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Journal articles on the topic 'Molecular genetic data'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Atramentova, L., and H. Ehyakonandeh. "Molecular genetic data in terms of associative and population genetics." 36, no. 36 (August 25, 2021): 35–40. http://dx.doi.org/10.26565/2075-5457-2021-36-4.

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In studies on associative genetics of various multifactorial diseases, it is most often found that the minor allele’s frequency in the group of patients is higher than in the group of healthy people. Due to reduced adaptation, the minor allele manifests itself as a disease. In the group of patients, the number of homozygotes by major allele is reduced, the number of heterozygous carriers of the provocative allele is increased, and the frequency of homozygotes by the provocative allele is significantly increased. The aim of this article was to analyze the unusual result for SNP 1298A/C of the M

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2

WEIR, B. S. "Statistical Analysis of Molecular Genetic Data." Mathematical Medicine and Biology 2, no. 1 (1985): 1–39. http://dx.doi.org/10.1093/imammb/2.1.1.

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Berrebi, Patrick, and Petr Ráb. "III‐Cytogenetic and molecular genetic data." Italian Journal of Zoology 65, sup1 (1998): 15–20. http://dx.doi.org/10.1080/11250009809386790.

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4

Butler, Amy W., Sarah Cohen-Woods, Anne Farmer, Peter McGuffin, and Cathryn M. Lewis. "Integrating Phenotypic Data For Depression." Journal of Integrative Bioinformatics 7, no. 3 (2010): 290–99. http://dx.doi.org/10.1515/jib-2010-136.

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Abstract The golden era of molecular genetic research brings about an explosion of phenotypic, genotypic and sequencing data. Building on the common aims to exploit understanding of human diseases, it also opens up an opportunity for scientific communities to share and combine research data. Genome-wide association studies (GWAS) have been widely used to locate genetic variants, which are susceptible for common diseases. In the field of medical genetics, many international collaborative consortiums have been established to conduct meta-analyses of GWAS results and to combine large genotypic da

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Beauchamp, Jonathan P., David Cesarini, Magnus Johannesson, et al. "Molecular Genetics and Economics." Journal of Economic Perspectives 25, no. 4 (2011): 57–82. http://dx.doi.org/10.1257/jep.25.4.57.

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The costs of comprehensively genotyping human subjects have fallen to the point where major funding bodies, even in the social sciences, are beginning to incorporate genetic and biological markers into major social surveys. How, if at all, should economists use and combine molecular genetic and economic data from these surveys? What challenges arise when analyzing genetically informative data? To illustrate, we present results from a “genome-wide association study” of educational attainment. We use a sample of 7,500 individuals from the Framingham Heart Study; our dataset contains over 360,000

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HELLARD, S., C. A. M. SEMPLE, S. W. MORRIS, D. J. PORTEOUS, and K. L. EVANS. "Physical mapping: integrating computational and molecular genetic data." Annals of Human Genetics 65, no. 3 (2001): 221–28. http://dx.doi.org/10.1046/j.1469-1809.2001.6530221.x.

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LE HELLARD, S., C. A. M. SEMPLE, S. W. MORRIS, D. J. PORTEOUS, and K. L. EVANS. "Physical mapping: integrating computational and molecular genetic data." Annals of Human Genetics 65, no. 3 (2001): 221–28. http://dx.doi.org/10.1017/s0003480001008594.

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Domingo-Roura, X., J. Marmi, J. F. López-Giráldez, and E. García-Franquesa. "New molecular challenges in animal conservation." Animal Biodiversity and Conservation 24, no. 1 (2001): 19–29. https://doi.org/10.32800/abc.2001.24.0019.

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The contribution of genetics to wildlife conservation has been stressed often forgetting the existing theoretical and empirical limitations in the use of genetic information to solve ecological and demographic problems. The possibilities of molecular analyses are extensive and the automation of procedures is increasing the efficiency and reducing the cost of molecular technology. With large amounts of molecular data already available, the interest is switching towards the analysis of these data and the interpretation of genetic variability within and across species from a functional perspectiv

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Shields, Denis C., and Aisling M. O'Halloran. "Integrating Genotypic Data with Transcriptomic and Proteomic Data." Comparative and Functional Genomics 3, no. 1 (2002): 22–27. http://dx.doi.org/10.1002/cfg.135.

