Slide 1
... Use either this parameter or blastResult_url parameter as input but not both together. blastResult_url: url of the blast result. .[BLAST_report]. oldRefFile_direct_data: old blast result file..[BLAST_report]. Use either this parameter or oldblastResult_url as input but not both together. oldRefFile_ ...
... Use either this parameter or blastResult_url parameter as input but not both together. blastResult_url: url of the blast result. .[BLAST_report]. oldRefFile_direct_data: old blast result file..[BLAST_report]. Use either this parameter or oldblastResult_url as input but not both together. oldRefFile_ ...
Applied Animal Breeding and Gene
... of measurement used. Those character for which there are two or only relatively distinct categories are described as showing discrete variation. For other characters where the number of categories is large and limited to the units and accuracy of measurement used for classification, these characters ...
... of measurement used. Those character for which there are two or only relatively distinct categories are described as showing discrete variation. For other characters where the number of categories is large and limited to the units and accuracy of measurement used for classification, these characters ...
pdf
... not only because of the uncertain physiological role it plays in these organisms, which require oxygen to oxidize ammonia and generate energy (17), but also because it has been demonstrated that ammonia oxidizers, such as Nitrosomonas europaea, produce the environmentally important trace gases nitri ...
... not only because of the uncertain physiological role it plays in these organisms, which require oxygen to oxidize ammonia and generate energy (17), but also because it has been demonstrated that ammonia oxidizers, such as Nitrosomonas europaea, produce the environmentally important trace gases nitri ...
YY - Zanichelli online per la scuola
... Factors that influence evolution are: • mutations in gametes (that change the genetic pool); ...
... Factors that influence evolution are: • mutations in gametes (that change the genetic pool); ...
N. crassa et al. However, despite the speed and
... Physically unordered asci can be used to map centromeres in any chromosome of the complement if a recognizable marker is present at any one of the seven centromeres. This is because second-division segregation of a marker that is centromere-distal to a single exchange will result in asci that are te ...
... Physically unordered asci can be used to map centromeres in any chromosome of the complement if a recognizable marker is present at any one of the seven centromeres. This is because second-division segregation of a marker that is centromere-distal to a single exchange will result in asci that are te ...
poster_CSHL_2007
... FIRE (for Finding Informative Regulatory Elements) is a highly sensitive approach for motif discovery from expression data, based on mutual information. It has the following characteristics: ...
... FIRE (for Finding Informative Regulatory Elements) is a highly sensitive approach for motif discovery from expression data, based on mutual information. It has the following characteristics: ...
Guidance on the Use of Biochemical and Molecular Markers
... The GAIA distance component is computed with the GAIA software developed by GEVES. The GAIA distance is a combination of differences observed on phenotypic characteristics, where each difference contributes to the distance according to the reliability of the characteristics, especially regarding its ...
... The GAIA distance component is computed with the GAIA software developed by GEVES. The GAIA distance is a combination of differences observed on phenotypic characteristics, where each difference contributes to the distance according to the reliability of the characteristics, especially regarding its ...
Microarray-based comparative genomic hybridisation (array CGH)
... What are the advantages of array CGH? The main advantage of array CGH is the ability to explore all 46 chromosomes in a single test and to detect any DNA imbalance including extra or missing chromosomes and loss or gain of chromosome material much more precisely than conventional chromosome analyses ...
... What are the advantages of array CGH? The main advantage of array CGH is the ability to explore all 46 chromosomes in a single test and to detect any DNA imbalance including extra or missing chromosomes and loss or gain of chromosome material much more precisely than conventional chromosome analyses ...
Sequence Alignment - Bilkent University
... mutation is associated with breast cancer. The 80 kb genomic sequence of this gene is composed at 40% of Alu elements. ...
... mutation is associated with breast cancer. The 80 kb genomic sequence of this gene is composed at 40% of Alu elements. ...
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 ...
... 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 ...
important update on the status of curly calf syndrome
... to compare it to how a black Angus cow and a black Angus bull can produce a red calf. A dominant trait masks a recessive trait, so in the Angus world, black (dominant) masks red (recessive). What you see when you look at the animal is the “phenotype” – the physical characteristics – in our example t ...
