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Gaining biological specificity in gene set analysis by correcting for
Gaining biological specificity in gene set analysis by correcting for

...  Most results are based on ranking GO terms  Only small percentage is expected to be significant and relevant  Need to add similar comparisons considering only significant GO terms or comparing the actual p-values ...
Disability Theory in A Separate Peace
Disability Theory in A Separate Peace

... able-bodied future. First, I will argue that the vision of society as able-bodied explains why Gene “becomes” Finny gradually throughout the novel. To conclude I will contend that only “supercrips” are welcomed into our society. This will further explain why when Gene fully “absorbs” Finny, as theor ...
Gene conversion analysis of the mouse Pilr locus
Gene conversion analysis of the mouse Pilr locus

... Gene conversion has played a role in shaping the mouse Pilr locus and is detected by a variety of phylogenetic and statistical methods. Phylogenetic analysis of a conserved 3 kb region (the promoter through to intron 3) suggests that Pilrb1 and Pilrb2 are more related to each other than they are to ...
Targeting the Noncoding Genome with CRISPR
Targeting the Noncoding Genome with CRISPR

... sequencing to identify CRISPR-mutated loci enriched in the drug-exposed cells. The researchers isolated hundreds of loci—mostly in the 5’ ends of the target genes—that when mutated, decreased gene expression and validated that 24 of 25 loci surrounding CUL3 indeed resulted in reduced transcription a ...
Know Your Chromosomes - Indian Academy of Sciences
Know Your Chromosomes - Indian Academy of Sciences

... Antithrombin is an a-globulin protein found in the plasma. It acts as the principal inhibitor of thrombin and other coagulation factors in blood. Deficiency of AT3 leads to disorders related to inappropriate blood clotting like 'thrombophlebitis' and 'acute aortic thrombosis'. Patients die premature ...
Last semester I tried a new strategy to teach macro
Last semester I tried a new strategy to teach macro

... disaster, or out-migration, that wiped out part of the candy/gene pool, strategically, certain “genes” were lost, the variation within the pool decreased, which they could see, as well as the increase in variation between populations. The chart is projected the entire time, so they can connect what ...
Chromomere - aqinfo.com
Chromomere - aqinfo.com

...  Bead like projections – along entire length of polytene chromosome  Heavier stained than inter-chromomeric regions  Clear in dipteran salivary gland chromosome as dark bands  Genes are located within chromomere  One chromomere – single gene  Evidence – local coiling of continuous DNA thread ...
HoFH text summary
HoFH text summary

... Some individuals with FH have inherited a single copy of an FH disease-causing mutation from one of their parents, leading to “heterozygous” FH (HeFH). For others, both parents have passed on the FH mutation, which causes a more serious form of the disease, known as “homozygous” FH (HoFH).2–6 Patien ...
LBSC 708L Session 1
LBSC 708L Session 1

... The nirIX gene cluster of Paracoccus denitrificans is located between the nir and nor gene clusters encoding nitrite and nitric oxide reductases respectively. The NirI sequence corresponds to that of a membrane-bound protein with six transmembrane helices, a large periplasmic domain an ...
Ch06 Answers to Concept Check Questions
Ch06 Answers to Concept Check Questions

... Answer: Mitochondria need rRNA and tRNA genes to translate proteins within the mitochondrial matrix. FIGURE 6.8 Concept check: How have chloroplasts and mitochondria changed since the initial endosymbiosis events, which occurred hundreds of millions of years ago? Answer: Chloroplast and mitochondria ...
Dihybrid Punnett Squares
Dihybrid Punnett Squares

Workshop practical
Workshop practical

... Run the example API script to check everything is installed correctly: perl biomart-web/scripts/new_0_5_exampleSimple.pl ...
RNA gene prediction
RNA gene prediction

Supplemental Materials and Methods (doc 44K)
Supplemental Materials and Methods (doc 44K)

... (62°57'E, 67°03'N). The sampling area has a mean annual temperature of -5.8°C and a mean annual precipitation of 505 mm. Cryoturbated peat circles (4 to 25 m in diameter) which develop through soil mixing as a result of frost action, are located on a peat plateau containing thick, unturbated peat so ...
The BCM Microarray Core Facility
The BCM Microarray Core Facility