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Historically genotypic variation has been detected at the phenotypic level, at the metabolic level, and at the protein chemistry level. Advances in technology have allowed its direct visualisation at the level of DNA variation. Nevertheless, there is still an enormous interest in phenotypic, metabolic and protein property variability, since such variation gives insights into potential functionally important differences conferred by genetic variation. High-throughput transcriptomics and proteomics applied to different individuals drawn from a population has the potential to identify the functio

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Chesnokov, Yu V. "GENETIC MARKERS: COMPARATIVE CLASSIFICATION OF MOLECULAR MARKERS." Vegetable crops of Russia, no. 3 (July 25, 2018): 11–15. http://dx.doi.org/10.18619/2072-9146-2018-3-11-15.

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With the creation of the molecular markers allowing to carry out analysis of genotypes on the level initial genetic information – DNA, onset one of the most multifarious and one of the most large in number class of markers at the present day. It is concerned with that each separate nucleic acid sequence is unique on its structure. Set of molecular and genetic methods, named as DNA-fingerprinting, most wide used in modern investigations for solving different problems in different biological areas. In this connection, necessity in comparative classification of modern molecular and genetic marker

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Labate, Joanne A. "Software for Population Genetic Analyses of Molecular Marker Data." Crop Science 40, no. 6 (2000): 1521–28. http://dx.doi.org/10.2135/cropsci2000.4061521x.

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Duran, Chris, Nikki Appleby, David Edwards, and Jacqueline Batley. "Molecular Genetic Markers: Discovery, Applications, Data Storage and Visualisation." Current Bioinformatics 4, no. 1 (2009): 16–27. http://dx.doi.org/10.2174/157489309787158198.

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13

Laurentin, Hernán. "Data analysis for molecular characterization of plant genetic resources." Genetic Resources and Crop Evolution 56, no. 2 (2009): 277–92. http://dx.doi.org/10.1007/s10722-008-9397-8.

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14

Marjoram, Paul, and Simon Tavaré. "Modern computational approaches for analysing molecular genetic variation data." Nature Reviews Genetics 7, no. 10 (2006): 759–70. http://dx.doi.org/10.1038/nrg1961.

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15

Imsiridou, A. "Web Database of Molecular Genetic Data From Fish Stocks." Journal of Heredity 94, no. 3 (2003): 265–67. http://dx.doi.org/10.1093/jhered/esg057.

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Henrikson, Nora B., Stephanie M. Fullerton, Aaron Scrol, Lorella Palazzo, Marlaine Figueroa Gray, and Paula R. Blasi. "“Not Private at All:” Comparative Perspectives on Privacy of Genomic Data, Family History Data, Health-Related Data, and Other Personal Data." OBM Genetics 06, no. 04 (2022): 1–17. http://dx.doi.org/10.21926/obm.genet.2204167.

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People choose how and if to generate and disclose not just personal genomic data, but also multiple other types of personal health and non-health related data. To contextualize choices about genetic testing and genetic data disclosure, we explored perspectives of genomic data privacy and disclosure compared to other types of data. We conducted a qualitative focus group study with adult members of an integrated U.S. health system, using administrative data to stratify our sample by age and by race/ethnicity. Discussion topics included qualities, rights, benefits and harms of disclosure of genom

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Feytmans, E., and B. S. Weir. "Genetic Data Analysis: Methods for Discrete Population Genetic Data." Biometrics 47, no. 3 (1991): 1205. http://dx.doi.org/10.2307/2532683.

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SHEIDAI, MASOUD, HANIYEH TEYMOORI, ZAHRA NOORMOHAMMADI, AHMAD-REZA MEHRABIAN, FAHIMEH KOOHDAR, and SOMAYEH GHASEMZADEH-BARAKI. "Species delimitation in the genus Tamarix: Morphological and molecular data." Phytotaxa 343, no. 2 (2018): 101. http://dx.doi.org/10.11646/phytotaxa.343.2.1.

