessary to improve grain zinc (GZnC) and iron concentrations (GFeC) in wheat based on genetic knowledge. However, the precise dissection of the genetic architecture underlying GZnC and GFeC remains challenging. In this study, high-resolution genome-wide association studies were conducted for GZnC and GFeC by three different models using 166 wheat cultivars and 373,106 polymorphic markers from the wheat 660K and 90K single nucleotide polymorphism (SNP) arrays...
2022: Frontiers in Plant Science
https://read.qxmd.com/read/34949768/a-summary-statistics-based-approach-to-examine-the-role-of-serotonin-transporter-promoter-tandem-repeat-polymorphism-in-psychiatric-phenotypes
#27
JOURNAL ARTICLE
Arunabha Majumdar, Preksha Patel, Bogdan Pasaniuc, Roel A Ophoff
In genetic studies of psychiatric disorders in the pre-genome-wide association study (GWAS) era, one of the most commonly studied loci is the serotonin transporter (SLC6A4) promoter polymorphism, a 43-base-pair insertion/deletion polymorphism in the promoter region (5-HTTLPR). The genetic association signals between 5-HTTLPR and psychiatric phenotypes, however, have been inconsistent across many studies. Since the polymorphism cannot be tested via available SNP arrays, we had previously proposed an efficient machine learning algorithm to predict the genotypes of 5-HTTLPR based on the genotypes of eight nearby SNPs, which requires access to individual-level genotype and phenotype data...
May 2022: European Journal of Human Genetics: EJHG
https://read.qxmd.com/read/34751961/genes-identified-in-rodent-studies-of-alcohol-intake-are-enriched-for-heritability-of-human-substance-use
#28
JOURNAL ARTICLE
Spencer B Huggett, Emma C Johnson, Alexander S Hatoum, Dongbing Lai, Jenani Srijeyanthan, Jason A Bubier, Elissa J Chesler, Arpana Agrawal, Abraham A Palmer, Howard J Edenberg, Rohan H C Palmer
BACKGROUND: Rodent paradigms and human genome-wide association studies (GWAS) on drug use have the potential to provide biological insight into the pathophysiology of addiction. METHODS: Using GeneWeaver, we created rodent alcohol and nicotine gene-sets derived from 19 gene expression studies on alcohol and nicotine outcomes. We partitioned the SNP-heritability of these gene-sets using four large human GWAS: 1) alcoholic drinks per week, 2) problematic alcohol use, 3) cigarettes per day and 4) smoking cessation...
November 9, 2021: Alcoholism, Clinical and Experimental Research
https://read.qxmd.com/read/34591233/mapping-of-qtl-for-agronomic-traits-using-high-density-snps-with-an-ril-population-in-maize
#29
JOURNAL ARTICLE
Kyu Jin Sa, Ik-Young Choi, Jong Yeol Park, Jae-Keun Choi, Si-Hwan Ryu, Ju Kyong Lee
BACKGROUND: Genome wide association studies (GWAS) have been widely used to identify QTLs underlying quantitative traits in humans and animals, and they have also become a popular method of mapping QTLs in many crops, including maize. Advances in high-throughput genotyping technologies enable construction of high-density linkage maps using SNP markers. OBJECTIVES: High-density genetic mapping must precede to find molecular markers associated with a particular trait...
September 30, 2021: Genes & Genomics
https://read.qxmd.com/read/34411106/genome-scans-of-facial-features-in-east-africans-and-cross-population-comparisons-reveal-novel-associations
#30
JOURNAL ARTICLE
Chenxing Liu, Myoung Keun Lee, Sahin Naqvi, Hanne Hoskens, Dongjing Liu, Julie D White, Karlijne Indencleef, Harold Matthews, Ryan J Eller, Jiarui Li, Jaaved Mohammed, Tomek Swigut, Stephen Richmond, Mange Manyama, Benedikt Hallgrímsson, Richard A Spritz, Eleanor Feingold, Mary L Marazita, Joanna Wysocka, Susan Walsh, Mark D Shriver, Peter Claes, Seth M Weinberg, John R Shaffer
Facial morphology is highly variable, both within and among human populations, and a sizable portion of this variation is attributable to genetics. Previous genome scans have revealed more than 100 genetic loci associated with different aspects of normal-range facial variation. Most of these loci have been detected in Europeans, with few studies focusing on other ancestral groups. Consequently, the degree to which facial traits share a common genetic basis across diverse sets of humans remains largely unknown...
