Re: Install Bowtie Windows

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Francis Caya

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Jul 14, 2024, 2:23:45 PM7/14/24
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I'm trying to develop a GUI in python for analyze tRNA-Seq data which could be run in Linux and Windows. For this it is needed run some programs like: bowtie2, samtools or bedtools, which can be downloaded by anaconda easily on Linux but is a headache on Windows. This programs can't be downloaded on Windows so I had to install Windows Subsystem for Linux (WSL) and tried to downloaded by this way.

I tried to install bowtie with the source code (installed previosly MinGW-W64 and MSYS) but I got several error messages - it says my machine is not 64 bit. I modified the MakeFile with notepad. Run make and g make, nut nothing has worked.I have also tried to install Bowtie2 with mingw64.zip but also there nothing.

Install Bowtie Windows


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This is anecdotal evidence but in the past I have found that Windows "home" editions are missing some system level features that result in strange messages/inability to run certain commercial bioinformatics programs (Vector NTI was one). Issues you noted with MinGW may be related to this. You should consider upgrading the home edition to pro, if you want to stick with Windows. That would allow you to install Windows subsystem for Linux (bash). Without this ability, Windows for bioinformatics analysis is going to prove limiting.

I have pretty much no background in programming or anything like that, so I don't exactly know how to make my own binary from source code. Also, I'm pretty sure that windows 10 does not come with a command bar. Can anyone help?

Use Bowtie Chart by MAQ Software to quickly compare values in one or more categories. Bowtie Chart by MAQ Software is ideal for displaying sales metrics, such as the flow of a sale from channel to category. The thickness of the bowtie's branches indicates the relative weight of each category. Create a full bowtie to showcase how a cumulative value splits into two distinct sub-categories. Alternately, you can create a half bowtie, showcasing the distribution of data within a source.

This package provides an R wrapper of the popular bowtie2 sequencing reads aligner and AdapterRemoval, a convenient tool for rapid adapter trimming, identification, and read merging. The package contains wrapper functions that allow for genome indexing and alignment to those indexes. The package also allows for the creation of .bam files via Rsamtools.

This is a result of having a licensing mechanism without a central server. Not having a central licensing server has advantages and disadvantages. Having to deploy new codes is a disadvantage as it takes more work. Not having to install a license server, adjusting firewalls, and having trouble with people going off the network is an advantage.

If you want to also deploy the dat license file you might need to capture changes to create a deployment script, or manually make sure the dat file is placed next to the exe. Another option is for end-users to enter it manually. Note that BowTieXP has no dependencies other than having the .NET Framework 4.0 (Full Profile) or higher installed. Deployment is xcopy deployment; all the msi does is:

BowTieXP (version 9.0 and higher), requires the .NET Framework 4.0 (Full Profile) or higher to be installed. Windows 8 and later come with a new enough version already installed out of the box. On Windows Vista and 7, you need to do this manually, if not yet already installed.

In order to run different versions of BowTieXP side by side, all we have to do is to download the different versions we want and make sure to grab the versions for manual installation (the zip files).

In the first case (msi installed), BowTieXP will download the msi and ask windows to install it, upgrading the old installation. Windows will ask for admin credentials if the current user is not an administrator.

In the second case (installed from zip file), BowTieXP will download the new exe and replace the current one. If the user has no write access to the exe no attempt will be made (i.e. the update check is notification only, auto-upgrade is not possible).

You may wonder if you can analyze your NGS data on your own computer, not by accessing TACC's lonestar or GSAF's fourierseq server. Answer is definitely yes! However, a problem is that bwa, bowtie, samtools, and many utilities cannot be installed on Windows OS. If you are a Mac user or linux is already installed on your computer, please skip this page.

There are multiple ways.
First, install a linux-like system (ex. Cygwin). Cygwin is a collection of tools which provide a Linux look and feel environment for Windows. Visit Cygwin, download it, and use Cygwin terminal like you used in TACC's lonestar server. But Cygwin is not a way to run native Linux apps on Windows. Linux-like system is not linux per se. You may need to install additional modules and commands on Cygwin in order to complete certain jobs.