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Tamarix (Tamaricaceae) is an ancient genus in Asia that contains about 54 to 90 species with unresolved taxonomy. Tamarix has major center of speciation in the Pakistan-Afghanistan-Iran-Turkmenistan-S-Kazakhstan-W-China area and in the eastern Mediterranean area. Tamarix species are highly plastic and tolerant to adversity being able to occupy different habitats, thus showing a wide range of ecological variations. Tamarix species have commercial value in the landscape and horticultural trade and are planted for erosion control and as wind breaks. In the genus Tamarix, many species are morpholo

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19

Lewontin, R. C. "The detection of linkage disequilibrium in molecular sequence data." Genetics 140, no. 1 (1995): 377–88. http://dx.doi.org/10.1093/genetics/140.1.377.

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Abstract Studies of genetic variation in natural populations at the sequence level usually show that most polymorphic sites are very asymmetrical in allele frequencies, with the rarer allele at a site near fixation. When the rarer allele at a site is present only a few times in the sample, say below five representatives, it becomes very difficult to detect linkage disequilibrium between sites from tests of association. This is a consequence of the numerical properties of even the most powerful test of association, Fisher's exact test. Sites with fewer than five representatives in the sample sh

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A.A., Hamrayev, and Yuldasheva D.H. "Laboratory And Molecular-Genetic Markers Of The Progression Of Non-Alcoholic Fatty Liver Disease (literature review and own data)." American Journal of Medical Sciences and Pharmaceutical Research 03, no. 03 (2021): 75–82. http://dx.doi.org/10.37547/tajmspr/volume03issue03-11.

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Non-alcoholic fatty liver disease (NAFLD) is one of the most common diseases in hepatology. First of all, this is associated with a high risk of progression of NAFLD with the development of non-alcoholic steatohepatitis (NASH), liver failure, and hepatocellular carcinoma. Epidemiological and genetic studies have shown the relationship between the morphological stage of NAFLD and hereditary factors. The article provides a review of the literature on the cytokines, MBOAT7 and GCKR genes. Also, a variant of the MBOAT7 and GCKR gene is associated with a high risk of fibrosis in patients with NAFLD

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D, Bhuvana. "Innovations in Molecular Biology-Cutting-Edge Breakthroughs in Molecular Genetics." Annals of Experimental and Molecular Biology 6, no. 1 (2024): 1–4. http://dx.doi.org/10.23880/aemb-16000121.

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The field of molecular biology has experienced significant breakthroughs in recent years, driven by cutting-edge technologies and innovative research strategies. This abstract provides a concise overview of some key advancement that has shaped the landscape of molecular biology. One prominent area of progress involves the CRISPR-Cas9 gene editing system, which has revolutionized genetic manipulation. Researchers have refined and expanded its applications, enabling precise modifications to the genome for therapeutic purposes, functional genomics, and the development of genetically modified orga

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Abramson, Nataliya. "The Origin of the Przewalski’s Horse: a Molecular Genetic Data." Priroda, no. 7 (2018): 5–8. http://dx.doi.org/10.31857/s0032874x0000251-5.

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Verma, Anamika, and Dhirendra Singh. "Analysing Solanum tuberosum L. Genetic Divergence using Molecular Marker Data." International Journal of Environment, Agriculture and Biotechnology 5, no. 3 (2020): 760–72. http://dx.doi.org/10.22161/ijeab.53.29.

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Chernetskaya, D. M., E. A. Likhacheva, O. S. Pshenichnikova, V. L. Surin, and N. I. Zozulya. "VON WILLEBRAND DISEASE: CLINICAL, COAGULOGICAL, MOLECULAR AND GENETIC DATA COMPARISON." Russian journal of hematology and transfusiology 64, no. 3 (2019): 246–55. http://dx.doi.org/10.35754/0234-5730-2019-64-3-246-255.

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Introduction. Von Willebrand disease (vWD) — one of the most common coagulopathies — is characterised by a rather complicated inheritance pattern, which can be either dominant or recessive depending on the disease type. Aim. To compare clinical, coagulological and molecular genetic data obtained when examining patients with various types of vWD.Materials and methods. The vWF gene exons were sequenced in 16 patients suffering from VWD using the Sanger method.Results. In total, 12 various mutations were identified, one of which (Pro2527His) has not been previously observed in the world populatio

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Selinski, Silvia, and Katja Ickstadt. "Cluster Analysis of Genetic and Epidemiological Data in Molecular Epidemiology." Journal of Toxicology and Environmental Health, Part A 71, no. 11-12 (2008): 835–44. http://dx.doi.org/10.1080/15287390801985828.

