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HOMER: Software for motif discovery and next-gen sequencing analysis
By Neel 3126 days agohomer.salk.edu - This tutorial covers topics independently of HOMER, and represents knowledge which is important to know before diving head first into more advanced analysis tools such as HOMER. Setting up your computing environment Retrieving and storing...Smash: An alignment-free method to find and visualise rearrangements between pairs of DNA sequences
By Jit 3125 days agobioinformatics.ua.pt - Smash is a completely alignment-free method/tool to find and visualise genomic rearrangements. The detection is based on conditional exclusive compression, namely using a FCM (Markov model), of high context order (typically 20). For...Painless package development for R
By Abhi 3118 days agowww.rstudio.com - Devtools makes package development a breeze: it works with R’s existing conventions for code structure, adding efficient tools to support the cycle of package development. With devtools, developing a package becomes so easy that it will be...Bioinformatics Tutor at PGIMER
Postgraduate Institute of Medical Education and Research (PGIMER) - Chandigarh, Chandigarh ₹9,300 - ₹34,800 a month Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh invites Online Applications for recruitment of...Summer internship positions at DuPont
DuPont Industrial Biosciences has several summer internship positions for undergrads available. We are looking for driven and creative interns to conduct research in the following areas: · Enzyme immobilization supports for select enzyme...
SLURM basics !
Last updated 3109 days ago by Radha Agarkar Comments (1)SLURM is a queue management system and stands for Simple Linux Utility for Resource Management. SLURM was developed at the Lawrence Livermore National Lab and currently runs some of the largest compute clusters in the world. SLURM is similar in...SATSUMA : Highly sensitive whole-genome synteny alignments.
By Jit 3108 days agosatsuma.sourceforge.net - Satsuma is a whole-genome synteny alignment program. It takes two genomes, computes alignments, and then keeps only the parts that are orthologous, i.e. following the conserved order and orientation of features, such as protein coding genes,...Hagfish - assess an assembly through creative use of coverage plots
By Abhi 3101 days agogithub.com - Hagfish is a tool that is to be used in data analysis of Next Generation Sequencing (NGS) experiments. Hagfish builds on the concept of coverage plots and aims to assist (amongst others) in quality control of de novo genome assembly or...Stampy
By Abhi 3101 days agowww.well.ox.ac.uk - Stampy is a package for the mapping of short reads from illumina sequencing machines onto a reference genome. It's recommended for most workflows, including those for genomic resequencing, RNA-Seq and Chip-seq. Stampy excels in the mapping of...mafTools
By Radha Agarkar 3100 days agogithub.com - Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.
