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文件擴展名查詢

.ab1 文件擴展名

開發商: N/A
文件類型: DNA Electropherogram File
你在這裡因為你有,有一個文件擴展名結尾的文件 .ab1. 文件與文件擴展名 .ab1 只能通過特定的應用程序推出。這有可能是 .ab1 文件是數據文件,而不是文件或媒體,這意味著他們並不是在所有觀看。

什麼是一 .ab1 文件?

存儲在文件中的內容.ab1擴展與支持科學機器和設備收集的DNA信息的科學數據。從對生物系統的科學分析開發相關的軟件程序的數據也可以存儲在這些AB1文件。 DNA的電泳圖的文件被更通常被稱為AB1文件。用於分析DNA鹼基序列和電泳信息的一些應用程序使用.ab1格式存儲原始數據。這些應用還可以用於創建,打開和查看這些AB1文件的內容。這些應用包括應用生物系統公司序列分析軟件應用程序,該程序BIOEDIT和Geospiza FinchTV版本基於Microsoft Windows的平台和Mac系統。這些程序,當安裝在兼容OS計算機運行,集成了這些AB1文件的支持。這些應用都大大有助於改善遺傳突破,因為當時的遺傳科學家和研究人員已經開始使用這些程序的開發。

如何打開 .ab1 文件?

推出 .ab1 文件,或者你的電腦上的任何其他文件,雙擊它。如果你的文件關聯的設置是否正確,這意味著應用程序來打開你的 .ab1 文件將其打開。這是可能的,你可能需要下載或購買正確的應用程序。這也有可能是你有正確的應用程序在PC上,但 .ab1 文件還沒有與它相關聯。在這種情況下,當您嘗試打開一個 .ab1 文件,你可以告訴Windows的應用程序是正確的該文件。從這時起,打開 .ab1 文件將打開正確的應用程序。 點擊這裡修復.ab1文件關聯錯誤

打開一個應用程序 .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,不要重命名擴展 .ab1 文件,或任何其他文件。這不會更改文件類型。只有特殊的轉換軟件可以從一個文件類型更改一個文件到另一個。

什麼是文件擴展名?

文件擴展名是一組三個或四個字符在文件名的末尾,在這種情況下, .ab1. 文件擴展名告訴你它是什麼類型的文件,並告訴Windows哪些程序可以打開它。窗戶經常關聯一個默認程序的每個文件的擴展名,這樣,當你雙擊該文件,程序會自動啟動。當該程序不再是您的PC上,有時可以得到一個錯誤,當您試圖打開相關的文件。
修復.ab1文件關聯錯誤

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