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26

Ladanyi, Marc, and Julia A. Bridge. "Contribution of molecular genetic data to the classification of sarcomas." Human Pathology 31, no. 5 (2000): 532–38. http://dx.doi.org/10.1053/hp.2000.6706.

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Horsburgh, K. Ann. "Molecular anthropology: the judicial use of genetic data in archaeology." Journal of Archaeological Science 56 (April 2015): 141–45. http://dx.doi.org/10.1016/j.jas.2015.02.033.

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Faraji-Rad, Mohammad. "Epidemiological Study of Molecular and Genetic Classification in Adult Diffuse Glioma." International Journal of Surgery & Surgical Techniques 6, no. 2 (2022): 1–5. http://dx.doi.org/10.23880/ijsst-16000171.

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Background: Mutations in isocitrate dehydrogenase 1 (IDH1) and isocitrate dehydrogenase 2 (IDH2) are frequent in lowgrade and high-grade gliomas. However, the diagnostic criteria, in particular for gliomas, are highly various. The aim of our study was to establish genetic profiles for mutation and calcification of diffuse gliomas and to evaluate their predictive factors. Methods: We estimate the different clinical and molecular characterization between IDH1, IDH2 mutant gliomas, p53, ATRX and 1p19q. In addition, whole-transcriptome sequencing and DNA extraction data were used to evaluate the d

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Schadt, E. E., S. A. Monks, and S. H. Friend. "A new paradigm for drug discovery: integrating clinical, genetic, genomic and molecular phenotype data to identify drug targets." Biochemical Society Transactions 31, no. 2 (2003): 437–43. http://dx.doi.org/10.1042/bst0310437.

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Application of statistical genetics approaches to variations in mRNA transcript abundances in segregating populations can be used to identify genes and pathways associated with common human diseases. The combination of this genetic information with gene expression and clinical trait data can also be used to identify subtypes of a disease and the genetic loci specific to each subtype. Here we highlight results from some of our recent work in this area and further explore the many possibilities that exist in employing a more comprehensive genetics and functional genomics approach to the function

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Slobodan, Tofiloski. "Navigating the Ethical Landscape of Molecular Psychiatry and Behavioral Genetics." Contemporary Research Analysis Journal 02, no. 04 (2025): 210–19. https://doi.org/10.5281/zenodo.15267761.

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ABSTRACT: This paper explores the intricate ethical considerations within the fields of behavioral genetics and molecular psychiatry, emphasizing the necessity for careful deliberation and active engagement in navigating the complex ethical landscape of genetic and molecular research on behavior and mental health. Through a comprehensive literature review, the analysis highlights the dual nature of this type of researches: their potential to provide groundbreaking insights into mental disorders and their ethical challenges, including issues of privacy, consent, and the responsible use of sensi

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Corrado, Giandomenico, Maurizio La Mura, Orsola Ambrosino, Giuseppe Pugliano, Paola Varricchio, and Rosa Rao. "Relationships of Campanian olive cultivars: comparative analysis of molecular and phenotypic data." Genome 52, no. 8 (2009): 692–700. http://dx.doi.org/10.1139/g09-044.

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Estimation of the genetic relatedness of traditional olive cultivars with genetic markers and phenotypic data enables progress in plant breeding, management of genetic resources, and protection of both breeders’ rights and certified premium products. We used amplified fragment length polymorphisms (AFLPs), simple sequence repeats (SSRs), and quantitative and qualitative morphological traits, including characteristics recommended for variety registration, to study genetic diversity and relationships in the olive at different levels. The 14 varieties analyzed, which are used for the production o

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Cruz-Utrilla, Alejandro, Natalia Gallego-Zazo, Jair Antonio Tenorio-Castaño, et al. "Clinical Implications of the Genetic Background in Pediatric Pulmonary Arterial Hypertension: Data from the Spanish REHIPED Registry." International Journal of Molecular Sciences 23, no. 18 (2022): 10433. http://dx.doi.org/10.3390/ijms231810433.

