M-protein and other intrinsic virulence factors of Streptococcus
... tes present a bidirectional replication starting from the origin of replication and reading in both directions until reaching a terminus (replication inset). The bidirectional replication therefore defines a leading and a lagging strand in the double helix. In the contrary, nucleotide sequence readi ...
... tes present a bidirectional replication starting from the origin of replication and reading in both directions until reaching a terminus (replication inset). The bidirectional replication therefore defines a leading and a lagging strand in the double helix. In the contrary, nucleotide sequence readi ...
BMC Genomics
... tes present a bidirectional replication starting from the origin of replication and reading in both directions until reaching a terminus (replication inset). The bidirectional replication therefore defines a leading and a lagging strand in the double helix. In the contrary, nucleotide sequence readi ...
... tes present a bidirectional replication starting from the origin of replication and reading in both directions until reaching a terminus (replication inset). The bidirectional replication therefore defines a leading and a lagging strand in the double helix. In the contrary, nucleotide sequence readi ...
The Non-LTR Retrotransposon Rex3 from the Fish Xiphophorus is
... teleost species and was found in the promoter region and in introns of various genes. To our knowledge, Rex3 is the first autonomous retrotransposon described to date which is widespread in teleosts. This wide distribution and occasional association with coding sequences may confer on Rex3 a predisp ...
... teleost species and was found in the promoter region and in introns of various genes. To our knowledge, Rex3 is the first autonomous retrotransposon described to date which is widespread in teleosts. This wide distribution and occasional association with coding sequences may confer on Rex3 a predisp ...
PDF
... determining the success of transgene stabilization. Modern fullgenomic sequencing technologies will likely assist the search for suitable endonucleases and allow for screening of mutations in loci that could be affected by endonuclease action. Results from a recently launched interlaboratory project ...
... determining the success of transgene stabilization. Modern fullgenomic sequencing technologies will likely assist the search for suitable endonucleases and allow for screening of mutations in loci that could be affected by endonuclease action. Results from a recently launched interlaboratory project ...
Additional file 5
... only in the Bp22 hybridization. Y-axis : Probe abundance (log2 scale). X-axis : Hybridization ratios of probes. “Common” probes correspond to probes exhibiting true signals (>2 SD) in both strains (purple), while probes exhibiting true signals in one strain and not the other were considered as “stra ...
... only in the Bp22 hybridization. Y-axis : Probe abundance (log2 scale). X-axis : Hybridization ratios of probes. “Common” probes correspond to probes exhibiting true signals (>2 SD) in both strains (purple), while probes exhibiting true signals in one strain and not the other were considered as “stra ...
"Using Model Organism Databases (MODs)". In: Current - SGD-Wiki
... “Model organisms” are nonhuman organisms that are typically used for biological research. The resulting data can be used as a framework for the interpretation and understanding of similar data from humans or other medically or economically important species. Popular model organisms include budding y ...
... “Model organisms” are nonhuman organisms that are typically used for biological research. The resulting data can be used as a framework for the interpretation and understanding of similar data from humans or other medically or economically important species. Popular model organisms include budding y ...
repetitive extragenic palindromic sequences in pseudomonas
... suggest that genome fragments lacking REP sequences could be pointing to regions recently acquired from other organisms and REP sequences could be a new tracer for getting insight into the key aspects of bacterial genome evolution, especially for studying pathogenicity acquisition. In addition, as t ...
... suggest that genome fragments lacking REP sequences could be pointing to regions recently acquired from other organisms and REP sequences could be a new tracer for getting insight into the key aspects of bacterial genome evolution, especially for studying pathogenicity acquisition. In addition, as t ...
Community Genome Annotation Training
... Introduction: There are several examples of successful creation/organization of knowledge by larger community rather than individual experts (for example, FoldIt – protein folding game http://fold.it/portal/ ; Wikipedia – reported to have fewer errors than Encyclopedia Britannica). We will try to cr ...
