Abhimanyu Singh
A bioinformatics beginner
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Libraries or management tools for high throughput sequencing data
Last updated 611 days ago by LEGEGATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.These methods enable the analysis of data sets of any size on multi-core desktop...Jarvis’ laboratory
Dr. Jarvis’ laboratory studies the neurobiology of vocal communication. We want to know how the brain generates, perceives, and learns behavior. We use vocal communication as a model behavior. Emphasis is placed on the molecular pathways involved in...-
My commonly used commands in Bioinformatics
Last updated 2873 days ago by Rahul NayakFYI, I've found it useful to use MUMmer to extract the specific changes that Racon makes, so I can evaluate them individually: minimap -t 24 assembly.fasta long_reads.fastq.gz | racon -t 24 long_reads.fastq.gz - assembly.fasta... Professor and Associate Professors (PB-IV) Assistant Professors (PB-III) Job at IIIT, Allahabad
Indian Institute of Information Technology, Allahabad Devghat, Jhalwa, Allahabad – 211012, Uttar Pradesh, India E-mail: contact@iiita.ac.in, faculty.applications@iiita.ac.in Web: www.iiita.ac.in Phone : 0532-2922031/27/67 Applications are...NanoPack: visualizing and processing long-read sequencing data
By Jit 2720 days agogithub.com - The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible...-
Find certain files/documents in Linux OS
Last updated 4444 days ago by Rahul NayakAs bioinformatician I know the fact that we usually handle the large dataset and lost in the huge numbers of files and folders. In order to search the missing file a strong search command is required. The Linux Find Command is one of the most... Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 2322 days agogithub.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...Raghava's Group
Raghava's group is known for developing open source software or web servers. Group have developed large number of web-based services. Find more at http://www.imtech.res.in/raghava/-
Tools to Predict the Impact of Missense Variants !
Last updated 2966 days ago by JitPrioritizing missense variants for further experimental investigation is a key challenge in current sequencing studies for exploring complex and Mendelian diseases. A large number of in silico tools have been employed for the task of...
