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FinisherSC: a repeat-aware and scalable tool for upgrading de novo assembly using long reads
By Jit 2826 days agokakitone.github.io - FinisherSC, a repeat-aware and scalable tool for upgrading de novo assembly using long reads. Experiments with real data suggest that FinisherSC can provide longer and higher quality contigs than existing tools while maintaining high...CLgenomics
By Radha Agarkar 2822 days agochunlab.wordpress.com - CLgenomics is a standalone desktop software specifically designed for bacterial genome analysis. This program has a powerful multi-genome browser, which enables rapid and responsive exploration of bacterial genomes. To use CLgenomics, individual...CONCOCT: Clustering cONtigs with COverage and ComposiTion
By Jit 2819 days agogithub.com - A program for unsupervised binning of metagenomic contigs by using nucleotide composition, coverage data in multiple samples and linkage data from paired end reads. Warning! This software is to be considered under development. Functionality and the...SeqMule: Automated human exome/genome variants detection
By Abhimanyu Singh 2818 days agoseqmule.openbioinformatics.org - SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its...UpSetR Shiny App!
By Jit 2780 days agogehlenborglab.shinyapps.io - UpSetR generates static UpSet plots. The UpSet technique visualizes set intersections in a matrix layout and introduces aggregates based on groupings and queries. The matrix layout enables the effective representation of associated data, such...CLA: Contig-Layout-Authenticator
By Jit 2759 days agojournals.plos.org - To improve upon the shortcomings associated with the construction of draft genomes with Illumina paired-end sequencing, we developed Contig-Layout-Authenticator (CLA). The CLA pipeline can scaffold reference-sorted contigs based on paired reads,...DeepVariant : an analysis pipeline that uses a deep neural network to call genetic variants from...
By Jit 1764 days agogithub.com - DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data. DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation...Bactopia: a flexible pipeline for complete analysis of bacterial genomes
By Abhi 168 days agobactopia.github.io - Bactopia is a flexible pipeline for complete analysis of bacterial genomes. The goal of Bactopia is process your data with a broad set of tools, so that you can get to the fun part of analyses quicker! Bactopia was inspired by Staphopia, a...multiPhATE: bioinformatics pipeline for functional annotation of phage isolates
By Abhimanyu Singh 2019 days agogithub.com - multiple-genome Phage Annotation Toolkit and Evaluator (multiPhATE). multiPhATE is a throughput pipeline driver that invokes an annotation pipeline (PhATE) across a user-specified set of phage genomes. This tool incorporates a de...Amity University Bioinformatics Summer Program - Kolkata
By eliabrodsky 1992 days agoRegistrations are now open for the 2019 Summer Bioinformatics Training program at Amity University, Kolkata.
