如何将纸上文字或文章段落快速输入到电脑.docx

如何将纸上文字快速输入到电脑在工作学习中，我们常常要将纸上有用的文字快速输入到电脑中，如何做到轻而易举不费吹灰之力将纸上有用的文字快速输入到电脑中？其实不难，下面小编带你见证奇迹的一刻（亲！需要的话认真保存好哦，以防不时之需！！！）幕前准备： 条件 1： 电脑一台、数码相机一台（具有高像素摄像头的也可，我试过了：可用，但就是乱码比较多，毕竟我的像素不高因此像素越高越好，你懂的！）条件 2： Word2003 版本以上 （别人用 Word2003 试验的，我用 Word2007 试验的另外，金山办公软件 WPS 应该也可以）doPDF （用于制作 PDF 文件） CAJViewer 软件（相信写过论文的都知道） 具体操作步骤如下： 步骤一： 安装 doPDF 和 CAJViewer 软件步骤二： 用相机或把需要的段落拍下来（网上截图也可以） 下面我以一篇英文片段为例（相机拍摄的，本来是老师要求我们翻译这些内容的，当时不知道有这个一条捷径，害得我们好苦，你懂的！）步骤三： 在 Word 文档中插入如上照片步骤四: 点击 Word 文件菜单（word2007 直接点击 ）→打印→在打印机选项中选择doPDF→确定 →浏览→选择存放位置和给文件命名（最好保存在桌面以防丢失）→保存→确定（此刻照片已经成功导入 PDF 文件） 。

如下演示一样：5、注意电脑是否已自动打开上述步骤获得的 PDF 文件（注意：一定要由 CAJViewer 打开该文件， Adobe Reader 打开无效，其他的软件没试过），若没打开，自己动手打开CAJViewer 软件，然后打开刚刚转换的 PDF 文件6、点击 CAJViewer 中的“文字识别”按钮 ,然后拖动鼠标画出需要“识别”的段落 7、点击 “发送到 WPS/Word(W)”按钮→发送到新建文档（插入当前光标位置），就换成 Word 文件了保存即可，此时可以任意编辑附：经上述步骤获得的内容：（注意：有可能出现乱码，谨记注意核对一下）DNA DAMAGE AND REPAFRmutant was isolated, techniques had not yet been developed for carrying outgenetic analysis with E. toll strain B. Thus, similar mutants in the more geneti-tally accessible E. toll K12 strain were sought. The search for mutants made useof the phenomenon of host-cell reactivation described earlier. Several hundredthousand cells of a mutagenized sample of E. toll were spread on agar along withabout tw a vaauea 1-t pnage. one concentration or gr}age on the plate was sucnthat before colonies became visible, each microcolony had been infected withseveral UV killed phage. If the microcolony consisted of wild-type cells, a frac-lion of the UV killed phage was reactivated, and these went on to infect and lysethe microcolony. Colonies of mutants unable to engage in host-cell reactivationwere also infected, but they did not release progeny phage and hence survivedto produce visible colonies. These colonies were streaked on agar to isolate themutant cell from free 户 age and wild-type cells (see Chapter 4), bacterial cul-lures were prepared, and the radiosensitivity of the cultures was tested. Many ofthese colonies were exceedingly sensitive to UVComplementation tests showed that the mutations fell into three classes,which defined the genes uvrA, uvrB, and uvrC. Biochemical analysis showedthat the uvrA, uvrB, anduvrC mutants are defective in an endonuclease requiredfor excision of thymine dimers (as well as in repair of many 帅 es of chemicaldamage). Survival curves for some of these mutants are shown in Figure 9-9. Sev-eral other classes of mutants were also found to be W sensitive.In studies of genetic recombination in E. toll (described in Chapter 14),which were totally unrelated to the repair phenomenon, recombination-deficientmutants were isolated. These mutations mapped in 山 ree genes, designated recA,recB, and recC. When the phenotypes of the rec mutants were examined, it wasdiscovered that they are sensitive to W radiation (see Figure 9-9). Biochemicalanalysis, however, showed that these mutants excised thymine dieters normally,indicating that a system that uses recombination (or at least requires the rec genes jis responsible for another type of repair.In the course of stu 如 ng DNA replication in E. toll, a mutation was isolatedin the gene polA, which encodes DNA Pol I. The mutant was viable, which sug-Bested that Pol I is not the major replication enzyme. This 助面 g provided theimpetus for seeking other DNA polymerases in E. toll, and in fact Pol III wasisolated from the polA mutant. Detailed examination of the polA mutant ulti-mately showed that it retained normal S'”3' exonuclease activity and had aresidual polymerizing activity of about 2% of the wild-type, which was sufficientfor it to play its essential role in the removal of RNA primers and the joining ofprecursor fragments (see Chapter 8). An important observation about the polAphenotype was that the mutant had somewhat increased sensitivity to UV, sug-Besting that DNA Pol I might be involved in DNA repair.切记：输出的文字一定要校对呀 ！因为有乱码！！！。