... to compare it to how a black Angus cow and a black Angus bull can produce a red calf. A dominant trait masks a recessive trait, so in the Angus world, black (dominant) masks red (recessive). What you see when you look at the animal is the “phenotype” – the physical characteristics – in our example t ...
2. Primer Design
... screen are individual channels. Each of these can hold separate protein/DNA sequences. Click on the channel of interest to work with the sequence it contains). 3. Go to Restriction/Restriction Analysis. Here, you will be walked through a series of dialogues asking a variety of question about the sou ...
... screen are individual channels. Each of these can hold separate protein/DNA sequences. Click on the channel of interest to work with the sequence it contains). 3. Go to Restriction/Restriction Analysis. Here, you will be walked through a series of dialogues asking a variety of question about the sou ...
DNA Sequence Capture and Enrichment by Microarray Followed by
... management of massive amounts of data and potential interference from highly homologous sequences (e.g., pseudogenes) (10 ). Because the NGS technology is so new, QC of the sequence data (including the accuracy of reads, quality scores for reads, and sequencingcoverage needs) has not yet been well d ...
... management of massive amounts of data and potential interference from highly homologous sequences (e.g., pseudogenes) (10 ). Because the NGS technology is so new, QC of the sequence data (including the accuracy of reads, quality scores for reads, and sequencingcoverage needs) has not yet been well d ...
Chromosomal Microarray Analysis
... Chromosomal Microarray Analysis revealed an approximately 28.2 Mb LOSS in copy number in the distal and subtelomeric regions of the long arm of chromosome 18 suggestive of mosaicism. This deletion includes the critical region of chromosome 18q deletion syndrome (OMIM 601808). FISH analysis and parti ...
... Chromosomal Microarray Analysis revealed an approximately 28.2 Mb LOSS in copy number in the distal and subtelomeric regions of the long arm of chromosome 18 suggestive of mosaicism. This deletion includes the critical region of chromosome 18q deletion syndrome (OMIM 601808). FISH analysis and parti ...
Familial Aortopathy — Gene Panels
... and (reversible) terminator nucleotides labelled with fluorochromes specific to the nucleotide type. The sequencing reaction comprises a series of cycles that allows the successive addition of nucleotides that are detected at each cycle. The resulting sequences are assembled and compared with the re ...
... and (reversible) terminator nucleotides labelled with fluorochromes specific to the nucleotide type. The sequencing reaction comprises a series of cycles that allows the successive addition of nucleotides that are detected at each cycle. The resulting sequences are assembled and compared with the re ...
CF Overview of CF Genotypin and NSQAP services
... Sequenom® assays other than HerediT™ CF (MALDI-TOF Mass Spectrometry) ViennaLab Diagnostics GmbH CF StripAssay® ...
... Sequenom® assays other than HerediT™ CF (MALDI-TOF Mass Spectrometry) ViennaLab Diagnostics GmbH CF StripAssay® ...
Meiosis and mitosis - The Open University
... It is possible to follow a character, such as eye colour or hair colour in humans, that is handed down from generation to generation. Such characters are said to be inherited characters (or heritable characters) and are determined by genes. A gene can be considered as a unit of inheritance, which de ...
... It is possible to follow a character, such as eye colour or hair colour in humans, that is handed down from generation to generation. Such characters are said to be inherited characters (or heritable characters) and are determined by genes. A gene can be considered as a unit of inheritance, which de ...
Alternative Splicing
... splice sites (AG) are accessible to give two different mature mRNAs and therefore two different protein products (Protein Z and Protein Y). The splicing regulator (X) binds to a splice site which is located within a coding region of the pre-mRNA. This splice site is now no longer accessible to the s ...
... splice sites (AG) are accessible to give two different mature mRNAs and therefore two different protein products (Protein Z and Protein Y). The splicing regulator (X) binds to a splice site which is located within a coding region of the pre-mRNA. This splice site is now no longer accessible to the s ...