... Introduction: There are several examples of successful creation/organization of knowledge by larger community rather than individual experts (for example, FoldIt – protein folding game http://fold.it/portal/ ; Wikipedia – reported to have fewer errors than Encyclopedia Britannica). We will try to cr ...
genetic mapping and dna sequencing of the loblolly pine genome
... difficult than in most crops. The goal of this paper is to review the research on genetic mapping and gene sequencing on loblolly pine conducted at the Institute of Forest Genetics during the last five years. The review is not meant to be comprehensive for loblolly pine; much has been published by S ...
... difficult than in most crops. The goal of this paper is to review the research on genetic mapping and gene sequencing on loblolly pine conducted at the Institute of Forest Genetics during the last five years. The review is not meant to be comprehensive for loblolly pine; much has been published by S ...
#2
... regional variations of GC-content (the isochores), but the substitution processes at the origin of this structure are poorly understood. We have analyzed the pattern of neutral substitutions in 14.3 Mb of primate noncoding regions. We show that the GC-content toward which sequences are evolving is s ...
... regional variations of GC-content (the isochores), but the substitution processes at the origin of this structure are poorly understood. We have analyzed the pattern of neutral substitutions in 14.3 Mb of primate noncoding regions. We show that the GC-content toward which sequences are evolving is s ...
Transposable elements, genes and recombination in a 215
... a genome designated Am that is closely related to the genome of T. urartu, the A genome donor for tetraploid and hexaploid wheats. The large genome of T. monococcum (1C =5600 Mb; Bennett and Leitch 1995) is approximately 12 times larger than the genome of rice and 40 times larger than the genome of ...
... a genome designated Am that is closely related to the genome of T. urartu, the A genome donor for tetraploid and hexaploid wheats. The large genome of T. monococcum (1C =5600 Mb; Bennett and Leitch 1995) is approximately 12 times larger than the genome of rice and 40 times larger than the genome of ...
Final_peer-reviewed_manuscript - Research Explorer
... Clinton, former president of the United States and Tony Blair, former prime minister of the United Kingdom (through video conferencing), Francis Collins, director of the Human Genome Project and Craig Venter, CEO of Celera Genomics (published in Venter et al. 2001).13 Completion of the draft map was ...
... Clinton, former president of the United States and Tony Blair, former prime minister of the United Kingdom (through video conferencing), Francis Collins, director of the Human Genome Project and Craig Venter, CEO of Celera Genomics (published in Venter et al. 2001).13 Completion of the draft map was ...
Bioinformatics Dr. Víctor Treviño Pabellón Tec
... the contribution of tht alignment to the msa. For example, if an extra copy of one of the sequences is added to the alignment project, then for sequence pairs that do not include that sequence will increase, indicating a lesser role because the contributions of that pair have been out-voted by the a ...
... the contribution of tht alignment to the msa. For example, if an extra copy of one of the sequences is added to the alignment project, then for sequence pairs that do not include that sequence will increase, indicating a lesser role because the contributions of that pair have been out-voted by the a ...
New Perspectives on Rickettsial Evolution from New
... A wide variety of repetitive sequence elements are found in bacteria. These range from duplicated genes which exhibit varying degrees of homology like the ATP/ADP translocase genes, proline-betaine transporters, and sca gene families in Rickettsia, to the small palindromic repeat elements which are ...
... A wide variety of repetitive sequence elements are found in bacteria. These range from duplicated genes which exhibit varying degrees of homology like the ATP/ADP translocase genes, proline-betaine transporters, and sca gene families in Rickettsia, to the small palindromic repeat elements which are ...
Slides
... Mapping Structural Variation in Humans >1 kb segments - Structural Variations are Common 40% of the genome -Structural Variations are involved in phenotype variation and disease - Until recently most methods for detection were low resolution (>50 kb) ...
... Mapping Structural Variation in Humans >1 kb segments - Structural Variations are Common 40% of the genome -Structural Variations are involved in phenotype variation and disease - Until recently most methods for detection were low resolution (>50 kb) ...
Slide 1
... • Is it possible to define CNE boundaries better than with pairwise sequence alignment of Fugu and human? ...
