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File Extension Søg

.ab1 File Extension

Udvikler: N/A
Filtype: DNA Electropherogram File
Du er her, fordi du har en fil, der har filtypenavnet slutter i .ab1. Filer med filtypen .ab1 kan kun blive lanceret af visse programmer. Det er muligt, at .ab1 filer er datafiler snarere end dokumenter eller medier, hvilket betyder, at de er ikke beregnet til at blive set på alle.

hvad er en .ab1 fil?

Indholdet gemmes i filer med .ab1 udvidelse er videnskabelige data med DNA detaljer indsamlet fra understøttede videnskabelige maskiner og udstyr. Data fra tilknyttede programmer udviklet til videnskabelig analyse af biosystemer kan også gemmes i disse AB1 filer. DNA elektroferogram filer er mere almindeligt benævnt AB1 filer. Nogle programmer, der anvendes til at analysere DNA basesekvens og elektroferogram information bruge .ab1 format til at gemme rådata. Disse programmer kan også bruges til at oprette, åbne og se indholdet af disse AB1 filer. Nogle af disse programmer omfatter Applied Biosystems Sequencing Analysis Software ansøgningen, BioEdit programmet og Geospiza FinchTV version til Microsoft Windows-baserede platforme og Mac-systemer. Disse programmer, når den er monteret i en computer med på en kompatibel OS, integrerer støtte til disse AB1 filer. Disse applikationer har i høj grad været med i udviklingen af ​​forbedrede genetiske gennembrud siden tidspunktet genetiske videnskabsfolk og forskere er begyndt at bruge disse programmer.

hvordan man åbner en .ab1 fil?

Iværksættelse af en .ab1 fil, eller enhver anden fil på din PC, ved at dobbeltklikke på det. Hvis din fil foreninger er indstillet korrekt, at det program, der er beregnet åbne din .ab1 fil vil åbne den. Det er muligt, du kan få brug for at hente eller købe den korrekte anvendelse. Det er også muligt, at du har det rigtige program på din pc, men .ab1 filer endnu ikke er forbundet med det. I dette tilfælde, når du forsøger at åbne en .ab1 fil, kan du fortælle Windows, hvilket program er det rigtige for den pågældende fil. Fra da af, åbner en .ab1 fil vil åbne den korrekte anvendelse. Klik her for at lave .ab1 filtilknytning fejl

applikationer, der åbner en .ab1 fil

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.

et ord af advarsel

Vær omhyggelig med ikke at omdøbe udvidelse på .ab1 filer eller andre filer. Dette vil ikke ændre filtypen. Kun speciel konvertering software kan ændre en fil fra én fil til en anden.

hvad er en fil forlængelse?

En fil udvidelse er det sæt af tre eller fire tegn i slutningen af ​​et filnavn, i dette tilfælde, .ab1. Filtypenavne fortælle dig, hvilken type fil det er, og fortælle Windows, hvilke programmer kan åbne den. Windows ofte knytter en standard program til hver filtype, så når du dobbeltklikker på filen, starter programmet automatisk. Når dette program er ikke længere på din pc, kan du nogle gange få en fejl, når du forsøger at åbne den tilknyttede fil.
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