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ppt - Chair of Computational Biology
ppt - Chair of Computational Biology

... Eukaryotic genomes Transcription of protein-encoding regions is initiated at specific promoter sequences, and followed by removal of noncoding sequence (introns) from pre-mRNA by a splicing mechanism. 3 types of posttranscriptional events influence the translation of mRNA into protein and the accur ...
Using articles to explain possible causes of genetic
Using articles to explain possible causes of genetic

... jaw relative to head size, stiffness of joints, hip dislocations and severe, progressive cardiovascular disease 5. An interesting fact you learned ESR  The condition gets its name from the green work “geras” which means age  It's thought to affect 4 million newborns worldwide  Newborns normally a ...
1 X chromosome crossover formation and genome stability in
1 X chromosome crossover formation and genome stability in

... xnd-1(ok709); LG IV, ced-3(n717); LG V, mys-1(n3681), him-5(ok1896). Some strains were provided by the Caenorhabditis Genetics Center. xnd-1(ok709) was outcrossed multiple times for these studies due to long-term maintenance problems of the strain. Double and triple mutants were generated using sta ...
What is an Epigenetic Mechanism and why is it
What is an Epigenetic Mechanism and why is it

... Epigenetics & Music Use the Same Markings Andrea Baccarelli – Laboratory of Environmental Epigenetics ...
C2005/F2401 `07 -- Lecture 19 -- Last Edited
C2005/F2401 `07 -- Lecture 19 -- Last Edited

... 1. Chromosomes. DNA (+ associated proteins) visible in microscope as individual structures called chromosomes. DNA tightly coiled, easy to distribute but not accessible to enzymes of replic. and transc. (condensed > 10,000 X). Individual balls of string (in this state) vs unwound, tangled mess (betw ...
MICROBIAL GENETICS-III UGc - E
MICROBIAL GENETICS-III UGc - E

... Linear strands of DNA will almost always have a free 5′ phosphate group at one end and a free 3′ hydroxyl group at the other. Therefore, every DNA molecule has an intrinsic directionality. 5′ pGpTpCpCpApT—OH 3′ Where the phosphates are indicated by “p.” Levene’s early studies indicated that all four ...
Gene Section FANCC (Fanconi anaemia complementation group C) Atlas of Genetics and Cytogenetics
Gene Section FANCC (Fanconi anaemia complementation group C) Atlas of Genetics and Cytogenetics

... C; it represents about 15% of FA cases. Disease Fanconi anaemia is a chromosome instability syndrome/cancer prone disease (at risk of leukaemia). Prognosis Fanconi anaemia's prognosis is poor; mean survival is 16 years: patients die of bone marrow failure (infections, haemorrhages), leukaemia, or an ...
Supplementary data
Supplementary data

... Table ST2 shows all mutations present in cases analysed in this study, ordered by their position from 5’- to 3’- in the gene (amino acid position is given relative to the initiator methionine of the MECP2e2 isoform, as used in most previous reports). Mutations found in Glasgow as part of this study ...
1st set of Journal Clubs this Wednesday!
1st set of Journal Clubs this Wednesday!

... something causes it to be released.’ Positive control: ‘An activator causes the accelerator pedal to be pushed.’ Cis-acting sequence: Can only function if on same piece of DNA that its regulating Trans-acting factor: A gene product that can act in ‘trans’ i.e. diffuse to a location at a distance fro ...
bio genetics review guide - Google Docs
bio genetics review guide - Google Docs

... The  whole  of  the  genetic  information  of  an  organism   gene  mutation   a  change  in  the  base  sequence  of  a  gene.   Base  substitution   The  smallest  possible  change  is  when  one  base  in  a  gene  is  replaced ...
Phylogenetic Portrait of the Saccharomyces cerevisiae Functional
Phylogenetic Portrait of the Saccharomyces cerevisiae Functional

... GO-Slim analysis GO analysis was performed using the GO-Slim Mapper tool implemented in the Saccharomyces Genome Database (http://yeastgenome. org/cgi-bin/GO/goSlimMapper.pl). GO-Slim Mapper was used rather than standard GO Term finder because of the smaller, less redundant number of ontology terms u ...
grade 12 life sciences learner notes
grade 12 life sciences learner notes

Using the Basic Local Alignment Search Tool (BLAST) - bio-bio-1
Using the Basic Local Alignment Search Tool (BLAST) - bio-bio-1

DNA copy number analysis by MAPH: molecular diagnostic
DNA copy number analysis by MAPH: molecular diagnostic

... locus at a chromosome end, is shown as a peak. The first sam- BRCA1 or subtelomeric DNA analysis, however, the exon or ple is a heterozygous deletion of 17q (17q-) and the second is chromosome end that varies, if any, is not known. This can be an unbalanced translocation between chromosomes 16 and 3 ...
Cloning and characterization of a gene coding for a hydrophobin Fv
Cloning and characterization of a gene coding for a hydrophobin Fv

... Hydrophobins are composed of four loops, which are formed by disulfide bonds among eight cysteine residues that are highly conserved. Hydrophobins are grouped into two classes (classes I and II) due to their solubility in various solvents (Wessels 2000). All reported hydrophobins from basidiomycetes ...
Comparative Bacterial Genomics Genome Databases
Comparative Bacterial Genomics Genome Databases

PowerPoint
PowerPoint

... Promoter; terminator; structural genes; operator Copyright ©The McGraw-Hill Companies, Inc. Permission required for reproduction or display ...
Generation of the chromosome sequences
Generation of the chromosome sequences

... the gap and were not included in the gene set. For gi9507164, although the gap still exists in the May, 2004, release, we have extended sequence into that gap and can now account for all exonic sequence. Based on placements of mRNAs against chromosome 2 and 4, only one possible deletion was detected ...
Contextual Genetic Algorithms: Evolving Developmental Rules
Contextual Genetic Algorithms: Evolving Developmental Rules

... the concentrations of different proteins obtained may be selected accordingly, and thus evolve a system which is able to respond to environmental changes without changes in the major part of its genetic information (genome size optimization). One gene, different contexts, different proteins. This ma ...
Motifs and motif prediction methods I - BIDD
Motifs and motif prediction methods I - BIDD

LP - Columbia University
LP - Columbia University

... Both sexes have 22 pairs of chromosomes that look the same regardless of sex, but the 23rd pair is not the same in both sexes. In females, the 23rd pair consists of 2 large chromosomes that look alike. In males the 23rd pair consists of a large and a small chromosome that do not look alike but act ...
uk national collaborative usher study
uk national collaborative usher study

... Changes in the DNA sequence are called variants. Variants can be pathogenic or they could be neutral (this is when they would be called polymorphisms). Q. What is haplotype analysis? Haplotype analysis is a test to identify sections of DNA that are similar to each other. Q. What is a genotype? A gen ...
Introduction to the GCG Wisconsin Package
Introduction to the GCG Wisconsin Package

... HS (cont. resulting alignment) ...
Introduction to the GCG Wisconsin Package
Introduction to the GCG Wisconsin Package

The vertebrate genome annotation (Vega) database
The vertebrate genome annotation (Vega) database

... (NMD) Further more, transcript variants for which a CDS cannot be assigned confidently, are classified into the following main types: (i) Transcript: does not qualify for any of the specific types below. (ii) Retained intron: relative to an appropriate reference variant, transcript contains intronic se ...
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Non-coding DNA

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