Rapid Typing 5.4 Download ~UPD~

RapidTyping is a convenient and easy-to-use keyboard trainer that will help you improve your typing speed and reduce typos. With its lessons organized for various student level, RapidTyping will teach you touch typing or enhance existing skills.

Advance your typing speed and accuracy with the newest typing tutor! With Rapid Typing Tutor you will learn using your keyboard more efficiently in just a few easy lessons for absolutely free. Kids can learn by playing a typing game, while adults can take pre-configured courses or create their own training lessons. Rapid Typing Tutor is perfect for adults and kids, students and teachers, and provides comprehensive reporting and progress tracking for every student. Powerful statistics include 15 different parameters, including words-per-minute, characters-per-minute and accuracy reports.

Rapid Typing 5.4 Download

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The innovative typing tutor has a cheerful and intuitive user interface full of colors to make learning to type fun. The typing tutor features a variety of visual cues to help adults and kids master the computer keyboard, and provides full course statistics in tables and charts. Supporting multiple users makes Rapid Typing Tutor usable at schools, colleges and universities.

Secretaries, teachers and writers will find the ability of Rapid Typing Tutor to create their own courses custom-tailored to each student truly indispensible. Custom courses make it possible creating your own typing tutor meeting your own requirements. Whether you need to master a specific key, set of keys or a keyboard layout that you need to master, a custom-built typing tutor is your best solution.

The free typing tutor includes a full virtual keyboard with both hands moving over it to display the proper typing position for each hand and finger. Highlighted zones for each finger make placing your fingers correctly a second nature in no time.

For non-standard layout users, Rapid Typing Tutor automatically creates a new virtual keyboard based on the layout. You can take typing lessons for multiple keyboard layouts by quickly switching between them.

Although using a JIS keyboard posed a few early problems, I managed to set up colemak fairly easily on both Mac OS X and Linux. I have also been typing Japanese using colemak for Japanese input, but this hasn't been too good due to the poor placement of K and J. I will probably switch to one of the many alternative romaji based keyboard layouts after colemak gets comfortable.

# I don't plan on using kana input, as the JIS kana layout is actually also rather poor. I also don't like how kana input layouts (including the tens of alternate layouts) end up either using 4 rows, or overuse the shift key.

I wish there were a typing test that would give you a graph of instantaneous typing speed so I could see what I am peaking at. It's frustrating to be cruising along and then make a mistake and in the attempt to correct it my fingers spatz out and I take so long to recover that I end up with 35-40 WPM rating.

true...but the problem with the peak typing speed is that when you actually type, you do make mistakes which you have to fix and you don't type at your peak speed but at your average speed during your typing span. Thus, the most accurate speed is the average.

To me, peak speeds are pretty much useless. I can of course devise a test that gives me a "typing speed" to match Ms. Blackburn more or less, but what's the point? I'd only be lulling myself into false confidence and produce results that don't compare to anything interesting really. The thing I like with the TypingMaster test is that it seems to report something related to how fast I can actually type a long text. And that's what I need to do in real life, not excel at the arstneioarstneioarstneio race track.

As an educational material, RapidTyping combines animated backgrounds and a brightly colored interface to teach users touch typing or the technique of typing words without the need to look at the keyboard every so often. This is an important skill for writers, programmers, encoders, and the like.

Randomly amplified polymorphic DNA (RAPD) has been used for rapid typing of Lactobacillus plantarum strains. RAPD was used with either purified chromosomal DNA serving as template in the polymerase chain reaction, or with crude cell extracts, and using a 9-mer primer with 80% G+C content. Amplified DNA was visualized by ethidium bromide staining after separation on agarose gels. Patterns from 20 Lact. plantarum strains and two Lact. pentosus strains were analysed using the Pearson products moment correlation coefficient (r) and the unweighted pair group method with arithmetic averages (UPGMA). With some exceptions, the two sources of template DNA gave the same clusters and subclusters of strains at the similarity level of 50%. About 50% of the strains could be individually separated from all the other tested strains. The buffer brand, the amount of primer and crude cell extract used in the PCR-step were crucial for the final pattern.