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Background: Pulmonary arterial hypertension (PAH) is a severe and rare disease with an important genetic background. The influence of genetic testing in the clinical classification of pediatric PAH is not well known and genetics could influence management and prognosis. Objectives: The aim of this work was to identify the molecular fingerprint of PH children in the REgistro de pacientes con HIpertensión Pulmonar PEDiátrica (REHIPED), and to investigate if genetics could have an impact in clinical reclassification and prognosis. Methods: We included pediatric patients with a genetic analysis fr

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Kotov, S. V., A. L. Khachatryan, and Sh M. Sargsyan. "Molecular genetic subtypes of bladder cancer." Urology Herald 11, no. 3 (2023): 108–17. http://dx.doi.org/10.21886/2308-6424-2023-11-3-108-117.

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Introduction. Bladder cancer (BCa) is one of the most common oncological diseases with many relapses and progressions, which requires more and more new ways to solve this problem.Objective. To analyse of existing data on the molecular and genetic features of BCa classification based on them, assessment of the possibility of its introduction into clinical practice as a criterion for recurrence and progression.Materials & methods. We analysed the data of studies on molecular subtypes of BCa published in PubMed, Scientific Electronic Library of Russia (eLibrary), Scopus, Medline, EMBASE, webs

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Kubyshkin, A. V., G. M. Salieva, I. I. Fomochkina, and D. I. Vodolazhsky. "Molecular genetic testing in ovarian cancer." Pacific Medical Journal, no. 4 (January 17, 2023): 11–18. http://dx.doi.org/10.34215/1609-1175-2022-4-11-18.

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Ovarian cancer (OC) remains to be a leading cause of mortality among oncogynaecological patients. The low five-year survival rate of OC patients is associated with a lack of highly sensitive screening, early diagnostics and preventive methods, as well as high metastasis, recurrence and chemoresistance rates. Molecular genetic techniques for OC diagnosis based on standardized genetic panels can be used to detect a limited range of mutations in the BRCA1 and BRCA2 genes. However, the spectrum of genes potentially responsible for OC development is much wider. Recent data emphasize the importance

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Alsiddig Ahmed, Asaad. "Molecular Genetic Identification of Some Sweet Sorghum - Sorghum bicolor L. (Ankolib) Accessions - Sudan." International Journal of Stem Cells and Medicine 2, no. 1 (2023): 01–04. http://dx.doi.org/10.58489/2836-5038/007.

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This study is an attempt to identify some Sudanese Sweet Sorghum (Ankolib) [Sorghum bicolor (L.) Moench.] accessions using two types of DNA-based markers: RAPD and SSR. Seven (Ankolib) accessions were assayed, namely: Black Ankolib, Black White Ankolib, Dark Red Ankolib, Red Yellow Ankolib, White Ankolib, White Black Ankolib and Bengaga. All of the accessions were uniquely identified and fingerprinted. The levels of polymorphism among the accessions as revealed by (22) RAPD primers and (16) SSR primer pairs were (58%) and (76%) respectively, indicating that SSRs markers were highly polymorphic

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Lawrence, J. G., and D. L. Hartl. "Inference of horizontal genetic transfer from molecular data: an approach using the bootstrap." Genetics 131, no. 3 (1992): 753–60. http://dx.doi.org/10.1093/genetics/131.3.753.

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Abstract Inconsistencies in taxonomic relationships implicit in different sets of nucleic acid sequences potentially result from horizontal transfer of genetic material between genomes. A nonparametric method is proposed to determine whether such inconsistencies are statistically significant. A similarity coefficient is calculated from ranked pairwise identities and evaluated against a distribution of similarity coefficients generated from resampled data. Subsequent analyses of partial data sets, obtained by the elimination of individual taxa, identify particular taxa to which the significance

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Scicchitano, Pietro, Francesca Amati, Marco Matteo Ciccone, et al. "Hypertriglyceridemia: Molecular and Genetic Landscapes." International Journal of Molecular Sciences 25, no. 12 (2024): 6364. http://dx.doi.org/10.3390/ijms25126364.