Second option is to install a virtual machine (VM) and linux. VM is a completely isolated guest operating system installation within a normal host operating system. VM allows you to have two or more OS in one physical PC machine. You can install linux, OS X, Windows Vista, Windows 98 on a VM. Which VM and linux is the best? Actually, there is no best choice because everyone has own taste. In terms of popularity, Oracle VM Virtual Box and Ubuntu is a pretty nice choice. More importantly, they are free! I won't explain how to install VM and Ubuntu on your Windows because you can easily find wonderful instructions by googling. Google "virtual box ubuntu". Here is one easy and useful guide.

Ubuntu inside VB and Windows work like two different computers in one physical PC. When you generate beautiful graphs and awesome tables on Ubuntu for your labmeeting, you can't open it with MS office on Windows. Don't send them to yourself via email. Shared Folders functionality makes multiple OS to share some space in the hard drive. You can run NGS utilities on your Ubuntu and spit out the output into the shared folder. Then, open it with MS office on your Windows. Oh! before you set up Shared Folders, you should install the Guest Additions on your VM. Here is how to install Guest Additions and how to share folders

Providing system wide access to miRge3.0, cutadapt, bowtie and bowtie-build, please type or (copy and paste) and submit each of the following commands on the terminal:
NOTE: Make sure to change your path to python bin folder; Replace /home/arun/.local/ with /Path on your computer/.

Mac comes with python2.7 installed by default. To use python3.7, creating an alias in .bash_profile would do the trick
Open a new terminal window. Use vim editor if you are familiar using this editor vi .bash_profile or open the .bash_profile using text editor by open -e .bash_profile and add the following line at the bottom of the text.

Providing system wide access to miRge3.0, cutadapt, bowtie and bowtie-build, please type or (copy and paste) and submit each of the following commands on the terminal:
NOTE: Make sure to change your path to python bin folder; Replace /Users/loaneruser/Library/ with /Path on your computer/.

Once installed, run the plugin by selecting your reads and reference sequence then clicking on Align/Assemble - Map to Reference in the toolbar. Bowtie is available as an option in the Algorithm drop-down menu.

I am installing a series of programs for bioinformatics purposes; I am installing the folders of these packages in /usr/local/lib/ and creating soft links to the executable files in /usr/bin/ so I am expecting to have them visible in the environment. But when I type the executables in the terminal, the commands are not recognized, so they are not in the environment.

So bash (I suppose you're using bash, but many shells will work like this) will look for the executable in the current directory, not in PATH.To add /usr/local/lib/Bowtie to PATH, just edit /.bashrc and add export PATH=$PATH:/usr/local/lib/Bowtie. This way bash will look for bowtie2 in this directory.

Before aligning reads, bowtie2 index should be build. refs is a character vector of fasta reference file paths. A prefix of bowtie index should be set to argument bt2Index. Then, 6 index files with .bt2 file name extension will be created with bt2Index prefix.

The variable reads_1 and reads_1 are preprocessed reads file paths. With bowtie2 index, reads will be mapped to reference by calling bowtie2. The result is saved in a sam file whose path is set to output

Flexible flashing products are tenaciously sticky, so before installing the first piece over the sill, I draw a plumb line on the sheathing. This way I can line up the edge of the flashing, and know that it will run parallel with the sill.

There are a lot of pieces of flashing to install, but the idea is always the same: Like installing house wrap or siding, you always work in layers from the bottom up when flashing. Now we can move on to one of the more fun part of the job, trimming the door.

Unzip the contents of this file to a directory where you would like the software to be (e.g. C:\SpliceSeq). NOTE: If you have a previous version of SpliceSeq Viewer, please install the new version into a new directory or delete the old version if installing to the same directory. To run SpliceSeq Viewer, double click on SpliceSeq.jar or open a Dos/Unix window, cd to the directory where you unpacked the application and run:

SpliceSeq Analyzer is included in the local installation package and does not need a separate installation step. However, SpliceSeq Analyzer relies on an external alignment program Bowtie, which should be installed and configured as described in the next section.

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