... • Is it possible to define CNE boundaries better than with pairwise sequence alignment of Fugu and human? ...
Syllabus
... edition of Alberts is also available on line at pub med. You can search the text using terms such as chromosomes, mitosis, meiosis. For each lecture one or more review articles will be posted on line at bspace. You will be given guidance as to what to emphasis in your readings. Discussion: We will r ...
... edition of Alberts is also available on line at pub med. You can search the text using terms such as chromosomes, mitosis, meiosis. For each lecture one or more review articles will be posted on line at bspace. You will be given guidance as to what to emphasis in your readings. Discussion: We will r ...
ISMB2008PosterManagingGenomicData
... Dave Clements1, Hilmar Lapp1, Brian Osborne2, Todd J. Vision1 1National ...
... Dave Clements1, Hilmar Lapp1, Brian Osborne2, Todd J. Vision1 1National ...
Enlis Genome Research - Release Notes
... symbols to known official HGNC gene symbols, or warn if a gene symbol was not found - Gene Categories tool: Added "Disease Genes - CGD" default custom category. A category based on genes found in the Clinical Genomic Database (http://research.nhgri.nih.gov/CGD/) Useful for searching in the Variation ...
... symbols to known official HGNC gene symbols, or warn if a gene symbol was not found - Gene Categories tool: Added "Disease Genes - CGD" default custom category. A category based on genes found in the Clinical Genomic Database (http://research.nhgri.nih.gov/CGD/) Useful for searching in the Variation ...
Evidence for massive gene exchange between archaeal and
... of bacterial proteins that could be included into the conserved archaeal families was essentially uniform at the level of about 20% of each of the bacterial proteomes, with a sharp deviation at 39% observed for Aquifex (Table 3). Given these indications of a direct relationship between a sizeable fr ...
... of bacterial proteins that could be included into the conserved archaeal families was essentially uniform at the level of about 20% of each of the bacterial proteomes, with a sharp deviation at 39% observed for Aquifex (Table 3). Given these indications of a direct relationship between a sizeable fr ...
Reference genome sequence of the model plant Setaria
... family (Supplementary Fig. 3). The data indicate a very recent burst of LTR retrotransposon amplification, peaking within the last few hundred thousand years, whereas the LINE and CACTA elements exhibit a broader range of activity over the last 6 million years. Helitron elements seem to have undergo ...
... family (Supplementary Fig. 3). The data indicate a very recent burst of LTR retrotransposon amplification, peaking within the last few hundred thousand years, whereas the LINE and CACTA elements exhibit a broader range of activity over the last 6 million years. Helitron elements seem to have undergo ...
Attachment PDF Icon
... • The maximal genomic span of a PET genomic alignment must be less than one million bp ...
... • The maximal genomic span of a PET genomic alignment must be less than one million bp ...
Overview of splicing relevant databases - Stamm
... biological impact of alternative transcripts has created a high demand for tools enabling the identification, classification, functional annotation and expression profiling of alternative transcripts To meet this demand, several alternative splicing databases have been developed based on large-scale ...
... biological impact of alternative transcripts has created a high demand for tools enabling the identification, classification, functional annotation and expression profiling of alternative transcripts To meet this demand, several alternative splicing databases have been developed based on large-scale ...
Human Genome Project
The Human Genome Project (HGP) is an international scientific research project with the goal of determining the sequence of chemical base pairs which make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and functional standpoint. It remains the world's largest collaborative biological project. The project was proposed and funded by the US government; planning started in 1984, got underway in 1990, and was declared complete in 2003. A parallel project was conducted outside of government by the Celera Corporation, or Celera Genomics, which was formally launched in 1998. Most of the government-sponsored sequencing was performed in twenty universities and research centers in the United States, the United Kingdom, Japan, France, Germany, and China.The Human Genome Project originally aimed to map the nucleotides contained in a human haploid reference genome (more than three billion). The ""genome"" of any given individual is unique; mapping ""the human genome"" involves sequencing multiple variations of each gene.