ProSeq, or "Processor of sequences" is a tiny program designed to handle DNA sequence data. This program is dedicated to people that work in the medical or scientific environment and need a tool that can keep up with their processes.
ProSeq's purpose is to facilitate routine work regarding the preparation of DNA
sequence polymorphism datasets, from the very first steps of checking sequence chromatograms to the final stages of testing the dataset before the analysis and preparing input files for many DNA polymorphism analysis programs.
The application includes an internal database that links sequences to individuals and individuals to populations, simplifying handling and analysis of datasets containing multiple genes. This database aids the users in making an idea about the connections between different specific DNA strains about their ethnicity and location.
Regarding the UI functionality, three viewing modes allows its users to sequences, polymorphisms in the alignment and the functional regions assigned to the chain. This allows for greater visibility regarding the graphical form of the sequences.
To sum it up, ProSeq is a professional tool aimed at a select base of users. IF you are studying DNA or work with it, you can give it a try, as you may find it useful in any given situations.
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ProSeq Crack Download For PC [2022-Latest]
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DNA data is processed via a series of viewing modes that allow to track the overview of the data. The information displayed is then saved to a database that tracks the origin of the DNA sample and allows to easily locate it when analyzing further datasets of a given origin.
Features:
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* NEW: View Mode
* NEW: View Mode
* Filter polymorphisms that match selected patterns
* Compute from a set of GenBank sequences as a file containing the resulting records
* Sequence alignment visualization from a pairwise BLAST output file
* Easy access of alignments to all stored DNA sequences
* Compute from a set of GenBank sequences as a file containing the resulting records
* Pairwise BLAST output file storage
* Easy access of alignments to all stored DNA sequences
* Combine all stored alignments to a file containing a result for each match in a column
* Compute Fasta from any number of DNA sequences in a pairwise BLAST output file
* Pairwise BLAST output file storage
* Combine all stored alignments to a file containing a result for each match in a column
* Display of the alignment of the “SELECT” sequence in Chromatogram view
* Display of the alignment of the “SELECT” sequence in a per-position alignment display
* Database and visualization of chains
* Database and visualization of the user chosen chromosomes
* Excel export of the database and chromosomes
* Simple batching of a user’s polymorphisms in order to reduce the time spent looking for a given polymorphism in a significant set of polymorphisms
* Retain the names of the populations in the final output
* Excel export of the database and chosen chromosomes
* Compute Fasta from a user’s input of DNA sequences in a pairwise BLAST output file
* Multiple sequence comparison of a user’s sequences to any number of user-selected sequences
* Works with a pairwise BLAST result file containing all the sequences used
* Works with a Fasta formatted result file
* Works with a pairwise BLAST result file containing all the sequences used
* Submit genes for a target investigation to GeneBank
* Export data to Excel
* Native support of polymorphisms
* Native support of unidirectional sequences
* Synchronization of data automatically
* Help files
* Documentation files
* Two main desktops: MacOS and Windows
* Links to the Internet and the GenBank database
* Storage of polymorphisms and individuals
* Er
ProSeq Crack
===========
Official website:
License:
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This program is distributed under GPL v3.0 license. The license is attached as part of the download.
Authors:
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Igor Staryk
Supporting:
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Igor Staryk
Change Log:
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17-May-2013
– The data is compressed with gzip before transmitting, saving ~10-15% of bandwidth (FTP transfer time).
– Added export to TIFF format
– Improved the look and feel
– Added a few examples
16-Apr-2013
– Minor update:
– Corrected a problem with the tree
– Code cleanup
– Fixed minor bugs
9-Apr-2013
– New interface
– Support of polymorphisms in the multiple sequences alignment
– Initial interface for importing polymorphism data with PYTHON and PERL
– Fixed bug in the update sequence function
– Added help
5-Jan-2013
– Fixed bug with the interface
– Fixed bug in some sequences
– Changed the handle of html tags
19-Nov-2012
– Fixed bug with setting the project
– Changed the folder structure
– Fixed bug in the C-E program
18-Oct-2012
– Fixed bugs in the functions.
