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文件扩展名查询

.ab1 文件扩展名

开发商: N/A
文件类型: DNA Electropherogram File
你在这里因为你有,有一个文件扩展名结尾的​​文件 .ab1. 文件与文件扩展名 .ab1 只能通过特定的应用程序推出。这有可能是 .ab1 文件是数据文件,而不是文件或媒体,这意味着他们并不是在所有观看。

什么是一 .ab1 文件?

存储在文件中的内容.ab1扩展与支持科学机器和设备收集的DNA信息的科学数据。从对生物系统的科学分析开发相关的软件程序的数据也可以存储在这些AB1文件。 DNA的电泳图的文件被更通常被称为AB1文件。用于分析DNA碱基序列和电泳信息的一些应用程序使用.ab1格式存储原始数据。这些应用还可以用于创建,打开和查看这些AB1文件的内容。这些应用包括应用生物系统公司序列分析软件应用程序,该程序BIOEDIT和Geospiza FinchTV版本基于Microsoft Windows的平台和Mac系统。这些程序,当安装在兼容OS计算机运行,集成了这些AB1文件的支持。这些应用都大大有助于改善遗传突破,因为当时的遗传科学家和研究人员已经开始使用这些程序的开发。

如何打开 .ab1 文件?

推出 .ab1 文件,或者你的电脑上的任何其他文件,双击它。如果你的文件关联的设置是否正确,这意味着应用程序来打开你的 .ab1 文件将其打开。这是可能的,你可能需要下载或购买正确的应用程序。这也有可能是你有正确的应用程序在PC上,但 .ab1 文件还没有与它相关联。在这种情况下,当您尝试打开一个 .ab1 文件,你可以告诉Windows的应用程序是正确的该文件。从这时起,打开 .ab1 文件将打开正确的应用程序。 点击这里修复.ab1文件关联错误

打开一个应用程序 .ab1 文件

Applied Biosystems EditView or 3100 Conversion Utility

Applied Biosystems EditView or 3100 Conversion Utility

The Conversion utility developed by Applied Biosystems is an efficient tool that helps DNA analyzing less time consuming. The sample file format from the Data Collection and data analyzing software versions 2.0 of the Applied Biosystems are not compatible with the older applications. Data collection and data analyzing software version 1.1 like the GeneScan and Genotyper are one of these older applications. They have a distinct color field in their plate records which the newer versions do not have. This distinct color field is where a diamond, which is required by GeneScan to measure the size of the DNA fragments, is placed into the cell equal to the dye color which is the standard size. The newer versions of the plate records do not have a column of color information where users can just copy the sample names and paste it into this field which will generate into the GeneScan and Genotyper sample information field. The GenoTyper software has allelic ladder samples running in Kazam macro has a sample info field where the word "ladder" is required to appear. It is possible to enter the diamond and sample info manually but then it will require so much time just to finish the task. conversion utility makes it easy by automatically placing the diamond and sample info into the sample files which enables the older versions of the software to work with the new ones.
Applied Biosystems Sequencing Analysis Software

Applied Biosystems Sequencing Analysis Software

Developed by Applied Biosystems, the Sequencing Analysis Software is made to edit, analyze, display, print and save sample files created from DNA analyzers by Apllied Biosystems and Genetic Analyzers by ABI PRISM. This software performs tasks such as Definition and displaying of mixed bases, calculation and displaying of quality values, calculation and displaying of clear range, calculation of sample score, creation of output files in ABI (.seq), FASTA (.seq), Phred (.phd.1) and standard chromatogram format (.scf). It also produces analysis reports which contains sample analysis statics and prints this reports, it also prints data for each sample file and if enabled, it makes an Audit Trail to keep track of all modifications made to bases and analysis. The concepts used in this software are as follows: Analysis Protocol, which has all the settings needed for analysis and applied in performing basecalling and post processing and the Analysis Report which demonstrates the data analysis status, the Clear Range, the Length of Read which is the measurement of the length of quality bases, the Quality Values (QVs) the estimate of basecalling accuracy, the Sample Score, the KB basecaller which is an algorithm that computes mixed or pure bases and quality values, and the ABI basecaller which identifies pure bases.
BioEdit