Digital PCR Analysis of Maternal Plasma for
... conditions in cases in which both parents carry the same mutation is more complex, because the majority of mutant alleles in plasma will be maternal in origin. Prenatal diagnosis with cffDNA in these circumstances requires the determination of allelic ratios (or RMD) in maternal plasma rather than t ...
... conditions in cases in which both parents carry the same mutation is more complex, because the majority of mutant alleles in plasma will be maternal in origin. Prenatal diagnosis with cffDNA in these circumstances requires the determination of allelic ratios (or RMD) in maternal plasma rather than t ...
DROSOPHILA: GENETICS MEETS BEHAVIOUR
... Behaviour, arguably one of the most complex phenotypes, has been considered to be the action of an animal in response to its internal and external environment. However, this definition of behaviour is vague and not limited to behavioural phenotypes. From an experimental point of view, each behaviour ...
... Behaviour, arguably one of the most complex phenotypes, has been considered to be the action of an animal in response to its internal and external environment. However, this definition of behaviour is vague and not limited to behavioural phenotypes. From an experimental point of view, each behaviour ...
GENETICS PROBLEM AP
... stripes (B). If an animal carries a dominant C but two recessive bb, pigment will be distributed evenly and the mouse will be black. If it carries two recessive cc, no pigment will be made and it will be white. If it carries a dominant C and a dominant B. it will be striped. The following cros ...
... stripes (B). If an animal carries a dominant C but two recessive bb, pigment will be distributed evenly and the mouse will be black. If it carries two recessive cc, no pigment will be made and it will be white. If it carries a dominant C and a dominant B. it will be striped. The following cros ...
Chapter 10: Sexual Reproduction and Genetics
... Real-World Reading Link Look around your biology class. You might notice ...
... Real-World Reading Link Look around your biology class. You might notice ...
BioACTS Quarter THREE
... scientists to learn from each other? Explain using examples from the discovery of DNA’s structure. ...
... scientists to learn from each other? Explain using examples from the discovery of DNA’s structure. ...
Genetics Tutorial
... The gene for flower color has two varieties: purple and white. These alternative forms of a gene are called alleles. The purple flower has two alleles that determine it's flower color. One allele came from each parent. We use capital letters to abbreviate the two dominant alleles (PP). The white flo ...
... The gene for flower color has two varieties: purple and white. These alternative forms of a gene are called alleles. The purple flower has two alleles that determine it's flower color. One allele came from each parent. We use capital letters to abbreviate the two dominant alleles (PP). The white flo ...
Population Genetics 2: Linkage disequilibrium Consider two loci and
... When r = 0.5 the loci are said to be un-linked; such loci are very far apart on the same chromosome, or in different chromosomes. When r < 0.5 the genes are said to be linked. When r =0 the loci are in permanent disequilibrium. ...
... When r = 0.5 the loci are said to be un-linked; such loci are very far apart on the same chromosome, or in different chromosomes. When r < 0.5 the genes are said to be linked. When r =0 the loci are in permanent disequilibrium. ...
Gene
A gene is a locus (or region) of DNA that encodes a functional RNA or protein product, and is the molecular unit of heredity. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic traits. Most biological traits are under the influence of polygenes (many different genes) as well as the gene–environment interactions. Some genetic traits are instantly visible, such as eye colour or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that comprise life.Genes can acquire mutations in their sequence, leading to different variants, known as alleles, in the population. These alleles encode slightly different versions of a protein, which cause different phenotype traits. Colloquial usage of the term ""having a gene"" (e.g., ""good genes,"" ""hair colour gene"") typically refers to having a different allele of the gene. Genes evolve due to natural selection or survival of the fittest of the alleles.The concept of a gene continues to be refined as new phenomena are discovered. For example, regulatory regions of a gene can be far removed from its coding regions, and coding regions can be split into several exons. Some viruses store their genome in RNA instead of DNA and some gene products are functional non-coding RNAs. Therefore, a broad, modern working definition of a gene is any discrete locus of heritable, genomic sequence which affect an organism's traits by being expressed as a functional product or by regulation of gene expression.