17-Oct-2012
– Fixed bug with the manual display of the sequences
– Changed the double click action
– Support for variable sequence names
1-Aug-2012
– Improved input form in the C-E program
29-Jun-2012
– Added option to show only records with a specific sign on the polymorphism test
– Added polymorphism test analysis for the CPK sequence
12-Jun-2012
– Added double click action to the sequences display
– Fixed bug with new polymorphisms display
– Added a server
05-Jun-2012
– Added support for new polymorphisms display
25-May-2012
– Added option for a polymutations test
14-May-2012
– Changed the name of polymorphism frames
– Changed the color for the multiple sequences display
– Added possibility to display more information for aligned sequences
– Added calculation of a percentage and its display
– Added option to save results
– Added
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ProSeq Crack + Product Key Free
– Working with sequence data, including checking the chromosome and detecting duplications.
– Checking the alignment to check the presence of probable errors.
– Analyzing the sequences present in the alignment.
– Viewing the polymorphisms in an alignment.
– Viewing the polymorphisms in a given region.
– Viewing the population data at the level of individuals and populations.
– Analyzing the population data with regard to the origin of samples and populations.
– Viewing the data in the FASTA format or other specified formats.
– Viewing the data within a specific range of chromosome and coordinate in the database (optional).
– Viewing the data about the specific region and/or one or multiple sequences at once.
– Viewing sequences in the format custom.
– Viewing sequences in various dimensions.
– Viewing details about the sequence.
– Checking the type of the sequence.
– Creating a BED file for the sequences in a specific range of the chromosome.
– Creating a BED file for the polymorphisms in a specific range of the chromosome.
– Creating a BED file for the specific region in a specific range of the chromosome.
– Analyzing gene variants.
– Viewing the polymorphisms that match with a specific criteria.
– Viewing the locations where the polymorphism was identified and the type of the polymorphism.
– Analyzing the polymorphisms in a specific range of the polymorphism table.
– Browsing the results.
– Seeding sequences directly from the FASTA file.
– Seeding sequences directly from the sequences in the database.
– Exporting a specific polymorphism as a CSV file.
– Creating a custom format for the polymorphisms in a specific region.
– Creating a custom format for the polymorphisms in a specific range of the polymorphisms.
– Checking the specific polymorphisms for obvious errors.
– Reorganizing the polymorphisms in the polymorphisms table.
– Searching for a given sequence in the database.
– Searching for the specific polymorphisms in the polymorphisms table.
– Exporting the results as a CSV file.
– Exporting the results as a BED file.
– Analyzing the sequences related to a set of populations.
– Analyzing the sequences according to the geographical location of the individuals.
– Analyzing the sequences according to the ethnicity of the individual.
– Analyzing the sequences according to the geographical location of
What’s New In ProSeq?
2.1 Tool over complexity
ProSeq is a large and professional tool aimed at a select base of users. IF you are studying DNA or work with it, you can give it a try, as you may find it useful in any given situations.
In its case, we welcome all users who want to work on DNA related. But, of course, the tool is aimed to a select base of people with some knowledge of how DNA analysis works.
2.2 User experience
ProSeq is aimed at simplifying the work of users that are preparing their DNA polymorphism data. In a ‘normal’ DNA sequencing environment, we need to do several steps to prepare and work with the data.
We already discuss the advantages and problems of such a process in the About tab, if you want more information on that topic, we invite you to read the various pages.
2.3 Problem difficulty
ProSeq’s functions should be understood as a recipe in order to be able to use it for preparing each type of dataset.
Sometimes, doing the same things twice or more, or doing the same things twice with slight variations, is considered as the same work. In such case, ProSeq can help to save time and simplify the process of obtaining and organizing your results.
Important Note:
ProSeq’s functions and the user interface are not labeled in any way, in order to avoid the use of abbreviations, which should be avoided in DNA polymorphism databases. If in doubt, or if you need to learn more on a specific tool, we invite you to read the about tab.
We also recommend that you know at least a little bit about DNA sequencing before using this tool, as we have examples of possible cases.
For example, after DNA sequencing the material, we can find the sequences in a file with a specific name. We can then separate them by chromosome in order to prepare the data on the chromosome.
We can also separate them in each chain in order to prepare the data on it. This last step will require the identification of the chain link, which is managed by the user, the link identification being defined in a file included with ProSeq.
Then we have different cases of checking if we have all the sequences. In the first example, we don’t need to do anything. In the second example, we can do different actions depending on the number of chromosomes, and so on. In all cases, the first step is very important in the preparation of the
System Requirements:
Playable on most computers, tablets, and phones.
Overview
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