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A Genetic Linkage Map of Mouse Chromosome 10
A Genetic Linkage Map of Mouse Chromosome 10

... AVNERet al. (1988)l. In a laboratory setting, the wild mouse species Mus spretus will interbreed with inbred laboratory mouse strains to produce fertileF1 females and sterile F1 males (BONHOMME et a l . 1984). The F1 females can then be backcrossed to generate the NB progeny used in mapping studies. ...
HL7 V2.5.1 Genetic Test Result Message
HL7 V2.5.1 Genetic Test Result Message

... genomic and healthcare IT data standards may use this guide to extend these standards for support of clinical sequencing. Users of this guide must be familiar with the details of HL7 message construction and processing. This guide is not intended to be a tutorial on that subject. ...
Potato Genome Sequencing Consortium: Final
Potato Genome Sequencing Consortium: Final

... analyse important potato traits, such as disease resistance and tuber dormancy. In some cases it will be possible to use small sets of these and related markers to select within potato breeding programmes. Now that the sequences of the ~39,000 genes in potato are known, this information can be used ...
SERIES ‘‘THE GENETIC AND CARDIOVASCULAR ASPECTS OF OBSTRUCTIVE SLEEP APNOEA/HYPOPNOEA SYNDROME’’
SERIES ‘‘THE GENETIC AND CARDIOVASCULAR ASPECTS OF OBSTRUCTIVE SLEEP APNOEA/HYPOPNOEA SYNDROME’’

... small studies that have demonstrated a worsening of SDB over variable periods of time [27, 28]. There have also been a small number of studies of the cardiovascular consequences of untreated OSAHS, which have shown increased mortality from cardiovascular and cerebrovascular disease in those with mor ...
Learning the Dominance in Diploid Genetic
Learning the Dominance in Diploid Genetic

... that are combined using a pseudo-arithmetic to determine the phenotype allele. Ryan used four genotypic alleles A, B, C, and D, and allocated the values of 2, 3, 7, and 9 to them respectively. An addition is performed on the values allocated with the two genotypic alleles for each gene locus. If the ...
Whole Exome Re-Sequencing Implicates CCDC38 and
Whole Exome Re-Sequencing Implicates CCDC38 and

... Author Summary Very large genome-wide association studies in general population cohorts have successfully identified at least 26 genes or gene regions associated with lung function and a number of these also show association with chronic obstructive pulmonary disease (COPD). However, these findings ...
2n gametes in the potato: essential ingredients for breeding and
2n gametes in the potato: essential ingredients for breeding and

... have been identified in several plant species of different taxa. The potato is probably the crop plant where they have been most intensively studied and also more appropriately used for the genetic improvement of cultivated genotypes. This paper reviews how 2n gametes allow potato breeders to broade ...
ABSTRACT Using a bioinformatics approach to identify genes that
ABSTRACT Using a bioinformatics approach to identify genes that

... protein expression in the retina and to research any diseases the gene is associated with, through MalaCards. Pathway Commons is used to gain more insight into the pathways in which the genes are involved. The result is two annotated lists of ranked genes, one related to non-RP eye phenotypes and o ...
PPT
PPT

... but rare in population; may not be reflective of common disease. Also, hard to collect family data. ...
PHI-Canto video tutorial text - PHI-base
PHI-Canto video tutorial text - PHI-base

The Maize Genome Poster
The Maize Genome Poster

... Corn, also known as maize (from the Spanish maíz), was first domesticated nearly 10,000 years ago from teosinte, a wild grass that looked quite different from our modern crop. Teosinte grew in Mexico and Central America as a bushy plant with many spikes, the precursor to our familiar ear of corn. Th ...
Identification of novel endogenous antisense transcripts by DNA
Identification of novel endogenous antisense transcripts by DNA

... by microarray analysis using AFAS probes are transcribed in vivo. We also analyzed the expression of Aard (alanine- and arginine-rich domain-containing protein), which is a functionally uncharacterized gene but is known to be expressed within the adult testis and XY fetal gonad [35]. In humans, exon ...
the x chromosome in population genetics
the x chromosome in population genetics

... the advent of practical DNA-sequencing technology: the first detailed sequence studies of the X chromosome appeared in 1997 and 1998 (REFS 3–6), and the first phylogenetic trees only in 1999 (REFS 7–9). Since then, X-chromosome-based studies have slowly accumulated; with the maturation of sequencing ...
PDF
PDF