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Lipid disorders represent one of the most worrisome cardiovascular risk factors. The focus on the impact of lipids on cardiac and vascular health usually concerns low-density lipoprotein cholesterol, while the role of triglycerides (TGs) is given poor attention. The literature provides data on the impact of higher plasma concentrations in TGs on the cardiovascular system and, therefore, on the outcomes and comorbidities of patients. The risk for coronary heart diseases varies from 57 to 76% in patients with hypertriglyceridemia. Specifically, the higher the plasma concentrations in TGs, the hi

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38

Mkrtchyan, L. A., Y. S. Slesarenko, I. A. Yakovlev, S. N. Bardakov, and R. V. Deev. "Molecular and genetic features of calpainopathy." Genes & Cells 17, no. 2 (2022): 6–13. http://dx.doi.org/10.23868/202209001.

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Calpainopathy is the most common form of limb-girdle muscular dystrophy, prevalence in the population is approximately 1 in 15,00042,700 individuals. In the Russian Federation, there is an insufficient number of studies, which researched prevalence of calpainopathy among patients with limb-girdle muscular dystrophy, but according to available data, approximately in 43% of cases the disease is associated with mutations of the CAPN3 gene. Molecular genetic analysis is the main method for diagnosing these patients. Studies indicate many pathogenic mutations that cause calpainopathy with correspon

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Butnariu, Lăcramioara Ionela, Eusebiu Vlad Gorduza, Elena Țarcă, et al. "Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome." Diagnostics 13, no. 14 (2023): 2348. http://dx.doi.org/10.3390/diagnostics13142348.

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Atherogenic dyslipidemia plays a critical role in the development of metabolic syndrome (MetS), being one of its major components, along with central obesity, insulin resistance, and hypertension. In recent years, the development of molecular genetics techniques and extended analysis at the genome or exome level has led to important progress in the identification of genetic factors (heritability) involved in lipid metabolism disorders associated with MetS. In this review, we have proposed to present the current knowledge related to the genetic etiology of atherogenic dyslipidemia, but also pos

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Zampatti, Stefania, Michele Ragazzo, Cristina Peconi, et al. "Genetic Counselling Improves the Molecular Characterisation of Dementing Disorders." Journal of Personalized Medicine 11, no. 6 (2021): 474. http://dx.doi.org/10.3390/jpm11060474.

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Dementing disorders are a complex group of neurodegenerative diseases characterised by different, but often overlapping, pathological pathways. Genetics have been largely associated with the development or the risk to develop dementing diseases. Recent advances in molecular technologies permit analyzing of several genes in a small time, but the interpretation analysis is complicated by several factors: the clinical complexity of neurodegenerative disorders, the frequency of co-morbidities, and the high phenotypic heterogeneity of genetic diseases. Genetic counselling supports the diagnostic pa

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Wang, Yishu, Lin Wang, Dejie Yang, and Minghua Deng. "Imputing missing values for genetic interaction data." Methods 67, no. 3 (2014): 269–77. http://dx.doi.org/10.1016/j.ymeth.2014.03.032.

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Martschenko, Daphne, Sam Trejo, and Benjamin W. Domingue. "Genetics and Education: Recent Developments in the Context of an Ugly History and an Uncertain Future." AERA Open 5, no. 1 (2019): 233285841881051. http://dx.doi.org/10.1177/2332858418810516.

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Driven by our recent mapping of the human genome, genetics research is increasingly prominent and beginning to reintersect with education research. We describe previous intersections of these fields, focusing on the ways that they were harmful. We then discuss novel features of genetics research in the current era, with an emphasis on possibilities deriving from the availability of molecular genetic data and the proliferation of genome-wide association studies. We discuss both the promises and potential pitfalls resulting from the convergence of molecular genetic research and education researc

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Tiväng, Jan, Jim Nienhuis, and O. S. Smith. "SAMPLING VARIANCE FOR MOLECULAR MARKER DATA WITH RESPECT TO GENETIC DISTANCE." HortScience 27, no. 6 (1992): 573f—573. http://dx.doi.org/10.21273/hortsci.27.6.573f.