The “silent” noise of bacterial genes…
The “silent” noise of bacterial genes…

... Research scientists from INRA, AgroParisTech, CNRS, INSERM and the University of Montpellier have succeeded in observing the expression of bacterial genes with an unprecedented accuracy. Using fluorescence-based techniques and microscopy, the scientists were able to count the number of synthesized p ...
Gene Drives - WordPress.com
Gene Drives - WordPress.com

... Remaining issues with gene drives • CRISPR often cuts off target. • The gene drives must not reduce the reproductive fitness of the carrier animal. • Gene drives must be robust and stable enough to get through the entire population without mutations. This might require periodic release. • In mosqui ...
hox genes
hox genes

... vitripennis [6], Hox genes are organized in a contiguous, single-copy cluster in the leafcutter ant Atta cephalotes. However, only 9 of the 10 genes usually found in the cluster were identified here (Figure1). Despite sequence similarity analyses against the entire genome, a homolog for Hox3-A was n ...
Table S1: Description of the cohort used for the novel - HAL
Table S1: Description of the cohort used for the novel - HAL

... (http://evs.gs.washington.edu/EVS/). For whole genome sequencing, we used 54 individual genomes sequenced by Complete Genomics (www.completegenomics.com). For both methods, we observed a very low sequencing coverage of SHANK1 and SHANK3 (Figure S3). Whole genome sequencing seems to be a better appro ...
PPT - wFleaBase
PPT - wFleaBase

... Comment: -shorter protein is only 44.5378151260504 % of the original protein length. Insufficient. (FL_alt_splice_flag; 0) Stitched EST lacks compatibility with preexisting protein annotations; invalid and no alt-splice template available. Applied to Dappu1_FM5_196379,0 >asmbl_7600-based protein MSF ...
Genetic Modification Regulations and Procedures
Genetic Modification Regulations and Procedures

... Geneticists can use recombination data to map a chromosome’s genetic loci  One of Morgan’s students, Alfred Sturtevant, used crossing over of linked genes to develop a method for constructing a chromosome map.  This map is an ordered list of the genetic loci along a particular chromosome. Copyrig ...
FocalScan: Scanning for altered genes in cancer based on
FocalScan: Scanning for altered genes in cancer based on

... of doing this is through the calculation of a correlation coefficient between changes in copy number and RNA (5,6). This favors either a linear (in the case of the Pearson coefficient) or a general increasing/decreasing relationship (for instance the Spearman coefficient) between the two types of al ...
FROM SINGLE GENE TO PHENOTYPE: QUESTIONING A
FROM SINGLE GENE TO PHENOTYPE: QUESTIONING A

... fluidity of function in additional transcripts. However, a practical challenge remains; such a model of transcript function requires a flexible structural framework to allow for the quantification of the genetic effect. Many exceptions to traditional functionality are compounded by the inability of ...
Paper Baby Lab - Mrs. Wolodkowicz`s Biological Realm
Paper Baby Lab - Mrs. Wolodkowicz`s Biological Realm

... 1. Select 1 member of the team to represent the “mother” and the other member, the “father” (the 2 members will each be given a coin which will represent their genes being donated to their child. 2. First, the sex must be determined: The “father” only, will flip (heads=boy & tails=girl). Note determ ...
Genome duplication, divergent resolution and
Genome duplication, divergent resolution and

... and medaka have almost twice as many Hox clusters as, for example, humans. Additional evidence favouring the fish-specific genome duplication hypothesis comes from comparative mapping studies, which have identified a large number of mammalian genes with two zebrafish ‘co-orthologs’19–21. Furthermore ...
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Copy-number variation



Copy-number variations (CNVs)—a form of structural variation—are alterations of the DNA of a genome that results in the cell having an abnormal or, for certain genes, a normal variation in the number of copies of one or more sections of the DNA. CNVs correspond to relatively large regions of the genome that have been deleted (fewer than the normal number) or duplicated (more than the normal number) on certain chromosomes. For example, the chromosome that normally has sections in order as A-B-C-D might instead have sections A-B-C-C-D (a duplication of ""C"") or A-B-D (a deletion of ""C"").This variation accounts for roughly 13% of human genomic DNA and each variation may range from about one kilobase (1,000 nucleotide bases) to several megabases in size. CNVs contrast with single-nucleotide polymorphisms (SNPs), which affect only one single nucleotide base.
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