BioStar
Bioinformatician
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LASTZ
By Abhi 3859 days ago Comments (2)www.bx.psu.edu - LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS sequencing technologies such as...Smash: An alignment-free method to find and visualise rearrangements between pairs of DNA sequences
By Jit 3851 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...Edanchin Lab
My main topics of interest are: The impact of non tree-like evolution such as horizontal gene transfers and hybridization on species biology Evolution and adaptation of animals in the absence of sexual reproduction and the underlying...Professor/Senior Lecturer of Comparative Genomics @ University of Glasgow
University of Glasgow College of Medical, Veterinary and Life Sciences School of Biodiversity, One Health and Veterinary Medicine Professor/Senior Lecturer of Comparative Genomics Vacancy Ref: 153610 Salary: Professor, Grade 10 will be within...SATSUMA : Highly sensitive whole-genome synteny alignments.
By Jit 3834 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,...PRISM
By Jit 3623 days agocompbio.cs.toronto.edu - PRISM is a software for split read (reads which span across a structrual variant -- SV ) mapping and SV calling from the mapping result. PRISM is able to detect small insertions and abitrary size deletions, inversions and tandom duplications with...The Day We Began Reading the DNA of the World
By Jitendra Narayan 67 days agoImagine waking up one day and realizing that somewhere in a laboratory, a scientist is reading the DNA of a whale. Somewhere else, another team is sequencing a rare plant, while researchers in India are decoding the genomes of diverse human...dcGOR
By Martin Jones 4386 days agoan R package for analysing ontologies and protein domain annotationsCANU: Assembling Large Genomes with Single-Molecule Sequencing and Locality Sensitive Hashing.
By Jit 3851 days ago Comments (2)github.com - Canu is a fork of the Celera Assembler designed for high-noise single-molecule sequencing (such as the PacBio RSII or Oxford Nanopore MinION). The software is currently alpha level, feel free to use and report issues encountered. Canu is...