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The sampling method was applied to a data-set generated by RFLP molecular marker analysis, representing 37 Zea maize cultivars. A total of 251 enzyme probe-combinations were used yielding a total of 1,205 scores per genotype. Genetic distance was calculated among all 37 entries from subsets of arbitrary and increasing sample size. Each score entry in the subset was selected at random from all possible scores with replacement following each selection. The variance for genetic distance was calculated among all subsets of equal size for all possible cultivar pairs. The pooled pair variance was pl

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Belyaeva, T. M., I. V. Ponomarenko, and M. I. Churnosov. "Molecular-genetic determinants of atopic dermatitis (data from genome-wide studies)." Klinicheskaya dermatologiya i venerologiya 19, no. 5 (2020): 615. http://dx.doi.org/10.17116/klinderma202019051615.

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ahmed, alaa, Ibrahim ELSemman, Ameer ELFarash, and Sara Mohamed. "Auto Calculation of Genetic Diversity Measures Based on Molecular Markers Data." Recent Research in Genetics and Genomics 4, no. 2 (2022): 1–16. http://dx.doi.org/10.21608/rrgg.2022.156544.1010.

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Conley, Dalton, and Benjamin Domingue. "The Bell Curve Revisited: Testing Controversial Hypotheses with Molecular Genetic Data." Sociological Science 3 (2016): 520–39. http://dx.doi.org/10.15195/v3.a23.

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SAMPAYO, E. M., S. DOVE, and T. C. LAJEUNESSE. "Cohesive molecular genetic data delineate species diversity in the dinoflagellate genusSymbiodinium." Molecular Ecology 18, no. 3 (2009): 500–519. http://dx.doi.org/10.1111/j.1365-294x.2008.04037.x.

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BOYACI, Hatice Filiz, Volkan TOPCU, Akin TEPE, Isilay Karasahin YILDIRIM, Mehmet OTEN, and Aytekin AKTAS. "Morphological and Molecular Characterization and Relationships of Turkish Local Eggplant Heirlooms." Notulae Botanicae Horti Agrobotanici Cluj-Napoca 43, no. 1 (2015): 100–107. http://dx.doi.org/10.15835/nbha4319773.

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A total of 38 eggplant genotypes, of which 32 were heirloom accessions collected from different regions of Burdur province five were different local genotypes from other provinces, and one was a cultivar, were used as reference in this study. The phylogenetic relationships among these heirlooms were evaluated using 40 morphologic descriptors and five randomly amplified polymorphic RAPD markers. The horizontal dendrograms were created by using UPGMA with both morphologic and molecular data. Burdur heirloom accessions showed high genetic diversity based on morphological and molecular data. The g

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Schön, Isa, and Koen Martens. "Phylogenetic Reconstructions of Ostracodes – A Molecular Approach." Paleontological Society Papers 9 (November 2003): 71–88. http://dx.doi.org/10.1017/s1089332600002151.

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Molecular work on ostracodes has thus far either used allozyme-based or DNA-based techniques. The application of allozyme-based methods has provided numerous data on population genetics and reproductive modes in ostracodes. With this technique, it has also been possible to construct phylogenies, although these have been restricted to distance-based methods. With the usage of DNA-based methods, a new era in ostracode research has begun. It is now possible to obtain accurate estimates for genetic diversities at very fine scales, even within individuals. The DNA-based approach is also very useful

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Nikitin, P. V., M. V. Ryzhova, A. A. Potapov, et al. "Glioblastoma molecular and histological heterogeneity." CLINICAL AND EXPERIMENTAL MORPHOLOGY 9, no. 3 (2020): 5–11. http://dx.doi.org/10.31088/cem2020.9.3.5-11.

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The heterogeneity of tumors properties is a serious diagnostic and therapeutic problem. It is manifested by the variability of genetic, proteomic and epigenetic parameters both between different samples of the same histological variant of the tumor, and between different sites within the same neoplasm with the presence of heterogeneous cell populations in this particular patient. Glioblastoma (GB) is one of the most frequent fatal tumors of the central nervous system in humans. The understanding the intertumor heterogeneity is the key to the development of both new diagnostic approaches and in

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