 
									
								
									Motifs and motif prediction methods I - BIDD
									
... sequences •Able to detect distant relationships with only few well conserved residues ...
                        	... sequences •Able to detect distant relationships with only few well conserved residues ...
									Genomic Organization of Evolutionarily Correlated Genes in
									
... The need for efficient molecular interplay in time and space within a cell imposes strong constraints that could be partially relaxed if relative gene positions along chromosomes were appropriate. Comparative genomics studies have demonstrated the short-scale conservation of gene proximity along bact ...
                        	... The need for efficient molecular interplay in time and space within a cell imposes strong constraints that could be partially relaxed if relative gene positions along chromosomes were appropriate. Comparative genomics studies have demonstrated the short-scale conservation of gene proximity along bact ...
									Evolutionary Genomics of Fast Evolving Tunicates
									
... way to genome compaction in O. dioica is that the majority of genes contain very small introns. In fact, most introns are very short, being on average less than 50 nt in length, and only 2.4% of them are larger than 1 kb (Denoeud et al. 2010). Still, some genes have relatively large introns and inte ...
                        	... way to genome compaction in O. dioica is that the majority of genes contain very small introns. In fact, most introns are very short, being on average less than 50 nt in length, and only 2.4% of them are larger than 1 kb (Denoeud et al. 2010). Still, some genes have relatively large introns and inte ...
									2 Identifying Conserved Elements in the Toxin Sensor and
									
... 2.5 What is Bioinformatics? During the last 15 years one of the greatest breakthroughs in biochemistry was the emergence of bioinformatics. Bioinformatics uses the power of computer science to analyze biology data and generate new information. This new field of life sciences has emerged, because (1) ...
                        	... 2.5 What is Bioinformatics? During the last 15 years one of the greatest breakthroughs in biochemistry was the emergence of bioinformatics. Bioinformatics uses the power of computer science to analyze biology data and generate new information. This new field of life sciences has emerged, because (1) ...
									NIH Public Access
									
... Pleiotropy and epistasis were first described in the early 20th century to explain observed deviations in Mendelian inheritance patterns. German zoologist and geneticist Ludwig Plate defined pleiotropy in 1910 as one mutation resulting in multiple, independent phenotypes. For example, in Waardenburg ...
                        	... Pleiotropy and epistasis were first described in the early 20th century to explain observed deviations in Mendelian inheritance patterns. German zoologist and geneticist Ludwig Plate defined pleiotropy in 1910 as one mutation resulting in multiple, independent phenotypes. For example, in Waardenburg ...
									Day 1. General aspects for genetic map construction
									
... sequences combination using PE or small size MP ...
                        	... sequences combination using PE or small size MP ...
									Narrow-Sense Heritability
									
... has, the greater their potential for growing tall  Additive alleles behave something like alleles that result in incomplete dominance  More CR alleles results in F2 Generation ...
                        	... has, the greater their potential for growing tall  Additive alleles behave something like alleles that result in incomplete dominance  More CR alleles results in F2 Generation ...
									Torch 13.2 (April 2012)
									
... Is there a test for the MYD88 L265P mutation? Whole genome sequencing requires lots of purified DNA. For many patients with WM, obtaining such amounts is problematic. In addition, whole genome sequencing can take 4-6 months and, at present, can cost $5,000 per genome (down considerably from $100,00 ...
                        	... Is there a test for the MYD88 L265P mutation? Whole genome sequencing requires lots of purified DNA. For many patients with WM, obtaining such amounts is problematic. In addition, whole genome sequencing can take 4-6 months and, at present, can cost $5,000 per genome (down considerably from $100,00 ...
									Concepts and relevance of genome
									
