Jit
Enthusiast computational biologist with business dream !!!
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Caretta – A multiple protein structure alignment and feature extraction suite
By Rahul Nayak 1905 days agowww.bioinformatics.nl - Caretta – a multiple protein structure alignment and feature extraction suite Caretta, a multiple structure alignment suite meant for homologous but sequentially divergent protein families which consistently returns accurate alignments...Mulan: MUltiple sequence Local AligNment and conservation visualization tool
By Rahul Nayak 3152 days agomulan.dcode.org - Mulan performs multiple (2 or more) sequence alignments with an efficient and rapid "full local" alignment strategy that ensures a recapitulation of evolutionary sequence rearrangements (such as inversions and reshuffling) in any of the species. It...PureCN: copy number calling and SNV classification using targeted short read sequencing
By Jit 2767 days agobioconductor.org - This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with...VGSC: A Web-Based Vector Graph Toolkit of Genome Synteny and Collinearity
By Abhimanyu Singh 2685 days agowww.ncbi.nlm.nih.gov - VGSC, the Vector Graph toolkit of genome Synteny and Collinearity, and its online service, to visualize the synteny and collinearity in the common graphical format, including both raster (JPEG, Bitmap, and PNG) and vector graphic (SVG, EPS, and...String graph based genome assembly software and tools !
By Rahul Nayak 3000 days agoIn graph theory, a string graph is an intersection graph of curves in the plane; each curve is called a "string". String graphs were first proposed by E. W. Myers in a 2005 publication.wtdbg2: A fuzzy Bruijn graph approach to long noisy reads assembly
By BioStar 2588 days agogithub.com - Wtdbg2 is a de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies (ONT). It assembles raw reads without error correction and then builds the consensus from intermediate assembly...Common steps for reads mapping !
By BioStar 1094 days agoMapping reads to a reference genome is an essential step in many types of genomic analysis, such as variant calling and gene expression analysis.ForBio and UiB course: Introduction to phylogenetic methods
By Rahul Nayak 2273 days agoThe is an introductory course that is aimed at students who will need to preform phylogenetic analyses in their work, but who have little or no experience with phylogenetic analyses.Steps to find palindrome in genomes !
By BioStar 1094 days agoPalindromes are sequences of nucleotides that read the same backward as forward.