Coxiella burnetii has the potential to cause serious disease and is highly prevalent in the environment. Despite this, epidemiological data are sparse and isolate collections are typically small, rare, and difficult to share among laboratories as this pathogen is governed by select agent rules and fastidious to culture. With the advent of whole genome sequencing, some of this knowledge gap has been overcome by the development of genotyping schemes, however many of these methods are cumbersome and not readily transferable between institutions. As comparisons of the few existing collections can dramatically increase our knowledge of the evolution and phylogeography of the species, we aimed to facilitate such comparisons by extracting SNP signatures from past genotyping efforts and then incorporated these signatures into assays that quickly and easily define genotypes and phylogenetic groups. We found 91 polymorphisms (SNPs and indels) among multispacer sequence typing (MST) loci and designed 14 SNP-based assays that could be used to type samples based on previously established phylogenetic groups. These assays are rapid, inexpensive, real-time PCR assays whose results are unambiguous. Data from these assays allowed us to assign 43 previously untyped isolates to established genotypes and genomic groups. Furthermore, genotyping results based on assays from the signatures provided here are easily transferred between institutions, readily interpreted phylogenetically and simple to adapt to new genotyping technologies.

Sequence based DNA signatures are widely used for molecular typing as they provide unambiguous results that are easily transferred and compared between labs. In this era of rapid and inexpensive sequencing, whole genome sequence comparisons often reveal many polymorphisms that can be used to develop new assays for increased discrimination among samples and to better define phylogenetic relatedness. Despite drastic reductions in cost, whole genome sequencing is still expensive relative to other typing technologies. As well, the data handling, processing, and interpretation required for whole genome sequence analyses make sub-genome typing methods more viable when many samples need processing. For phylogenetic and population genetic inferences, a large sample size is also important as samples are compared to each other and accuracy of conclusions is directly tied to comprehensive sampling. Unfortunately, switching to new typing methods often results in lost information between old and new systems as data cannot be directly compared. As such, past data and efforts may be simply discarded or, when possible, old samples may be re-analyzed with the new typing scheme (for example, see [1]). Ideally, new signatures or assays should not only be transferrable between labs, but also enable newly typed samples to be directly compared to existing collections. For Coxiella burnetii, it is particularly important to compare typing results to other collections as C. burnetii collections are rare, sparse and not easily transferred due to select agent regulations and biosecurity concerns. In order to better understand epidemiological patterns we have therefore built upon an existing sequence based typing scheme to produce a few simple and rapid assays whose results are unambiguous, easily transferrable, and can be directly compared to the largest characterized collection of C. burnetii in the world.

Despite the serious nature of Q fever, little is known about the prevalence and dissemination patterns of C. burnetii. Most genotyping methods are cumbersome and require relatively large quantities of DNA. Before the very recent development of a cell-free growth procedure [6], propagation required cell tissue culture or proliferation in embryonated eggs. Even with this significant improvement, culturing still requires a select agent facility, considerable expertise, and is a slow process. Thus, in the rare instances where a case of Q fever is identified, it is not likely that a sample will be successfully cultured and genotyped. Therefore, tools that facilitate the comparison of isolates or field-collected strains are particularly important.

We developed genotyping assays based on 14 SNPs. Twelve SNPs that define the major clades were used to develop Melt-MAMA assays (Table 1) as described by Vogler et al. [14]. Briefly, the melt-MAMA design utilizes allele-specific mismatch amplification mutation assay primers [15] coupled with GC- or T-rich primer tails. These tails force allele specific melt properties for PCR amplicons, allowing allelic differentiation via melt curve analysis. Two other SNPs from MST allele comparisons were used to develop TaqMan minor groove binding dual-probe assays according to Easterday et al. [16] (Table 2) and to illustrate that multiple SNP-interrogation methods can be used to assay SNP signatures. 17dc91bb1f