... is a sequence of more than three billion DNA bases that can be represented by one of four letters: A, C, G or T. Much of the genome sequence is identical or highly conserved across the human population, but every person’s genome is unique. A given person’s genome sequence is likely to differ from th ...
                        	... is a sequence of more than three billion DNA bases that can be represented by one of four letters: A, C, G or T. Much of the genome sequence is identical or highly conserved across the human population, but every person’s genome is unique. A given person’s genome sequence is likely to differ from th ...
									anterior olfactory nucleus (aon) - Dashboard
									
... Internal: widespread, medium density and intensity; External: widespread, scatteredmedium density low intensity Internal: widespread, medium density and intensity; External: widespread, scatteredmedium density low intensity Internal: widespread; medium-high density, medium-low intensity; External: s ...
                        	... Internal: widespread, medium density and intensity; External: widespread, scatteredmedium density low intensity Internal: widespread, medium density and intensity; External: widespread, scatteredmedium density low intensity Internal: widespread; medium-high density, medium-low intensity; External: s ...
									Biochemistry Lecture 23 THE LAST ONE!
									
... • DNA is template for codes, but not direct template – DNA transcr’d  mRNA ...
                        	... • DNA is template for codes, but not direct template – DNA transcr’d  mRNA ...
									Conflicting Phylogenies for Early Land Plants are Caused by
									
... The problem underlying the conflict in many of these studies can be viewed as a question of where to place the charophyte root on a tree consisting of (in sequence) liverworts–mosses–hornworts–tracheophytes. If the root is placed between hornworts and tracheophytes then bryophytes will be monophyleti ...
                        	... The problem underlying the conflict in many of these studies can be viewed as a question of where to place the charophyte root on a tree consisting of (in sequence) liverworts–mosses–hornworts–tracheophytes. If the root is placed between hornworts and tracheophytes then bryophytes will be monophyleti ...
									Quantitative Genetics
									
... has, the greater their potential for growing tall Additive alleles behave something like alleles that result in incomplete dominance More CR alleles results in F2 Generation ...
                        	... has, the greater their potential for growing tall Additive alleles behave something like alleles that result in incomplete dominance More CR alleles results in F2 Generation ...
									Detection of cystic fibrosis transmembrane conductance regulator
									
... analysis of the CFTR gene using varied screening methods, a number of cases remain unsolved and could be attributable to the presence of large gene rearrangements, as recently shown for CF patients. METHODS: We carried out a complete CFTR gene study in a group of 222 CBAVD patients with strict diagn ...
                        	... analysis of the CFTR gene using varied screening methods, a number of cases remain unsolved and could be attributable to the presence of large gene rearrangements, as recently shown for CF patients. METHODS: We carried out a complete CFTR gene study in a group of 222 CBAVD patients with strict diagn ...
									Genome position and gene amplification | SpringerLink
									
... site. We note that because DHFR is the target of methotrexate, exposure to the drug should inhibit synthesis of thymidylate and reduce levels of thymidine-based nucleotides. Such a reduction in nucleotide levels could cause DNA damage; however, the concentrations used here are not expected to do so ...
                        	... site. We note that because DHFR is the target of methotrexate, exposure to the drug should inhibit synthesis of thymidylate and reduce levels of thymidine-based nucleotides. Such a reduction in nucleotide levels could cause DNA damage; however, the concentrations used here are not expected to do so ...
									Molecular mechanisms of sex determination and evolution of
									
... are highly enriched for repetitive DNA and transposable elements and often heterochromatic to a large extent. This peculiar genetic organization of the Y is certainly a derived character. It is logical to postulate that the pair of sex chromosomes at the initial stage of its evolution was, like any ...
                        	... are highly enriched for repetitive DNA and transposable elements and often heterochromatic to a large extent. This peculiar genetic organization of the Y is certainly a derived character. It is logical to postulate that the pair of sex chromosomes at the initial stage of its evolution was, like any ...
									Letter The Evolution of Male–Female Sexual
									