... In annlyzing the data to asccrtain the number of mnjor gene pairs diffl'I'C'ntillting the pOl'ents, it WIlS ueC't'ssilry to set up a hypothesis as to th(' numher of gl.'lle puil's illyoh-cd and to detcrmine the pheno­ typt'S of the g!'notypes, the pl'llci.mnc('s of these phellotypes, tho PWPOl'tiOll ...
Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene
Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene

... Haiying Liu, Ning Li1, Cunling Jia2, Xiaoping Zhu and Zhihai Jia** College of Animal Science and Technology, China Agricultural University, Beijing, 100094, P. R. China ABSTRACT : The aim of the experiment was to detect polymorphisms in the keratin-associated protein 8.2 (KAP8.2) gene to determine a ...
Jeopardy - Southgate Schools
Jeopardy - Southgate Schools

... $100 Question from Other Crosses A cross between a black chicken(BB) with a white chicken (WW) produces all speckled offspring (BBWW). This type of inheritance is known as ...
Do gametes woo? Evidence for non-random unions at
Do gametes woo? Evidence for non-random unions at

... evidence, that the combination of egg and sperm at fertilization is largely independent of their genetic content. This equal transmission of alternative alleles through meiosis in heterozygotes ensures a balanced parental genetic contribution to offspring at each generation. Mendel’s First Law captu ...
Unit 1 Review Answer Key 1. Define the following terms: a
Unit 1 Review Answer Key 1. Define the following terms: a

... 20. If you were conducting a testcross with an unknown individual for one allele and you found the offspring to be 50% one phenotype and 50% the other, then what was the genotype of the unknown? A. Homozygous dominant B. Heterozygous C. Homozygous recessive D. Unknown based on this information 21. ...
PDF
PDF

... nucellar cell which acquires the developmental program of a functional megaspore, a mechanism referred to as apospory. Alternatively, if the embryo sac forms from a megaspore mother cell with suppressed or modified meiosis, the pathway is called diplospory (Fig. 20.2b). These two pathways, leading t ...
Chromosomal Microarray Analysis
Chromosomal Microarray Analysis

... Overview of CMA Examples of Common Findings Examples of Mosaicism Examples of Complex Abnormalities Examples of Small Copy Number Variants CMA Comprehensive-CMA plus SNPS Resolving Variants of Uncertain Significance Prenatal CMA Considerations Prenatal CMA Case Examples Types of Cancer Arrays ...
Azza Ahmed Ibrahim Abo senna_GST paper
Azza Ahmed Ibrahim Abo senna_GST paper

... 25% of AML cases were null in GSTT1 genotype compared with 20% of controls. Although this increase is minute, the role of GSTT1 null genotype in increasing the risk of AML cannot be neglected. Maybe, because of normal lower frequency of GSTT1 deletion polymorphism (20% in population), the number of ...
10.1 - My Haiku
10.1 - My Haiku

... between pairs of alleles long before the details of meiosis were known. Where Mendel states that pairs of alleles of a gene separate independently during gamete production, we can now attribute this to random orientation of chromosomes during metaphase I. Mendel made this deduction when working with ...
Genetic studies of psoriasis and psoriatic arthritis
Genetic studies of psoriasis and psoriatic arthritis

... transporters, SLC22A4 and SLC22A5. These results support the existence of a susceptibility region for psoriasis on chromosome 5q32, probably involved in the arthritic phenotype and not caused by the 3 SNPs within SLC22A4 and SLC22A5. Analysis of two candidate genes, CSTA and ZNF148, within the linka ...
Using the transcriptome to determine the genetic mechanisms of
Using the transcriptome to determine the genetic mechanisms of

... Joseph Powell Centre for Neurogenetics and Systems Genomics Winter School in Mathematical and Computational Biology ...
2. In vivo Maternal Haploid Induction in Maize
2. In vivo Maternal Haploid Induction in Maize

... chromosomes   from   the   donor   plant.   Low   frequency   of   haploids   and   changes   in   the   constitution   of   cytoplasm   from   the   donor   genotype   make   this   system   not   very   attractive   to   derive   inbred   l ...
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Quantitative trait locus

A quantitative trait locus (QTL) is a section of DNA (the locus) that correlates with variation in a phenotype (the quantitative trait). The QTL typically is linked to, or contains, the genes that control that phenotype. QTLs are mapped by identifying which molecular markers (such as SNPs or AFLPs) correlate with an observed trait. This is often an early step in identifying and sequencing the actual genes that cause the trait variation.Quantitative traits are phenotypes (characteristics) that vary in degree and can be attributed to polygenic effects, i.e., the product of two or more genes, and their environment.
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