August 2021: PLoS Genetics
https://read.qxmd.com/read/34332553/genomic-signatures-of-natural-selection-at-phenology-related-genes-in-a-widely-distributed-tree-species-fagus-sylvatica-l
#31
JOURNAL ARTICLE
Joanna Meger, Bartosz Ulaszewski, Jaroslaw Burczyk
BACKGROUND: Diversity among phenology-related genes is predicted to be a contributing factor in local adaptations seen in widely distributed plant species that grow in climatically variable geographic areas, such as forest trees. European beech (Fagus sylvatica L.) is widespread, and is one of the most important broadleaved tree species in Europe; however, its potential for adaptation to climate change is a matter of uncertainty, and little is known about the molecular basis of climate change-relevant traits like bud burst...
July 31, 2021: BMC Genomics
https://read.qxmd.com/read/33978749/assessment-of-significance-of-conditionally-independent-gwas-signals
#32
JOURNAL ARTICLE
Sahar Ghasemi, Alexander Teumer, Matthias Wuttke, Tim Becker
MOTIVATION: Multiple independently associated SNPs within a linkage disequilibrium (LD) region are a common phenomenon. Conditional analysis has been successful in identifying secondary signals. While conditional association tests are limited to specific genomic regions, they are benchmarked with genome-wide scale criterion, a conservative strategy. METHOD: Within the weighted hypothesis testing framework, we developed a "quasi-adaptive" method that uses the pairwise correlation (r2) and physical distance (d) from the index association to construct priority functions G = G(r2, d), which assign a SNP-specific α-threshold to each SNP...
May 12, 2021: Bioinformatics
https://read.qxmd.com/read/33680896/can-silver-diamine-fluoride-or-silver-nanoparticle-based-anticaries-agents-to-affect-enamel-bond-strength
#33
JOURNAL ARTICLE
Jaqueline Costa Favaro, Yana Cosendey Toledo de Mello Peixoto, Omar Geha, Flaviana Alves Dias, Ricardo Danil Guiraldo, Murilo Baena Lopes, Sandrine Bittencourt Berger
OBJECTIVES: The aim of the current study is to investigate the effect of different anticaries agents, such as experimental agents based on silver nanoparticles (SNPs) and silver diamine fluoride (SDF), on the micro-shear bond strength (μ-SBS) of composite resin applied to intact enamel (IE) or demineralized enamel (DE). MATERIALS AND METHODS: Sixty dental enamel fragments were collected from human third molars and categorized into 6 groups ( n = 10): positive control (IE), negative control (DE), IE + SDF, DE + SDF, IE + SNP and DE + SNP...
February 2021: Restorative Dentistry & Endodontics
https://read.qxmd.com/read/33664403/quantifying-genetic-heterogeneity-between-continental-populations-for-human-height-and-body-mass-index
#34
JOURNAL ARTICLE
Jing Guo, Andrew Bakshi, Ying Wang, Longda Jiang, Loic Yengo, Michael E Goddard, Peter M Visscher, Jian Yang
Genome-wide association studies (GWAS) in samples of European ancestry have identified thousands of genetic variants associated with complex traits in humans. However, it remains largely unclear whether these associations can be used in non-European populations. Here, we seek to quantify the proportion of genetic variation for a complex trait shared between continental populations. We estimated the between-population correlation of genetic effects at all SNPs ([Formula: see text]) or genome-wide significant SNPs ([Formula: see text]) for height and body mass index (BMI) in samples of European (EUR; [Formula: see text]) and African (AFR; [Formula: see text]) ancestry...
March 4, 2021: Scientific Reports
https://read.qxmd.com/read/33611520/imputed-gene-expression-risk-scores-a-functionally-informed-component-of-polygenic-risk
#35
JOURNAL ARTICLE
Oliver Pain, Kylie P Glanville, Saskia Hagenaars, Saskia Selzam, Anna Fürtjes, Jonathan R I Coleman, Kaili Rimfeld, Gerome Breen, Lasse Folkersen, Cathryn M Lewis
BACKGROUND: Integration of functional genomic annotations when estimating polygenic risk scores (PRS) can provide insight into aetiology and improve risk prediction. This study explores the predictive utility of gene expression risk scores (GeRS), calculated using imputed gene expression and transcriptome-wide association study (TWAS) results. METHODS: The predictive utility of GeRS was evaluated using 12 neuropsychiatric and anthropometric outcomes measured in two target samples: UK Biobank and the Twins Early Development Study (TEDS)...