... model for the evolution of anisogamy/oogamy from isogamous mating types (Charlesworth 1978). If this model applies to MAT3, then the degree of differentiation between MAT3 alleles from each mating type in isogamous species should be much lower than in males–females from anisogamous and oogamous spec ...
                        	... model for the evolution of anisogamy/oogamy from isogamous mating types (Charlesworth 1978). If this model applies to MAT3, then the degree of differentiation between MAT3 alleles from each mating type in isogamous species should be much lower than in males–females from anisogamous and oogamous spec ...
									Lecture 16 Notes CH.15
									
... The Chromosomal Basis for Inheritance: Sex-linked genes exhibit unique patterns of inheritance 15.2 Although female mammals inherit two X chromosomes, only one X chromosome is active X-Inactivation in Female Mammals In mammalian females, one of the two X chromosomes in each cell is randomly inactiv ...
                        	... The Chromosomal Basis for Inheritance: Sex-linked genes exhibit unique patterns of inheritance 15.2 Although female mammals inherit two X chromosomes, only one X chromosome is active X-Inactivation in Female Mammals In mammalian females, one of the two X chromosomes in each cell is randomly inactiv ...
									Genomic scars as biomarkers of homologous recombination
									
... of which contribute to the conservative homologous recombination repair of DNA double-strand breaks. Nonetheless, several setbacks in clinical trial settings have highlighted some of the issues surrounding the investigation of PARP inhibitors, especially the identification of patients who stand to b ...
                        	... of which contribute to the conservative homologous recombination repair of DNA double-strand breaks. Nonetheless, several setbacks in clinical trial settings have highlighted some of the issues surrounding the investigation of PARP inhibitors, especially the identification of patients who stand to b ...
									A single nucleotide polymorphism of the TNRC9 gene associated
									
... Breast cancer is a multifactorial disease. Environment, genetics, and immunological defects are major factors in the etiology of breast cancer (Parkin et al., 2005). It has been reported that close relatives of patients have an approximately 2-fold increased risk of cancer, and the genetic factors b ...
                        	... Breast cancer is a multifactorial disease. Environment, genetics, and immunological defects are major factors in the etiology of breast cancer (Parkin et al., 2005). It has been reported that close relatives of patients have an approximately 2-fold increased risk of cancer, and the genetic factors b ...
									Introduction_to_Human_Genetics
									
... – When the allele has a complete loss of function it is often called an amorphic mutation Leaky mutations: – If some function may remain, but not at the level of the wild type allele The degree to which the function is lost can vary ...
                        	... – When the allele has a complete loss of function it is often called an amorphic mutation Leaky mutations: – If some function may remain, but not at the level of the wild type allele The degree to which the function is lost can vary ...
									Nature Genetics: doi:10.1038/ng.3791
									
... overlapping 26 bp reads). These shortened reads were mapped to the dm3 reference genome and the number of reads starting at each position was counted for each line. From this alignment map, a Universal Mappability Map (UMM) was created by considering genomic positions for which each DGRP line contai ...
                        	... overlapping 26 bp reads). These shortened reads were mapped to the dm3 reference genome and the number of reads starting at each position was counted for each line. From this alignment map, a Universal Mappability Map (UMM) was created by considering genomic positions for which each DGRP line contai ...
									Slide 1
									
... Genotypes that exhibit both genes as identical are called homozygous or purebred. Examples of homozygous genotypes would be BB or bb. BB would represent a homozygous dominant genotype while bb would represent a homozygous recessive genotype. Genotypes that exhibit genes that are not identical are c ...
                        	... Genotypes that exhibit both genes as identical are called homozygous or purebred. Examples of homozygous genotypes would be BB or bb. BB would represent a homozygous dominant genotype while bb would represent a homozygous recessive genotype. Genotypes that exhibit genes that are not identical are c ...
RNA-Seq
 
                        RNA-seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), is a technology that uses the capabilities of next-generation sequencing to reveal a snapshot of RNA presence and quantity from a genome at a given moment in time.
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									