BioEdit

A biological sequence editor, BioEdit provide the basic functions needed for nucleic and protein sequence analysis, alignment, manipulation, and editing. It has a graphical interface for editing and sequence manipulation, with various editing options and it anchors alignment columns that helps in protecting fixed regions in alignment. This software can both automatically or manually annotate sequences using through features like exons, promoters and all other GenBank standard feature types. For synchronized hand alignment, BioEdit groups sequences into color-coded families and locks group members. It uses user-defined motif searching with the use of standard Prosite nomenclature which utilizes IUPAC characters to search for nucleic acid sequence, amino acid sequence, and text searches. It also has Rudimentary phylogenetic tree viewer that supports printing and node flipping, and RNA comparative analysis tools which includes potential pairings, covariation and mutual information analyses, and it also has amino acid translation which aligns protein-encoding nucleic acid sequences.
Geospiza FinchTV for Mac

Geospiza FinchTV for Mac

FinchTV is a genetics research program that lets you view DNA sequence traces on multiple platforms, view raw data and search for regular expressions. It recognizes popular chromatogram formats for you to read chromatogram files. It can display chromatogram traces in a multi-window or single window view. It can display above-the-trace quality values, DNA sequences and additional chromatogram information when available. You can print your all your traces in a single page or in multiple panels in a single page. You can export your DNA sequence to a FASTA text file format. You can edit, insert or delete your bases. You can copy and select sequence data for use on other programs. Save your edits into a new chromatogram file for future purpose. Use simple base queries or regular expressions to search for your data. You can view your raw data from AB1 files. Launch NCBI BLAST to perform searches. You can reverse traces and complement traces. FinchTV for Mac requires PPC, Mac OS X 10.2.8 or later. With the new version 1.4, you can use custom scale settings to print your traces. You can edit, view and save chromatogram files with vector masked regions and quality trimming from Geospiza Finch Suite. Update for interface of OS X 10.4 [Tiger] is available with the FinchTV 1.4.
CubicDesign DNA Baser

CubicDesign DNA Baser

CubicDesign DNA Baser is an application that deals specifically in the field of molecular biology. DNA sequence assembly, automatic sample processing, analysis of DNA sequence, mutation detection, format conversion and sample processing simulations are the CubicDesign DNA Baser’s capability. The user may customize the background, nucleotides and chromatograms. The software may suggest and correction in case of a vague base. And those unclear bases will be highlighted for proper notification. Assembly engine may also be personalized. DNA samples may be assembled and aligned to a referred sequence, import from ABI, SCF, SEQ, TXT, FASTA, GBK formats. Traces may be also viewed and edited, convert the output to Multi- FASTA and other mentioned formats. The metadata in the user's contigs may be integrated automatically, detect or remove the vectors. CubicDesign DNA Baser run in Windows and Mac specifically on this following hardware: 333MHz for the processor, 64 MB of RAM, 1024 x 768 screen resolution, 2 MB Hard Drive space.

提醒一句

要小心,不要重命名扩展 .ab1 文件,或任何其他文件。这不会更改文件类型。只有特殊的转换软件可以从一个文件类型更改一个文件到另一个。

什么是文件扩展名?

文件扩展名是一组三个或四个字符在文件名的末尾,在这种情况下, .ab1. 文件扩展名告诉你它是什么类型的文件,并告诉Windows哪些程序可以打开它。窗户经常关联一个默认程序的每个文件的扩展名,这样,当你双击该文件,程序会自动启动。当该程序不再是您的PC上,有时可以得到一个错误,当您试图打开相关的文件。
修复.ab1文件关联错误

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