February 22, 2021: Human Molecular Genetics
https://read.qxmd.com/read/33501449/protein-coding-repeat-polymorphisms-strongly-shape-diverse-human-phenotypes
#36
Ronen E Mukamel, Robert E Handsaker, Maxwell A Sherman, Alison R Barton, Yiming Zheng, Steven A McCarroll, Po-Ru Loh
Hundreds of the proteins encoded in human genomes contain domains that vary in size or copy number due to variable numbers of tandem repeats (VNTRs) in protein-coding exons. VNTRs have eluded analysis by the molecular methods-SNP arrays and high-throughput sequencing-used in large-scale human genetic studies to date; thus, the relationships of VNTRs to most human phenotypes are unknown. We developed ways to estimate VNTR lengths from whole-exome sequencing data, identify the SNP haplotypes on which VNTR alleles reside, and use imputation to project these haplotypes into abundant SNP data...
January 19, 2021: bioRxiv
https://read.qxmd.com/read/33324447/haplotype-analysis-of-genomic-prediction-using-structural-and-functional-genomic-information-for-seven-human-phenotypes
#37
JOURNAL ARTICLE
Zuoxiang Liang, Cheng Tan, Dzianis Prakapenka, Li Ma, Yang Da
Genomic prediction using multi-allelic haplotype models improved the prediction accuracy for all seven human phenotypes, the normality transformed high density lipoproteins, low density lipoproteins, total cholesterol, triglycerides, weight, and the original height and body mass index without normality transformation. Eight SNP sets with 40,941-380,705 SNPs were evaluated. The increase in prediction accuracy due to haplotypes was 1.86-8.12%. Haplotypes using fixed chromosome distances had the best prediction accuracy for four phenotypes, fixed number of SNPs for two phenotypes, and gene-based haplotypes for high density lipoproteins and height (tied for best)...
2020: Frontiers in Genetics
https://read.qxmd.com/read/33089531/all-sheeps-and-sizes-a-genetic-investigation-of-mature-body-size-across-sheep-breeds-reveals-a-polygenic-nature
#38
JOURNAL ARTICLE
C J Posbergh, H J Huson
Mature body size is genetically correlated with growth rate, an important economic trait in the sheep industry. Mature body size has been studied extensively in humans as well as cattle and other domestic animal populations but not in sheep. Six-hundred and sixteen ewes, across 22 breeds, were measured for 28 linear measurements representing various skeletal parts. PCA from these measures generated principal components 1 and 2 which represented 66 and 7% of the phenotypic variation respectively. Two-hundred and twenty sheep were genotyped on the Illumina Ovine HD beadchip for a GWAS investigating mature body size and linear body measurements...
October 21, 2020: Animal Genetics
https://read.qxmd.com/read/32764582/sibling-validation-of-polygenic-risk-scores-and-complex-trait-prediction
#39
JOURNAL ARTICLE
Louis Lello, Timothy G Raben, Stephen D H Hsu
We test 26 polygenic predictors using tens of thousands of genetic siblings from the UK Biobank (UKB), for whom we have SNP genotypes, health status, and phenotype information in late adulthood. Siblings have typically experienced similar environments during childhood, and exhibit negligible population stratification relative to each other. Therefore, the ability to predict differences in disease risk or complex trait values between siblings is a strong test of genomic prediction in humans. We compare validation results obtained using non-sibling subjects to those obtained among siblings and find that typically most of the predictive power persists in between-sibling designs...
August 6, 2020: Scientific Reports
https://read.qxmd.com/read/32640102/base-editing-with-high-efficiency-in-allotetraploid-oilseed-rape-by-a3a-pbe-base-editing-system
#40
JOURNAL ARTICLE
Hongtao Cheng, Mengyu Hao, Bingli Ding, Desheng Mei, Wenxiang Wang, Hui Wang, Rijin Zhou, Jia Liu, Chao Li, Qiong Hu
CRISPR/Cas- base editing is an emerging technology that could convert a nucleotide to another type at the target site. In this study, A3A-PBE system consisting of human A3A cytidine deaminase fused with a Cas9 nickase and uracil glycosylase inhibitor, was established and developed in allotetraploid Brassica napus. We designed three sgRNAs to target ALS, RGA and IAA7 genes, respectively. Base editing efficiency was demonstrated to be more than 20% for all of the three target genes. Target sequencing results revealed that the editing window ranged from C1 to C10 of the PAM sequence...
July 8, 2020: Plant Biotechnology Journal
keyword
keyword
4675
2
3
Fetch more papers »
Fetching more papers... Fetching...
Remove bar
Read by QxMD icon Read
×

Save your favorite articles in one place with a free QxMD account.

×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"

We want to hear from doctors like you!

Take a second to answer a survey question.